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Corrigendum: Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor indicates a cell-specific response that promotes CD44 activation
Dorota Piekna-Przybylska1
Daxiang Na1
Jingyuan Zhang2†
Cameron Baker3
John M. Ashton3
Patricia M. White1*- 1Department of Neuroscience, University of Rochester School of Medicine and Dentistry, Rochester, NY, United States
- 2Department of Biology, University of Rochester, Rochester, NY, United States
- 3Genomic Research Center, University of Rochester School of Medicine and Dentistry, Rochester, NY, United States
Hearing loss caused by the death of cochlear hair cells (HCs) might be restored through regeneration from supporting cells (SCs) via dedifferentiation and proliferation, as observed in birds. In a previous report, ERBB2 activation in a subset of cochlear SCs promoted widespread down-regulation of SOX2 in neighboring cells, proliferation, and the differentiation of HC-like cells. Here we analyze single cell transcriptomes from neonatal mouse cochlear SCs with activated ERBB2, with the goal of identifying potential secreted effectors. ERBB2 induction in vivo generated a new population of cells with de novo expression of a gene network. Called small integrin-binding ligand n-linked glycoproteins (SIBLINGs), these ligands and their regulators can alter NOTCH signaling and promote cell survival, proliferation, and differentiation in other systems. We validated mRNA expression of network members, and then extended our analysis to older stages. ERBB2 signaling in young adult SCs also promoted protein expression of gene network members. Furthermore, we found proliferating cochlear cell aggregates in the organ of Corti. Our results suggest that ectopic activation of ERBB2 signaling in cochlear SCs can alter the microenvironment, promoting proliferation and cell rearrangements. Together these results suggest a novel mechanism for inducing stem cell-like activity in the adult mammalian cochlea.
1. Introduction
Lost auditory hair cells (HCs) in adult mammals cannot be regenerated, driving permanent hearing loss. Conversely, lost HCs in birds are regenerated through the proliferation of supporting cells (SCs) and new HC differentiation (Corwin and Cotanche, 1988; Ryals and Rubel, 1988), leading to the restoration of hearing (Ryals et al., 2013). Limited regenerative capacity in the organ of Corti is also observed in newborn mammals and is associated with a pool of progenitor cells in the cochlear sensory epithelium (Atkinson et al., 2015; Zhang et al., 2020). These include a subset of SCs in proximity to HCs, such as inner border cells (IBC), inner pillar cells (IPC), the third-row Deiter cells (DC), and lateral greater epithelial ridge (LGER) (Chai et al., 2011; Shi et al., 2012; Kubota et al., 2021). Studies focusing on signaling pathways in mice that drive HC regeneration prior to hearing onset suggest that HC may regenerate through mitotic division followed by differentiation, via WNT signal activation (Chai et al., 2012; Shi et al., 2012, 2014). Alternatively, HCs may regenerate from progenitor cells by direct trans-differentiation, by blocking NOTCH signaling (Yamamoto et al., 2006; Korrapati et al., 2013; Mizutari et al., 2013; Bramhall et al., 2014). As maturation progresses, cochlear cells become restricted from both mechanisms of regeneration (Brown and Groves, 2020). These findings have been interpreted to mean that even limited regeneration capacity is lost from the adult mammalian cochlea. Notably, progenitors for HC-like cells may arise from proliferating cells in sphere cultures from adult human utricular tissue, but not adult cochlear tissues (Senn et al., 2020). Nonetheless, these findings do not rule out the possibility that quiescent adult mammalian cochlear progenitors exist (Hoa et al., 2020), but require a different microenvironment to manifest their potential.
Hearing restoration in birds occurs regardless of the age. Early studies showed that signaling through phosphoinositide 3-kinase (PI3K) and the epidermal growth factor receptor (EGFR) family are required for inner ear SC proliferation in both chicken and neonatal mice (Witte et al., 2001; White et al., 2012). Other studies on avian regeneration have implicated VEGF activation, which also signals through PI3K (Matsunaga et al., 2020; Wan et al., 2020). In the EGFR family, there are four closely related receptor tyrosine kinases: ERBB1, ERBB2, ERBB3, and ERBB4. These form homo or heterodimers with each other upon binding of the ligand and inducing molecular pathways SCs proliferation, migration and survival. We previously showed that signaling mediated by ERBB2, which is the preferred heterodimerization partner for the other three EGFR family members, drives proliferation of SCs in explant cultures and supernumerary HC-like formation in vivo in the neonatal mouse cochlea (Zhang et al., 2018). Notably, in those studies, lineage tracing revealed that cells expressing constitutively active (CA) mutant form of ERBB2 induced these activities in neighboring cells, suggesting the presence of an amplifying signal cascade that recruits adjacent tissue. Consistent with this interpretation, SOX2 protein was broadly down-regulated in the apical turn harboring sparse CA-ERBB2 + cells (Zhang et al., 2018).
To identify ERBB2-mediated signaling pathways associated with the changes in SCs that may facilitate HC regeneration, we performed single cell RNA sequencing (scRNA-seq) on sorted neonatal SCs with and without CA-ERBB2. We performed cluster-specific gene analysis to identify differentially expressed genes (DEGs) in different cell populations. Our goals were to identify clusters of CA-ERBB2 cells that are transcriptionally distinct, assign clusters and DEGs to SC subtypes and identify candidate secondary signaling pathways that could act downstream of ERBB2 signaling to promote local changes. We further sought to confirm if selected downstream mediators were also expressed in the cochlea of young adult mice after damage and CA-ERBB2 activation, and if so, where they were located.
2. Materials and methods
2.1. Ethical approval
All experiments using animals were approved in advance by the University Committee on Animal Research (UCAR) at the University of Rochester, protocol number 2010-011, PI Patricia White, and by the Animal Care and Use Review Office (ACURO) of the Department of Defense.
2.2. Mice
The following mouse strains were used. Fgfr3-iCre (Cox et al., 2012) was a kind gift from Dr. Jian Zuo. TetON-CA-ErbB2 (Xie et al., 1999) and CBA/CaJ, were purchased from Jackson Laboratories. ROSA-floxed-rtTA/GFP (Belteki et al., 2005) was a kind gift from Dr. Lin Gan. TetON-CA-ErbB2 mice harbor a mutated ErbB2 transgene encoding a CA ERBB2 protein (CA-ERBB2), which does not require ligand binding or heterodimerization with other ERBB partners for active signaling. Fgfr3-iCre and TetON-CA-ERBB2 mice were crosses to generate double heterozygous transgenic mice that were subsequently used as breeders. In a second breeding, double heterozygous were crossed with homozygous ROSA-floxed-rtTA/GFP mice.
2.3. Genotyping
For scRNA-seq experiments and data validation by RT-qPCR, generated pups were genotyped at P0 to identify triple-transgenic mice that harbor Fgfr3-iCre, ROSA-floxed-rtTA/Gfp, and TetON-CA-ErbB2 (named here as CA-ERBB2). The pups were not genotyped to identify sex. Oligonucleotides used in genotyping are provided in Supplementary Table 2. Littermates with both Fgfr3-iCre and ROSA-floxed-rtTA/Gfp were used as Controls.
2.4. Noise exposure
For scRNA-seq data validation in young adults exposed to noise, both male and female mice were used equally. Mice harboring the Fgfr3-iCre and CA-Erbb2 transgenes have been backcrossed to CBA/CaJ for at least four generations, whereas the ROSA-rtTA-GFP line is congenic on C57BL6/J. Thus, the experimental mice are hybrid CBA/C57 mice, whose noise damage characteristics are similar to a pure CBA/CaJ response (Milon et al., 2018). Three-week-old mice were genotyped and weaned. Tamoxifen injections (75 mg/kg) were performed at P21, P22, and P23. At P28 their hearing was tested by auditory brainstem response (ABR) and distortion product acoustic emissions (DPOAE) (Zhang et al., 2021). The mice were then divided into DOX exposed and control conditions. Mice experienced a noise exposure of 110 dB of 8–16 kHz octave band noise for 2 h, as described previously (Zhang et al., 2021). The next day (1 DPN), mice received hearing tests to confirm severe noise-induced hearing loss evident by threshold shift for at least 25 dB across five frequencies (8, 12, 16, 24, and 32 kHz). Two days later (3 DPN), the DOX group were injected with DOX (100 mg/kg), followed 30 min later by an injection of furosemide (400 mg/kg) (Walters and Zuo, 2015). The control group received a saline injection, followed by furosemide. Two days after these injections (5 DPN), the mice were euthanized and their cochleae fixed overnight in fresh 4% paraformaldehyde. A second cohort of mice were treated identically, except that they also received 2 injections of 10 mg/kg 5-ethynyl-2′-deoxyuridine (EdU) from the Click-iT EdU Alexa Fluor 647 imaging kit (Invitrogen, Carlsbad, CA, USA), the day after DOX injection (4 DPN) spaced 8 h apart. These mice were euthanized on 7 DPN and their cochleae were fixed overnight in fresh 4% paraformaldehyde.
2.5. Cell dissociation and FACS sorting
The iCRE activity was induced by tamoxifen injections (75 mg/kg) at P0/P1 to label SCs with GFP and rtTA. Doxycycline injections (100 mg/kg) were performed at P2 to drive CA-ERBB2 expression in GFP + SCs. Cochlea from P3 pups were collected and incubated with 1 mL Accutase® solution (Innovative Cell Technologies) for 15 min at 37°C. To ensure a reproducible digestion, 2–4 cochlea were treated per tube. The Accutase solution was removed and cochlea were gentle washes in ice cold Ca2 +, Mg2 + free HBSS buffer. Organs in each tube were dissociated by trituration for 2–3 min. Cells were then filtered with a 40 μm cell strainer (BD Biosciences) and kept on ice until sorted. For the exclusion of dead cells and debris from the samples during sorting, a single-cell suspension was stained with DAPI. Sorting was performed at 4°C in a FACSAria II cell sorter (BD Biosciences) using a 130 μm nozzle. Scatter discrimination was used to eliminate doublets and samples were negatively selected with DAPI to remove dead cells and debris. For scRNA-seq, single GFP + cells were captured into 96-well plate with 11.5 μl lysis buffer and RNase Inhibitor without the CDS IIA Oligo (Takara Bio, Mountain View, CA, USA), and stored at −80°C until used for construction of cDNA libraries. On average, six pups per genotype were processed for sorting single GFP + cells into one 96-well plate. For data validation by RT-qPCR, GFP + cells were captured into single tube with 100 μl lysis buffer containing Proteinase K and DNase (Bio-Rad). The sorted cells were then incubated for 10 min. in room temperature, followed by 5 min. at 37°C, and 5 min. at 75°C. The samples were stored at −80°C until RT-qPCR analysis.
2.6. Construction of single-cell RNA-seq libraries
Single-cell RNA-seq libraries were constructed according to the SMART-Seq Single PLUS protocol (Takara Bio, Mountain View, CA, USA). Frozen plates were thawed on ice. Next, cDNA was generated with the addition of the 3′ SMART-Seq CDS Primer II A and SMARTScribe II RT reagents. cDNA was amplified via 20 cycles of PCR, purified, and assessed for quantity and quality by Qubit dsDNA assay (Thermo Fisher Scientific, Waltham, MA, USA) and Fragment Analyzer (Agilent, Santa Clara, CA, USA) analysis, respectively. For each well, 1 ng amplified cDNA was fragmented and prepared for library construction with the addition of stem-loop adapters. Final library amplification and indexing was performed through 16 cycles of PCR amplification. Following bead purification, individual library profiles were assessed by Fragment Analyzer and quantified by Qubit dsDNA assay. Libraries were diluted, pooled in equimolar amounts, and sequenced on a NovaSeq S1 flowcell (Illumina, San Diego, CA, USA) to generate an average of 10 million reads per cell.
2.7. Data preprocessing, clustering, and visualization
Raw reads generated from the Illumina basecalls were demultiplexed using bcl2fastq version 2.19.1. Quality filtering and adapter removal are performed using FastP version 0.20.1 with the following parameters: “–length_required 35 –cut_front_window_size 1 –cut_front_mean_quality 13 –cut_front –cut_tail_window_size 1 –cut_tail_mean_quality 13 –cut_tail -y -r.” Processed/cleaned reads were then mapped to the Mus musculus reference genome (GRCm38 + Gencode-M25 Annotation) using STAR_2.7.6a with the following parameters: “—twopass Mode Basic –runMode alignReads –outSAMtype BAM SortedByCoordinate—outSAMstrandField intronMotif –outFilterIntronMotifs RemoveNoncanonical –outReads UnmappedFastx.” Gene level read quantification was derived using the subread-2.0.1 package (featureCounts) with a GTF annotation file (Gencode M25) and the following parameters: “-s 2 -t exon -g gene_name.” The data generated by the sequencing was used to create a Seurat object using the Seurat package in R (v4.0.5 and v4.1.2). Quality control metrics were performed using standard Seurat (v4.0.4 and v4.1.0) protocols and included the identification of unique genes (“features”) per cell, the total number of molecules detected (“reads”), and the percent of mitochondrial genome contamination. The data was normalized. Clusters were identified with the Louvain method, using PCA and UMAP to reduce dimensionality and plot the cells. Clustering was performed using a dimensionality reduction of 1:30 and two separate resolutions, 0.2 and 0.6, within the Nearest-neighbor graph construction and UMAP generation. In addition to performing sample filtering and clustering, Seurat handled differential expression to determine genes up-regulated within clusters and across condition groups. enrichR (v3.0) was used to perform gene set enrichment on DEGs (Xie et al., 2021). A final report was rendered using Rstudio and rmarkdown (v2.10). Identity of genes was analyzed in the Gene Ontology (GO) resource1 (Xie et al., 2021). GO biological process analysis was performed for up-expressed genes identified in each cluster. Since there were to many up-expressed genes for some of the clusters we limited the number of markers coming from specific clusters based on log-fold change. The log-fold change threshold for cluster S7 was 4, for cluster S0 was 4, and for cluster S5 was 6. The log-fold change threshold for the remaining clusters remained at 2. The protein interaction network modules were visualized using STRING network online analysis2 (Szklarczyk et al., 2021).
2.8. RT-qPCR analysis
Cell lysates prepared after sorting GFP + cells into single tube were used in RT-qPCR analysis using SingleShot Two-Step RT-qPCR reagents (Bio-Rad) according to manufacture instruction. Each qPCR reaction was performed on cells lysates corresponding to 10 cells. Three technical replicates were used for each analyzed gene. Wells with primers but without cDNA sample were utilized for negative controls, while cell lysates not treated with reverse transcriptase were used as a control of genomic DNA contamination. qPCR reactions were performed using Bio-Rad CFX Thermal Cycler and the threshold of cycles (Ct) values was calculated with Bio-Rad CFX Manager Software. ΔΔCt method was used for calculating relative gene expression. Eef1a1 and Tubb4a were previously tested and indicated as stable expressing housekeeping genes adequate for normalization (Park et al., 2016), and were used here as reference genes to calculate differences in gene expression between Control and CA-ERBB2 cells. The Ct values of technical replicates were averaged and expression of the gene in CA-ERBB2 sample and Control sample was normalized to reference gene (“REF”) expression level within the same sample to determine ΔCt [Ct (gene)—Ct (REF)]. For each gene, analysis of relative gene expression was performed from at least three biological samples (three independent FACS sortings). The ΔCt for each biological replicate was exponentially transformed to the ΔCt expression (2–ΔCt) before averaging and determining the standard deviation (SD). The mean was then normalized to the expression of gene in Control sample to find ΔΔCt expression in CA-ERBB2 sample. Oligonucleotides used in RT-qPCR are provided in Supplementary Table 2.
2.9. Immunochemistry
Fixed cochleae were decalcified in 100 mM EDTA in a saline solution at 4°C for 3 days. For cryosectioning, tissues were immersed in 30% sucrose in PBS overnight, embedded in OCT, frozen in liquid nitrogen, and cryosectioned at 20 microns. Sections were mounted on slide glass and kept at −30°C until use. Immunostaining of cryostat cochlear sections was performed to examine the expression of selected genes. The sections were permeabilized and blocked in PBS with 0.5% Triton X-100 and 5% donkey serum (TDB buffer) for 1 h at 4°C, followed by incubation with primary antibodies in TDB at 4°C overnight. The sections were rinsed briefly four times in PBS, then incubated with secondary antibodies in TDB at 4°C overnight. The sections were rinsed briefly 4 times in PBS. The following primary antibodies were used: chicken anti-GFP (1:100; Abcam; AB_300798), mouse anti-PVALB (1:1,000, EMD Millipore; MAB1572), goat anti-OPN (SPP1; 1:100; R&D Systems; AF808), goat anti-TIMP1 (1:100; R&D Systems; AF980), rabbit anti-CD44 (1:100; Abcam; AB157107), rabbit anti-pERBB2 (1:200; Santa Cruz; sc-12352), goat anti-SOX2 (1:500; Santa Cruz; sc-17320), rabbit anti-MYO7 (1:1,000; Proteus; 25-6790), rabbit anti-activated CASP3 (1:500; R&D Systems, AF835), and rabbit anti-TAK1 (1:500; Thermo Fisher Scientific; 28H25L68). Secondary antibodies were purchased from Jackson Immunoresearch. EdU was revealed using the Click-iT EdU Alexa Fluor 647 kit (Invitrogen; C10340) following the manufacturer’s instructions. Imaging was performed using Confocal Microscope Olympus FV1000.
3. Results
3.1. Experimental design to determine transcriptome of cochlear SCs expressing ERBB2
To perform scRNA-seq analysis of SCs expressing ERBB2, we employed the same genetic mouse model that revealed an indirect effect of ERBB2 activation on SOX2 expression and the formation of ectopic HC-like cells (Supplementary Figure 1; Zhang et al., 2018). These mice harbor an inducible mutated ErbB2 transgene encoding CA-ERBB2. In order to limit activation of CA-ERBB2 to SCs, we used an inducible DNA Cre recombinase under control of the SC gene promoter Fgfr3 (Supplementary Figure 2; Cox et al., 2012). Double heterozygotic mice (“Tet-On” CA-ErbB2, Fgfr3-iCre) were then bred to homozygous line harboring a “floxed” TA transcription factor, with an IRES-GFP to use as a lineage marker (“ROSA-rtTA-Gfp”). The resulting pups with CA-ErbB2 and Fgfr3-iCre (denoted here as “CA-ERBB2”) were used to analyze the transcriptome of SCs with induced ERBB2 signaling; whereas pups harboring Fgfr3-iCre were used as “Control.” Activation of iCRE was performed by two injections of tamoxifen at P0 and P1, which resulted in GFP expression to label SCs (Supplementary Figure 1). CA-ERBB2 expression was induced at P2 by doxycycline injection. The organs of Corti were dissected from P3 pups, and living GFP + SCs were purified by fluorescence-activated cell sorting (FACS) by excluding cells that had taken up a cell-impermeant dye (Supplementary Figure 2). On average, we obtained 55 ± 13 GFP + cells per cochleae. RNA cDNA libraries were prepared and sequenced from about 300 GFP + single cells per genotype collected in three independent FACS experiments with 85% cells having less than 20% mitochondrial transcript expression (Supplementary Figure 3).
3.2. New populations of transcriptionally distinct cochlear cells arise in response to ERBB2 signaling
Quality control metrics revealed similar numbers of transcripts and UMI counts for the two genotypes (Figure 1A). A preliminary UMAP plot of all of the cells revealed intermingling of CA-ERBB2 and Control cells as well as evidence for their separate differentiation (Figure 1A, right). Unbiased clustering (clustering resolution of 0.2) was then used to group all GFP + cells prior to assessment of transcriptome changes associated with CA-ERBB2 expression. Based on the pattern of gene expression, FACS-purified GFP + cells can be grouped into at least 5 clusters (Figures 1B, C). Two clusters showed significant differences between Control and CA-ERBB2 samples in distribution of cochlear cells: cluster C4, mostly comprised of Control cells, and cluster C3 formed entirely by CA-ERBB2 cells. Significant changes in the cell distribution were also observed within cluster C2, where CA-ERBB2 cells have clearly segregated away from Control cells. There were no differences between Control and CA-ERBB2 in distribution of cochlear cells in clusters C0 and C1. These results suggest heterogeneity in the responses of SCs to intrinsic ERBB2 activation. In a minority of GFP + cells, ERBB2 activation drove a greater transcriptional response, one that differentiated the activated cells away from the parent population.
FIGURE 1
Figure 1. Unbiased Seurat clustering of cochlear SC transcriptomes from control and CA-ERBB2 samples. (A) Violin plots showing similar distributions observed for cells from control and CA-ERBB2 samples in the number of detected transcripts per cell and in UMI counts per cell used in generating sequencing libraries. On the right, preliminary UMAP plot showing distribution of CA-ERBB2 cells and control cells. Populations of CA-ERBB2 cells that shifted away from control cells are depicted by dotted line. (B) Initial unbiased clustering showing differences between control cells and CA-ERBB2 cells in the number of clusters and in distribution of cells within the clusters. On right, bar graph showing proportion of control and CA-ERBB2 cells found in each cluster. (C) A second unbiased clustering distinguishes subpopulations within clusters C0, C1, and C2, generating ten unique clusters (S0–S9) with two clusters formed by CA-ERBB2 cells only (S4 and S7) and two clusters mostly composed of Control cells (S2 and S5). On right, bar graph showing proportion of Control and CA-ERBB2 cells found in each cluster. Statistical analyses were performed with Seurat package in R version 4.1.2.
To better understand the transcriptional diversity of cochlear SC with induced ERBB2 signaling, we performed unbiased clustering (clustering resolution of 0.6) that resulted in distinguishing subpopulations within clusters C0, C1, and C2. Ten unique clusters (S0–S9) were generated with two clusters composed of CA-ERBB2 cells only (Figure 1C). Notably, in addition to cluster S4 that corresponds to C3 in first unbiased clustering, CA-ERBB2 cells in cluster C2 were distinguished as cluster S7. Most of remaining cells in cluster C2 were Control cells (∼80%) and were identified as cluster S2. Another cluster represented mostly by Control cells (∼90%) is S5, which corresponds to C4 in the first unbiased clustering. In remaining clusters, distribution of Control and CA-ERBB2 cochlear cells was similar.
3.3. Assignment of SC subtypes to clusters
To assess which SCs contributed to which clusters, we graphed expression of genes specific to SC subtypes, as described for scRNA-seq of P1 SCs (Kolla et al., 2020; Supplementary Table 1 and Supplementary Figure 4). At birth, Fgfr3-iCre can be expressed in DC, inner and outer pillar cells (IPC, OPC), outer hair cells (OHC), and Hensen cells (HeC). In our system, Fgfr3-iCre expression is sparser, and expression in HC, DC, and HeC is biased toward the apical region, where cells are less differentiated (Supplementary Figure 2). Here we used the 5-cluster analysis, as we anticipated a similar number of cell types. Results in Figure 2 show that the HC markers Ccer2, Pvalb, and Insm1 are clustered together in a subset of C2 (Figures 2B, C). The HeC marker Fst is expressed in C1, whereas Nupr1 is present in both C1 and C2 (Figures 2B, D). All five DC markers, Hes5, Pdzk1ip1, S100a1, Prss23, and Lfng, were most strongly up-regulated in C2 (Figures 2B, E). PC makers were more ambiguous, but were most up-regulated also in C2 (Figures 2B, F). C4, which is comprised primarily of Control cells, expressed all markers examined at a moderate level and thus could not be identified. C0 is a mix of CA-ERBB2 and Control cells, and it expresses a handful of sensory-specific markers, which were S100a1, S100b, and Cryab. Its identity is likewise ambiguous. C3 is composed exclusively of CA-ERBB2 cells and primarily expresses OPC markers (Figures 2B, F, note Smagp levels). However, it also contains identifying markers for LGER1 (LGER group 1), such as Dcn, Ddost, Pdia6, Rcn3, and Sdf2l1. These are also enriched in C1 and C2 (Figure 2G).
FIGURE 2
Figure 2. UMAP plots and violin plots for marker gene transcripts identifying cochlear cells. (A) Schematic cross-section of the cochlear duct showing the position of different cell types. IHC, inner hair cells; OHC, outer hair cells; GER, greater epithelial ridge; IBC, inner border cells; IPH, interphalangeal cells; IPC, inner pillar cells; OPC, outer pillar cells; DC, Deiter cells; HeC, Hensen cells. (B) Cluster plot from Figure 1B, with putative cell type designations. (C) Three HC markers are presented: Ccer2, Pvalb, and Insm1. (D) Two HeC markers are shown: Fst and Nupr1. (E) The following marker genes were used to identify Deiter cells: Hes5, Pdzk1ip1, S100a1, Prss23, Lfng. (F) Five markers for IPC and OPC are shown: Cryab, Emid1, Npy, S100b, and Smagp. (G) Lateral GER cells express Dcn, Ddost, Pdia6, Rcn3, Sdf2l1. The most informative markers were chosen for display. Cochlear SC identity associated with analyzed marker gene is indicated on UMAP plot. Expression of the HeC and OPC marker gene Fam159b, and the IHC marker gene Acbd7 were not detected.
3.4. A minority of CA-ERBB2 SCs are transcriptionally distinct from control SCs
Induction of ERBB2 signaling in CA-ERBB2 cells may result in activation of genes that normally are not expressed in cochlear SCs. Therefore, to identify DEGs between Control and CA-ERBB2 samples, we performed statistical analysis using both the Wilcoxon rank-sum test and the Likelihood-Ratio (LR) test. In the Wilcoxon rank-sum test, DEGs are identified among genes that have some level of expression in the compared conditions. The LR test allowed for detection of DEGs with undetectable expression within one condition (McDavid et al., 2013). Genes were mapped in the GO resource (Figure 3A). Sequences that could not be mapped to a corresponding protein record in the PANTHER classification system were designated “unmapped IDs.” They mostly represent non-coding RNAs and pseudogenes.
FIGURE 3
Figure 3. Analysis of DEGs in CA-ERBB2 cells and top up-expressed genes identified in cluster S4 and S7. (A) Graphical representation of statistically significant changes in gene expression between CA-ERBB2 SCs and control SCs. Graphs showing number of up- and down-regulated genes in CA-ERBB2 cells identified in Wilcoxon rank-sum test (top) and in likelihood-ratio test (bottom). In each group, protein coding transcripts are represented in gray, and non-coding RNA (ncRNA)/pseudogenes are represented in black. Numbers in bar indicate numbers of transcripts with mapped IDs (protein coding) and unmapped IDs (ncRNA/pseudogenes). On right, pie graphs for Wilcoxon rank-sum test (top) and likelihood-ratio test (bottom) showing the percentage of differentially expressed genes (DEG) found in up to 10% of cells, 10–20% of cells, 20–50% of cells, and in above 50% of cells. (B) Volcano plots showing the distribution of gene expression fold changes on the x-axis and p-values for DEGs on the y-axis identified in Wilcoxon rank-sum test (left) and likelihood-ratio test (right). Top up- and down-regulated genes with mapped IDs in the PANTHER classification system are indicated in the Wilcoxon rank-sum test volcano plot. Genes highlighted in yellow were unique to that test. Selected genes of interest are indicated in the likelihood-ratio test volcano plot. Complete list of genes is provided in Supplementary Tables 3, 4. (C) Dot plots showing the expression distribution of the top 30 genes of cluster S4 and S7 among all clusters. Darker dots have a greater expression level, whereas larger dots indicate that more cells expressed that gene. Complete list of up-expressed genes is provided in Supplementary Table 5. (D) Gene Ontology (GO) term enrichment analysis for up-expressed genes of cluster S4 and S7. Bar charts shows the top 10 enriched GO terms of biological process for S4 and S7, along with corresponding p-values (<0.05). An asterisk (*) next to a p-value indicates the term also has a significant q-value (<0.05). The y-axis represents biological process, and the horizontal axis represents the number of genes, which are listed on the left side of the graph. Complete list of terms is provided in Supplementary Table 6.
Using Wilcoxon rank-sum test (adj p < 0.05, logFC > 2), 584 DEGs were identified, with 68 genes up-regulated and 516 genes down-regulated (Supplementary Table 3). Around half of the genes in each group were unmapped IDs. Almost 90% of DEGs were found in less than 10% of the CA-ERBB2 population. Using the LR test (adj p < 0.05, logFC > 2), 1,556 DEGs were identified (Supplementary Table 4). A total of 1,049 genes were up-regulated, and 507 genes were down-regulated, and around half of them were protein coding genes (Figure 3A). About 64% of the DEGs were found in less than 10% of CA-ERBB2 population. Volcano plots were used to show DEGs for both analyses (Figure 3B). Note how the LR analysis enables the identification of very significant DEGs like Wnt10a (Figure 3B right).
In both analyses, Spp1 was among the most up-expressed genes (132-fold change) in about 80% of CA-ERBB2 cells, in comparison to expression of Spp1 in 55.4% of Control cells. Spp1 will be more fully described later. Lama3 was among the most down-regulated genes in CA-ERBB2 cells in both tests. It was detected in 3.4% of CA-ERBB2 cells, compared to 23.2% of Control cells. LAMA3 is a subunit of laminins, which mediate the attachment, migration and organization of cells by interacting with integrin receptors and other extracellular matrix (ECM) components (Belkin and Stepp, 2000; Hamill et al., 2010). In the LR test, Kyphoscoliosis peptidase (Ky) gene is top differentially expressed (3530-fold change), but only in about 7.3% of CA-ERBB2 cells, in comparison to 21.5% of Control cells. KY’s proposed function is maintenance of cytoskeleton and neuromuscular junction (Hedberg-Oldfors et al., 2016). These data suggest that some CA-ERBB2 cells modify the local environment, potentially affecting the behavior of neighboring cells.
To better understand transcriptional heterogeneity among CA-ERBB2 cells in clusters S4 and S7, we identified up-regulated genes in each cluster described in Figure 1C, and then examined activated pathways against the GO biological process database. For each of 10 clusters, we analyzed gene expression in comparison to remaining clusters. Using the criteria of an adjusted p-value of < 0.05 and a difference in levels of expression greater than twofold, we found 90 genes up-expressed in cluster S4, and 1102 genes in cluster S7. The expression of thirty top up-expressed genes identified in clusters S4 and S7 in comparison to other clusters is shown in Figure 3C. For the remaining clusters, which are composed of Control and CA-ERBB2 cells (except cluster S5), we found that S0 had 1125 up-expressed genes, S1–810, S2–731, S3–359, S5–3722, S6–484, S8–426, and S9–144 (Supplementary Table 5). The top 10 up-expressed genes in each cluster were then used to generate heatmaps (Supplementary Figure 5).
The analysis revealed that among top up-expressed genes in cluster S4 are DEGs identified in Wilcoxon rank-sum test (Spp1, CD63, Tmsb4x; Figure 3B and Supplementary Table 3), and in the LR test (Spp1, Timp1, Dmp1, Mmp9, CD63; Figure 3B and Supplementary Table 4). According to the heatmap, S4 was not related to any other cluster (Supplementary Figure 5). In contrast, cluster S7, comprised of CA-ERBB2 cells only, had some up-regulated genes in common with top up-regulated genes in cluster S2, which was mostly Control cells. This suggests that CA-ERBB2 cells of cluster S7 originated from the same population as Control cells from cluster S2. Among the top up-expressed genes of S7 are DEGs identified in the LR test (Plet1os, Rufy4, Plet1, Cutal) (Figure 3B and Supplementary Table 4).
With respect to clusters comprised of both CA-ERBB2 and Control cells, some transcriptional relationships were also evident (Supplementary Figure 5). For example, cluster S6 had similarities to cluster S1, which is in proximity on the UMAP analysis. There were no marker genes up-expressed in cluster S0, S3, and S5. Surprisingly, in cluster S5 composed mostly of Control cells some level of up-regulation was observed for most of the up-expressed genes identified in other clusters, with exception of genes in cluster S8. Finally, clusters S8 and S9 are represented by small number of cells with up-expressed genes generally not found in other clusters, indicating that they are transcriptionally distinct populations. This analysis underscores the diversity of responses by SCs to CA-ERBB2 expression.
In summary, CA-ERBB2 drove the greatest transcriptional changes in a minority of cells, presumed to be DCs and PCs. Cells responding to CA-ERBB2 altered expression of hundreds of distinct transcripts. We focused on these changes to identify correlates for the indirect effects of CA-ERBB2 expression on neighboring cells.
3.5. CA-ERBB2 cells express genes involved in modulation of extracellular matrix
Gene set enrichment analysis against GO biological process was performed for up-expressed genes of cluster S4 and S7 to identify molecular pathways responding to ERBB2 activation (Figure 3D). For other clusters, results with listed 10 top GO terms with significant q-value < 0.05 are in Supplementary Figure 6, and complete list of terms for all clusters is provided in Supplementary Table 6. Among the most enriched annotations, both by adjusted p-value and number of genes involved, were annotations of genes linked to modulation of ECM. The distinctive cluster S4, formed entirely by CA-ERBB2 cells, showed various degrees of activation of markers involved in extracellular matrix organization (GO:0030198), and extracellular matrix disassembly (GO:0022617). Cluster S4 had also enriched genes associated with cellular response to cytokine stimulus (GO:0071345), cytokine-mediated signaling pathway (GO:0019221) and regulation of integrin-mediated signaling pathway (GO:2001044). We note that clusters S1 and S6 were also distinguished by up-expressed genes involved in extracellular matrix organization and disassembly.
With respect to the distinctive cluster S7 of CA-ERBB2 cells, GO biological process analysis did not reveal terms with q-value < 0.05 (Figure 3D). However, among terms with significant p-value (<0.05), are terms associated with genes Krt17 and Plet1 listed as DEGs in the LR test (Figure 3B and Supplementary Table 4). Epidermis development (GO:0008544) is associated with Krt17 and Col7a1 genes. This term is in a parent-child relationship with the term related to HC differentiation (inner ear auditory receptor cell differentiation, GO:0042491). Moreover, Plet1 is associated with wound healing, the spreading of epidermal cells (both GO:0035313 and GO:0044319), and negative regulation of cell-matrix adhesion (GO:0001953) (Supplementary Table 6).
In clusters S1, S2, and S6, CA-ERBB2 cells were intermingled with Control cells suggesting that they have similar transcriptome. The identified GO terms for these clusters indicate that cochlear cells of P3 mice still undergo changes related to development of the organ of Corti (Supplementary Figure 6). For example, cells in cluster S1 were enriched of genes associated with sensory organ morphogenesis (GO:0090596), collagen fibril organization (GO:0030199), regulation of endothelial cell migration (GO:0010594), endodermal cell differentiation (GO:0035987), and skeletal system development (GO:0001501). In cluster S2, cells showed up-regulation of genes involved in epithelial cell development (GO:0002064), regulation of transcription involved in cell fate commitment (GO:0060850), and NOTCH signaling pathway (GO:0007219). In cluster S6, enriched genes are associated with sensory perception of mechanical stimulus (GO:0050954), and sensory perception of sound (GO:0007605).
Cells in cluster S8 were enriched of terms associated with cellular division. Analysis of transcriptomes for cell cycle-specific gene expression confirmed that cells in cluster S8 are in S and G2/M phase (Supplementary Figures 6, 7). The analysis also revealed that whereas most cells across the conditions were in G1 phase, clusters S4 and S0 also showed enrichment of cells in phase S and G2/M, indicating some cells prepared for, or underwent cell division (Supplementary Figure 7). In cluster S8, both CA-ERBB2 cells and Control cells showed markers for phase S and G2/M, however, in cluster S0 this population was mostly represented by CA-ERBB2 cells.
Taken together, these results indicate that the transcriptional changes induced by CA-ERBB2 cells include the de novo expression of cytokines and signaling pathway genes. Many are predicted to modulate the extracellular matrix and affect differentiation, promoting proliferation in a minority of cells.
3.6. The most highly up-regulated genes in CA-ERBB2 cells are predicted to form a protein network that modulates extracellular signaling
As one goal of this study was to identify candidate secondary signaling pathways that could act downstream of ERBB2 signaling, we focused next on the new population of CA-ERBB2 cells that formed a transcriptionally distinct cluster S4. Top up-regulated genes Spp1, Timp1, Mmp9, and Dmp1, are found in GO annotations associated with modulation of ECM and cytokine response (Figure 3D). Using STRING software, we analyzed protein-protein interaction network for SPP1, TIMP1, MMP9, and DMP1. The results are visualized in Figures 4A–D, and scores for predicted interactions are summarized in Table 1. The analysis shows that interactions between SPP1, TIMP1, MMP9, and DMP1 have association scores in the high and the highest confidence range (scores above 0.7 and 0.9, respectively). Increasing the network for additional five proteins revealed CD44 as protein with close association (Figure 4B), with the highest confidence score (above 0.9) calculated for SPP1, TIMP1, and MMP9, indicating likely true associations. Additional five proteins added to the network revealed two proteins that were found as differentially expressed between CA-ERBB2 and Control cells (Figure 4C). These proteins were CD63 and HPX, and both have association scores in the highest confidence range (above 0.9) with TIMP1; whereas HPX has also association score in the high confidence range (above 0.7) with MMP9.
FIGURE 4
Figure 4. STRING protein-protein interaction network of four top up-regulated genes in cluster S4. (A) Protein-protein interaction network connectivity among SPP1, TIMP1, MMP9, and DMP1. In (B, C) protein-protein networks are shown with increasing number of closely associated genes. An edge was drawn with colored lines representing a type of evidence used in predicting the associations. A purple line indicates experimental evidence; a light green line indicates text-mining evidence; a light blue line indicates database evidence; a black line indicates co-expression evidence; and a light violet line indicates protein homology. The score interactions are summarized in Table 1. In (D) UMAP plot with marked cluster S4 enriched in cells expressing Spp1, Timp1, Mmp9, and Dmp1 in response to induction of ERBB2 signaling. In (E) UMAP plots and split violin plots showing up-regulated expression of Spp1, Timp1, Mmp9, and Dmp1 in CA-ERBB2 compared to Control cells in different clusters. (F) RT-qPCR validation of scRNA-seq analysis performed on GFP + FACS-sorted cells from P3 cochleae. The level of gene expression in CA-ERBB2 sample is presented as ΔΔCt value (± SD) relative to control (CTRL) normalized against the expression of the two reference genes Eef1a1 (E) and Tubb4a (T) (n = 3). Significance (*p < 0.05; **p < 0.01) was determined by unpaired t-test (ONE–TAILED) analysis.
TABLE 1
Table 1. The combined score of interactions between pair of proteins in STRING database analysis.
SPP1 and DMP1 are small integrin binding n-linked glycoproteins (SIBLINGs), which are secreted ligands for CD44 and integrin αvβ3 receptors. They promote survival, proliferation, differentiation, and migration in different systems (Flores et al., 1992; Ashkar et al., 2000; Sodek et al., 2000; Denhardt et al., 2001; Jain et al., 2002; Karadag et al., 2005; Rangaswami et al., 2006; Kazanecki et al., 2007; Wu et al., 2011). TIMP1 inhibits MMP9, a metallopeptidase that modulates both CD44 (Visse and Nagase, 2003; Grunwald et al., 2019) and NOTCH signaling (Garg et al., 2010). The CD44 receptor has a role in cell survival and proliferation in cancer development, but a recent finding also highlights its important role in tissue regeneration and wound healing (Denhardt et al., 2001; Kyriakides et al., 2009; Kim et al., 2012; Michopoulou et al., 2020). Notably, CD44 is endogenously expressed on OPCs in mice in adulthood (Hertzano et al., 2010).
Analysis of UMAP and split violin plots for Spp1, Timp1, Mmp9, and Dmp1 indicates that up-expression of these genes is observed in CA-ERBB2 cells for most clusters, with significant enrichment in cluster S4 (Figure 4E). Control cells express lower levels of Spp1 and Timp1 genes, particularly in cluster S1, S5, and S6. For genes Mmp9 and Dmp1, almost no expression is detected in Control cells, except for cluster S9 and S5. To validate the scRNA-seq analysis, we performed reverse transcriptase quantitative polymerase chain reaction (RT-qPCR) on FACS-sorted cochlear GFP + cells collected from CA-ERBB2 and Control neonatal mice. Results of RT-qPCR analysis are shown in Figure 4F. They confirm that activation of ERBB2 signaling in CA-ERBB2 cells drove significant up-regulated expression of genes Spp1, Timp1, Mmp9, and Dmp1, and also other genes identified as up-expressed in CA-ERBB2 cells of cluster S4 (Bglap, Bglap2, Ptgis, Cd63, Il12a, Ank) (Supplementary Figure 8 and Figure 3C). These results confirm that the SIBLING protein network is indeed induced by CA-ERBB2 expression in SCs at the neonatal stage.
3.7. Induction of ERBB2 signaling in deafened adult mice results in up-regulation of Spp1 and Timp1, activation of CD44 receptor, and detection of ectopic cellular aggregates in the adult cochlear scala media
To determine if the SIBLING cluster could be induced at adult stages, we used immunostaining on sections of cochlea from adult young mice after a combination of damage-induced hearing loss and CA-ERBB2 induction. Male and female young adult mice with Control and CA-ERBB2 genotype were exposed to traumatic noise as described in the Methods (Figure 5A). At 3 days post noise exposure (3 DPN), the mice from both genotypes were randomly assigned to two groups, and treated with doxycycline (DOX) injection to initiate CA-ERBB2 expression; or with saline injection to use as reference. Mice were euthanized at 5 DPN, and their cochlea were dissected and processed for immunostaining with antibodies specific for SPP1, TIMP1, and the intracellular domain of the CD44 receptor.
FIGURE 5
Figure 5. SPP1 and TIMP1 together with CD44 signaling are up-regulated in cochlear cells 2 days after CA-ERBB2 induction in noise exposed young adults. (A) Timeline of noise exposure (NE), GFP activation (TAM), CA-ERBB2 activation (DOX), and hearing tests (HT) in young adult mice. Mice were exposed to 110 dB octave band noise for 2 h, and 3 days later injected with doxycycline (DOX) to induce CA-ERBB2 expression. HT were performed 1 DPN to confirm hearing loss. Immunostaining of cochlea sections revealed detection of SPP1 (B) and TIMP1 (C) together with activated CD44 receptor in CA-ERBB2 animals. Immunodetection for HCs (PVALB, red), and cells competent to express CA-ERBB2 (GFP, green), are shown in panels 1 and 2. Immunodetection of activated CD44 receptor (blue) is shown in panels 1 and 3. Immunodetection of SPP1 and TIMP1 are shown in panel 1, 3, and 4 (gray).
As shown in Figures 5B, C, SPP1 and TIMP1 were up-expressed in cochlear sections from CA-ERBB2 animals treated with DOX. The fluorescent immunoreactivity for SPP1 corresponded to GFP + cells, including cells near OHC that correspond to DC, and cells near IHC corresponding to phalangeal cells and border cells. Similarly, TIMP1 was detected in GFP + cells, although in sections from Control animals the immunoreactivity for TIMP1 was evident also in cells corresponding to inner phalangeal cells and border cells. Staining for the CD44 intracellular domain showed clearly up-regulation of CD44 signaling in GFP + cells from CA-ERBB2 animals treated with DOX. The CD44 immunoreactivity was also observed in interphalangeal cells, DC and also in cells corresponding to HeC or Claudius cells. Interestingly, CD44 activation in cells corresponding to HeC or Claudius cells was also evident in sections from Control animals. This is consistent with previous report describing CD44 expression to increase in postnatal mice by P7 in the OPCs, Claudius cells and in a small number of GER cells (Hertzano et al., 2010).
Additional mice exposed to traumatic noise, EdU, and doxycycline were euthanized at 7 DPN, and analyzed for GFP expression and additional markers (Figure 6). Here we found that aggregated GFP + and GFP-negative cells were located in the scala media of CA-ERBB2 cochlea. Phosphorylation of ERBB2 was seen in scattered cells, and did not precisely map onto GFP expression as observed at earlier time points (Zhang et al., 2018). Mitotic figures labeled with EdU were evident in these aggregates (Figure 6B’), as were scattered cells labeled with activated CASP3 (Figure 6C’). Scattered cells within aggregates expressed sensory markers, including MYO7 (Figure 6B’) and the SC marker TAK1 (Figure 6D’). They were largely absent of SOX2 (Figure 6A’) and PVALB (Figure 6D’) expression. Some aggregates had smooth, compacted multicellular regions that stained brightly for phalloidin. Aggregates were observed in four out of five cochleae with CA-ERBB2 induction. In 4 Control cochleae, only very small clusters of cells were observed floating in the cochlear duct, none of which expressed GFP or incorporated EdU (Figures 6E, E’, arrows). These data are consistent with the interpretation that activation of CA-ERBB2 signaling in young adult mice after damage can also induce the expression of some members of the SIBLING protein network. They also suggest that lineage-traced SCs may respond to expression of CA-ERBB2 by exiting the epithelium.
FIGURE 6
Figure 6. Four days after CA-ERBB2 induction, aggregates of sensory cells can be found within the cochlear duct. Top, shown timeline of noise exposure (NE), GFP activation (TAM), CA-ERBB2 activation (DOX), EdU injection, and hearing tests (HT) in young adult mice. Brightfield low power images are used to show the position of the cellular aggregates, while immunostaining reveals specific markers. (A, A’) GFP (green) and pERBB2 (magenta) are present in an aggregate attached to the spiral limbus, which has little SOX2 (white). (B, B’) A similarly localized aggregate harbors GFP + cells (green) and rare MYO7 + cells (white), with EdU + mitotic figures (magenta) in cells lacking GFP. (C, C’) An aggregate near the stria vascularis contains GFP + cells (green), rare apoptotic cells marked with anti-activated CASP3 (magenta), and compacted epithelial cells revealed by phalloidin staining (white). (D, D’) Another aggregate near the stria vascularis harbors cells with GFP (green) and neighboring cells positive for the supporting cell marker TAK1 (magenta), but no PVALB + HCs. (E, E’) A Control mouse lacking the CA-ERBB2 transgene harbors only small clusters of cells (yellow arrow) without GFP expression.
4. Discussion
Previously, we found that SCs with activated ERBB2 influenced gene expression in their neighbors in vivo and promoted the differentiation of hair-cell like cells, suggesting that ERBB2 may initiate a signaling cascade important for HC regeneration (Zhang et al., 2018). Here, single cell transcriptome analysis revealed the formation of new population among a subset of cells with activated ERBB2 signaling, which had differentiated significantly from the parental Control cells. Possibly derived from OPCs, these cells also express LGER-specific genes. They comprise most of the cells expressing Spp1, identified in our studies as one of the most highly activated genes in response to ERBB2 signaling. Importantly, in this novel population we see expression of the other three top up-regulated genes, Mmp9, Timp1, and Dmp1. Together with Spp1, they are associated with a signaling network involving CD44 and integrin αvβ3 receptors. GO enrichment analysis revealed that these genes modulate both the ECM and cytokine responses, including Notch signaling. We confirmed that SPP1, TIMP1, and CD44 protein are also up-regulated in adult cochlear SCs after CA-ERBB2 induction. Subsequently, we observed the formation of floating aggregates of cochlear sensory cells. The fate and potential of these cellular aggregates are not known.
SPP1 and DMP1 are secreted glycoproteins that act as ligands for CD44 and integrin αvβ3 receptors. They are members of the small integrin-binding ligand n-linked glycoprotein (SIBLING) family. SPP1 promotes survival, proliferation, differentiation, adhesion, and migration of numerous cell types (Flores et al., 1992; Ashkar et al., 2000; Sodek et al., 2000; Denhardt et al., 2001; Jain et al., 2002; Karadag et al., 2005; Rangaswami et al., 2006; Kazanecki et al., 2007). While DMP1 function in injury and wound healing has not been yet determined, it is significantly up-regulated in a number of cancerous tissues (Chaplet et al., 2003; Fisher et al., 2004). SPP1 may function in the neuronal differentiation of auditory neurons during inner ear development (Kim et al., 2014). Moreover, it is detected in membranous labyrinth of the adult mammalian cochleae, particularly in the utricle, where it is currently used as a marker of type I HC (Lopez et al., 1995; Sakagami, 2000; McInturff et al., 2018; Jan et al., 2021).
The most significant aspect of up-regulation of SPP1, MMP9, and TIMP1 in response to ERBB2 signaling, is that they promote wound healing and regeneration after injury in other systems (Denhardt et al., 2001; Kyriakides et al., 2009; Kim et al., 2012; Michopoulou et al., 2020). SPP1 is well known to mediate bone and muscle regeneration (Uaesoontrachoon et al., 2008; Zanotti et al., 2011; Pagel et al., 2014; Maeda et al., 2017; Zhu et al., 2020), and it is also involved in promoting proliferation and regeneration in nervous system (Ellison et al., 1998; Hedtjarn et al., 2004; Liu et al., 2017). In recent studies, Wang et al. demonstrated that binding of SPP1 with CD44 and integrin αvβ3 is important in the Schwann cells function in regenerating nerves, by promoting proliferation and survival after peripheral nerve injury (Wang et al., 2020). Another study by Powell et al. (2019) showed that SPP1 together with MMP9 acts through CD44 receptor to mediate synaptogenesis after central nervous system (CNS) insult.
TIMP1 is an inhibitor of MMP9 and the balance between them is a key regulator of the signaling network in the injured nerve (Kim et al., 2012) and promotes the healing process of burned fetal skin (Yu et al., 2017). The up-regulation of TIMP1 could explain the widespread downregulation of SOX2 after CA-ERBB2 signaling in vivo (Zhang et al., 2018), as MMP9 is necessary for NOTCH signaling (Zhao et al., 2016), and NOTCH is necessary and sufficient to promote SOX2 expression (Pan et al., 2013). An increased MMP9/TIMP1 ratio promotes the degradation of ECM to allow cellular migration, while a reduced MMP9/TIMP1 ratio drives reconstruction of the ECM during healing process (Yu et al., 2017). TIMP1 may also act as cytokine independently of MMP9 inhibition to promote cell survival and proliferation (Ries, 2014). In hematopoietic stem and progenitor cells, TIMP1 promotes migration, adhesion and survival by binding to CD63-integrin β1 receptors complex (Wilk et al., 2013). Our scRNA-seq analysis revealed CD63 as DEG and its up-regulation was mostly enriched in cluster S4 formed by CA-ERBB2 cells (Supplementary Tables 3, 4).
Up-regulation of SPP1, MMP9, TIMP1, and DMP1 in response to ERBB2 activation suggests that its downstream signaling involves CD44 receptor and potentially also integrin receptors. The relationship between ERBB2 and CD44 was previously described for maintaining neuron–Schwann cell interactions in early rat neonatal nerves development (Sherman et al., 2000). In particular, CD44 significantly enhanced neuregulin-induced ERBB2 phosphorylation and ERBB2–ERBB3 heterodimerization. CD44 was also found to interact with ERBB2 receptor (Bourguignon et al., 1997; Sherman et al., 2000). Importance of CD44 receptor’s network in cells survival, proliferation and regeneration described for Schwann cell and in other tissues, suggests that some of CA-ERBB2 effects involve signaling through CD44 receptor.
Lower flexibility of the epithelium associated with cell-cell junction was proposed as one of the mechanisms responsible for decreased regenerative capacity of the adult mammalian cochlea (Burns et al., 2008). Our results indicate that ERBB2 signaling promotes modulation of ECM that would allow increased flexibility in the organ of Corti. The combination of EGF and GSK3 inhibitors were recently reported to deplete E-cadherin in tight junctions of the adult mammalian cochlea (Kozlowski et al., 2020). In addition to up-regulated genes associated with ECM disassembly in cluster S4, there is also up-regulated Plet1 gene in CA-ERBB2 cells from cluster S7, which is associated with negative regulation of cell-matrix adhesion (GO:0001953). Plet1 is listed in GO terms associated with spreading of cells and wound healing (GO:0035313, GO:0044319). Thus, we would predict that its up-regulation would allow for increased local movements of cells.
Importance of ERBB2-mediated ECM modulation for HCs regeneration is also supported by recent studies indicating that ECM and integrin receptors are induced in early neurosensory development and cell fate determination in the human fetal inner ear (Johnson Chacko et al., 2021). We speculate that enforced activation of signaling pathways through ERBB family receptors might allow for changes in the environment of the organ of Corti that promote the proliferation of SCs and permit the regeneration of HCs. Previous studies have shown little or no stem cell activity in the adult mammalian cochlea (Oshima et al., 2007; Senn et al., 2020). This contrasts to robust stem-like capacity in isolated cells from the adult utricle (Li et al., 2003; Senn et al., 2020), which correlates with limited regeneration potential in that organ (Burns and Stone, 2017). These data may be interpreted to mean that cochlear stem cells, perhaps resident in GER (Udagawa et al., 2021), are lost during maturation. It is also possible that their requirements for survival or for identity maintenance differ. For example, they may require accessory cells to maintain their microenvironmental niche. Alternatively, the forced expression of CA-ERBB2 signaling might promote novel behaviors not otherwise seen in cochlear SCs.
In conclusion, we report that enforced signaling of ERBB2 in a minority of cochlear SCs drives a novel differentiation response in the neonatal mouse cochlea. These cells induce expression of a cluster of genes involved in signaling, wound healing, and migration. We confirm that at least two of these genes, SPP1 and CD44, are also up-regulated in adult cochlear cells after CA-ERBB2 induction. CA-ERBB2 induction also correlates with the generation of cellular aggregates in the cochlear duct. These aggregates contain, but are not limited to, fate-mapped CA-ERBB2 cells. Their potential, effects, and fate remain to be determined.
Data availability statement
The data presented in this study are deposited in the Gene Expression Omnibus data repository, accession number: GSE202850 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE202850). The image data available from: https://osf.io/r9cbq/.
Ethics statement
This animal study was reviewed and approved by the Animal Care and Use Review Office, Department of Defense, and the University Committee on Animal Research, University of Rochester.
Author contributions
DP-P: project administration, investigation, methodology, data curation, formal analysis, visualization, writing – original draft and review, and editing. DN and CB: data curation, formal analysis, software, visualization, and writing – review and editing. JZ: methodology, investigation, visualization, and writing – review and editing. JA: conceptualization, supervision, resources, and writing – review and editing. PW: conceptualization, funding acquisition, resources, supervision, formal analysis, and writing – review and editing. All authors contributed to the article and approved the submitted version.
Funding
This work was funded by the U.S. Army Medical Research Mechanism W81XWH2010515 grant number RH190035, and the NIDCD grant R01 DC014261.
Acknowledgments
We gratefully acknowledge Dr. Anne Luebke, who maintains the URMC Small Animal Auditory Testing Core; Dr. Jian Zuo for the Fgfr3-iCre mouse strain; Dr. Lin Gan for the ROSA-floxed rtTA/GFP mouse strain; and Dr. Amy Kiernan for advice on experimental interpretation and for critically reading the manuscript.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fncel.2022.1096872/full#supplementary-material
Footnotes
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Keywords: cochlear regeneration, candidate pathway, ERBB2, single cell sequencing, SIBLING, CD44
Citation: Piekna-Przybylska D, Na D, Zhang J, Baker C, Ashton JM and White PM (2023) Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor indicates a cell-specific response that promotes CD44 activation. Front. Cell. Neurosci. 16:1096872. doi: 10.3389/fncel.2022.1096872
Received: 12 November 2022; Accepted: 12 December 2022;
Published: 06 January 2023.
Edited by:
Chen Chen, Stanford University, United StatesReviewed by:
Ping-Chung Chen, St. Jude Children’s Research Hospital, United StatesRobert J. Morell, National Institute on Deafness and Other Communication Disorders (NIH), United States
Copyright © 2023 Piekna-Przybylska, Na, Zhang, Baker, Ashton and White. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Patricia M. White, 
patricia_white@urmc.rochester.edu
†Present Address: Jingyuan Zhang, Department of Otolaryngology, Boston Children’s Hospital, Boston, MA, United States