Long Non-coding RNAs and mRNAs Expression Profiles of Monocyte-Derived Dendritic Cells From PBMCs in AR

Objective: The objective of this study is to explore the long non-coding RNAs (lncRNAs) and messenger RNAs (mRNAs) expression profiles of monocyte-derived dendritic cells (DCs) obtained from peripheral blood mononuclear cells (PBMCs). DCs are known to play a major role in the regulating function of allergic rhinitis (AR).

Methods: PBMCs were separately isolated from the human peripheral blood of patients with AR and normal person (NP). The mixed lymphocyte reaction (MLR) assay was used to evaluate the function of DCs. Flow cytometry was used to determine the immune regulatory function of immature DCs (imDCs) and mature DCs (mDCs). lncRNAs and mRNAs in the NP group (DCs isolated from NP) and the test group (DCs isolated from patients with AR) were identified via chip technology and bioinformatic analyses. Moreover, bioinformatic analyses were employed to identify the related biological functions of monocyte-derived DCs and construct the functional networks of lncRNAs and mRNAs that are differentially expressed (DE) in imDCs and mDCs.

Results: MLR was significantly higher in the mDCs group than that in the imDCs group. CD14 was highly expressed in imDCs, whereas HLA-DR, CD80, and CD86 were highly expressed in mDCs (p < 0.001). We identified 962 DE lncRNAs and 308 DE mRNAs in the imDCs of NP and patients with AR. Additionally, there were 601 DE lncRNAs and 168 DE mRNAs in the mDCs in the NP and test groups. Quantitative RT-qPCR was used to study the significant fold changes of lncRNAs and mRNAs. The Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis found 16 significant regulated pathways in imDCs and 10 significant regulated pathways in mDCs, including the phagosome, cell adhesion signaling pathway, and inflammatory mediator regulation of TRP channels pathway.

Conclusion: Our research studied the lncRNA and mRNA expression profiles of monocyte-derived DCs and demonstrated the functional networks that are involved in monocyte-derived DCs-mediated regulation in AR. These results provided possible molecular mechanisms of monocyte-derived DCs in the immunoregulating function and laid the foundation for the molecular therapeutic targets of AR.

Background

Allergic rhinitis (AR) is a very common allergic disease that affects 10–40% of the global population (Bousquet et al., 2008). Its remarkable prevalence and relapses put an extensive burden on its patients and the society. Furthermore, AR negatively impacts the quality of life of patients with AR. There had been a marked increase in the prevalence of AR during the past years (Wang et al., 2016). AR turns into asthma if it is not treated in time, and the adequate treatment of AR can alleviate the severity of asthma (Leynaert et al., 2004). Researchers have illustrated that mast cell infiltration, lymphocytes imbalance, and goblet cell hyperplasia are involved in the pathogenesis of AR (Ouyang et al., 2010; Poggi et al., 2012). AR, which is a type I allergic disorder that is mediated by IgE humoral immune response, is accompanied by an influx of eosinophils and T helper 2 cells that secrete pro-inflammatory cytokines, namely, IL-4, IL-5, and IL-13 (Wilson et al., 2005). Abnormal innate and adaptive immune responses play a major role in the pathogenesis of AR.

Dendritic cells (DCs), which are the most important antigen-presenting cells (APCs) that send signals to the T cells, mainly participate in the pathogenesis of many diseases with immunoregulatory mechanisms, such as AR. DCs link the innate and adaptive immune responses. The peripheral blood mononuclear cells (PBMCs) have a round nucleus (Delves, 2016). PBMCs include lymphocytes, monocytes, and DCs. In humans, the frequencies of these DCs vary among individuals. PBMCs are divided into various functional subtypes with respect to the specific cytokine expression profiles, surface markers, and the transcription factors. Phenotypic and functional assessments of PBMC research lay the foundation of the human immune system research; hence, the knowledge that population is represented in the peripheral blood and how they act with other immune cells is essential. Additionally, the results from human PBMC studies (Schiekofer et al., 2003; Tacconi et al., 2004; Chang et al., 2014) cannot be neglected. Therefore, it is important to know the progression of AR along with its expression profiles in PBMCs, especially DCs.

Long non-coding RNAs (lncRNAs), over 200 nt in length, is a type of RNA that does not a protein coding function (Ulitsky and Bartel, 2013). These RNAs have been regarded as indispensable epigenetic regulators and are probably involved in the cell’s biological behaviors (Kopp and Mendell, 2018). For example, they are involved in regulating the homeostasis of the immune system (Wang et al., 2014; Du et al., 2017). However, it is critical to find out whether lncRNA can immunoregulate DC in the progression of AR.

The combination of lncRNA–messenger RNA (mRNA) expression profiles and functional networks is adopted to analyze the DC-mediated regulation functions. These results improve our understanding of lncRNAs in the immunoregulatory function of monocyte-derived DCs and indicate the potential targets for the curative treatment of AR.

Materials and Methods

Subjects

Patients with AR visited doctors in the outpatient service in the Guo Yi Tang of Beijing University of Chinese Medicine. In this study, there were 24 subjects: 12 males and 12 females. They were divided into two groups: the AR group (patients with AR, 12 subjects: five males and seven females) and NP group (normal persons, 12 subjects: four males and eight females). With support/approval from the Ethics Committee of Beijing University of Chinese Medicine, this study was conducted while adhering to the principles of the Declaration of Helsinki. Patients in the AR group were positive for skin puncture test, including pollen, food, dust mites, paint, or molds as well as in specific IgE. Two weeks before study recruitment, these patients with AR received no topical or systemic corticosteroid therapy. We chose the study participants with no history of smoking or other immune system disorders, such as rheumatoid arthritis, systemic lupus erythematosus, and scleroderma.

Isolation of PBMCs and Generation of DCs

The whole blood samples obtained from the two groups were stored in vacuum tubes with heparin, and PBMCs were isolated from these samples by lymphocyte separation solution (Tianjin Haoyang Biological Manufacture Co., Ltd.). Mononuclear cells were seeded in 12-well plates with the RPMI 1640 medium that contains 10% heat-inactivated fetal calf serum (FCS, GIBCO, Germany) and 2 mM of L-glutamine (R10 medium, Sigma, St. Louis, MO, United States). After incubation at 37°C for 2 h, the non-adherent cells were removed and the adherent cells were cultured within the medium containing 100 ng/ml of rhGM-CSF and 100 ng/ml of rhIL-4 (R&D Systems, Minneapolis, MN, United States). On the sixth day, 50 ng/ml of TNF-α (R&D Systems, Minneapolis, MN, United States) was added into the samples; the method had the same protocol in the study of Andreia et al. (2005). Immature DCs (imDCs) were collected on the fifth day, and the mature DCs (mDCs) were collected on the seventh day.

Mixed Lymphocyte Reaction (MLR)

After being treated with 25 μg/mL of mitomycin at 37°C for 30 min, the DCs were placed at the concentrations of 2 × 10⁸ cells per well at a quantity of 200 μl and incubated with non-adherent PBMCs obtained from the same healthy people. These samples were later stimulated by lymphocytes in the concentration proportions of 1:10, 1:50, and 1:100. Thereafter, the samples were mixed and incubated with non-adherent PBMC from the same healthy persons at the same concentrations in triplicate. The cells were treated with 10% fetal bovine serum. Then, 10 μl of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) solution (5 mg/ml, medium dilution, Sigma–Aldrich Chemical Co., St. Louis, MO, United States) was added to each well, and the cells were incubated for 72 h in the incubator. Then, 150 μl of DMSO was added followed by the addition of enzymes after 4 h. The absorbance was detected using a spectrophotometer at 570 nm.

DC Surface Marker Expression Analysis in imDCs and mDCs

The CD14 (PerCP-Cy 5.5, BD Biosciences, United States), HLA-DR (APC, BD Biosciences, United States), and isotype mouse IgG2a-PE (PE, BioLegend, United States) were added in the samples of imDCs. Moreover, CD86-APC, CD80-PE, and isotype mouse IgG1–FITC (BioLegend, United States) were added in the samples of mDCs. The cells were then suspended with precooled PBS, counted under a microscope, and centrifuged at 1000 g for 5 min. Data were acquired using a FACSCalibur cytometer (BD Biosciences, United States) and the ratios of CD14⁺, HLA-DR⁺, CD80⁺, and CD86⁺ DCs were determined.

RNA Extraction, Labeling, Chip Hybridization, and Scanning

The RNA extraction, labeling, chip hybridization, and scanning were all finished following the use of Agilent Human lncRNA–mRNA profiling chip (4^∗180K, Design ID: 062918). All the chip results were detailed according to the processes of software operations. The screening criteria were to increase or decrease the fold change value ≥ 2.0 and p-value < 0.05.

Gene Ontology (GO) and Pathway Enrichment Analysis

The GO and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis were used to study the differentially expressed (DE) mRNAs. The results of the target gene analysis of lncRNA and the mRNA expression results on the chip need to be correlated so that the upregulated and downregulated DE genes can be investigated. The corrected p-value < 0.05 by calculating the FDR and FDR < 0.05 was selected as the threshold.

LncRNA–mRNA-Weighted Co-expression Network

The correlation of the lncRNA–mRNA expression in the imDCs and mDCs was calculated. Then, the relationship pairs of LncRNA and mRNA based on the abovementioned criteria (p-value < 0.05, FDR < 0.05) were screened. The co-expression network of lncRNAs and mRNAs was constructed, and the co-expression network of lncRNAs and mRNAs was then established.

Real-Time PCR Verification of DE Genes

Quantitative RT-qPCR was used to investigate the different expressions of imDCs’ and mDCs’ genes between the patients with AR and NP. The total RNA was extracted from imDCs and DCs according to the kit for cells. In all, 20 μg of total RNA was converted into cDNA by using oligo (dT) and reverse transcriptase (Thermo, United States) to analyze the qPCR results. The thermal cycler conditions were set as follows: amplificated at 95°C for 10 min, 95°C for 15 s, 60°C for 60 s, 40 cycles of denaturation (15 s, 94°C), 15 s at 95°C, and a combined process of annealing and extension (1 min, 60°C). Supplementary Table S1 shows the primers for these genes.

Statistical Analysis

The SPSS 22.0 software was used for statistical analysis in this study. Results were expressed as mean ± standard deviation. The relationship of lncRNAs and mRNAs was determined by the Spearman’s correlation coefficient. p-values < 0.05 were considered significant values for this study.

Results

Allogeneic T-Cell Proliferation Experiment

In allergenic mixed lymphocyte reaction (MLR), the levels of T-cell proliferation were increased with the proportion of T cells. DCs in the patients with AR have a stronger stimulation ability than NP as shown in Figures 1A–C. When the ratio of DC cells to T cells was 1:50 and 1:100, the difference was significant (p < 0.001).

FIGURE 1

Figure 1. Morphology of dendritic cells and the functional activity of DCs were assayed by autologous MLR. (A,B) imDCs and mDCs, mDCs have a more structure of dendrites. (C) MLR was determined by the stimulation index. 2 × 10⁸ ml^–1 DCs and lymphocytes were cultured with the medium for 72 h, and then DCs were collected and autologous MLR was performed. The control group was stimulated with 25 mg/L mitomycin as controls. ***P < 0.001.

Immunophenotype of DCs in Patients With AR and NP

We evaluated the percentages of CD14, HLA-DR, CD80, and CD86 in the DCs. The immunophenotypic characteristics of DCs in patients with AR were compared with that of NP, as shown in Figure 2. The CD14 concentration of imDCs was lower in patients with AR than that in the NP group. The mean percentage of CD14⁺ DCs in the patients with AR was 0.84 ± 0.25% (median: 0.78%), and it was significantly lower than the value in the NP group (p = 0.0008), where the mean percentage of these cells was 0.012 ± 0.013% (median: 0.017%) (Figures 2A,B).

FIGURE 2

Figure 2. Flow cytometric analysis showing the percentage of CD14, HLA-DR, CD80, and CD86 in DCs. (A,B) The flow cytometric analysis showed that percentage of CD14 in NP group was lower than that in AR group (p = 0.0008). (C,D) The flow cytometric analysis showed that percentage of HLA-DR in NP group was lower than that in AR group. (E,F) The flow cytometric analysis showed that percentage of CD80 in NP group was lower than that in AR group. (G,H) The flow cytometric analysis showed that percentage of CD86 in NP group was lower than that in AR group. ***P < 0.001, **P < 0.01.

The mean proportion of HLA-DR⁺ mDCs in the patients with AR was 44.25 ± 8.64% (median: 44.8%) and was higher (p = 0.0006) than the NP group, where the mean percentage of these cells was 95.3 ± 3.84% (median: 99.0%) (Figures 2C,D).

The mean proportion of CD80⁺ mDCs in the patients with AR was 72.15 ± 7.64% (median: 67.78%) and was higher (p = 0.0003) than the NP group, where the mean percentage of these cells was 95.3 ± 3.84% (median: 96.92%) (Figures 2E,F).

The mean proportion of CD86⁺ mDCs in the patients with AR was 62.15 ± 7.64% (median: 64.69%) and was higher (p = 0.006) than the control group, where the mean percentage of these cells was 92.3 ± 5.84% (median: 95.12%) (Figures 2G,H).

Identification of DE lncRNAs and mRNAs in imDCs

In total, 308 DE mRNAs, including 175 upregulated mRNAs and 133 downregulated mRNAs, were found in the imDCs of patients with AR and NP. A clustergram (Figure 3A) and volcano plots (Figure 3C) are used to depict DE mRNAs. Table 1 shows 67 mRNAs with the largest fold changes. The list contains several genes, including HLA-C, MARCO, KIR2DS3, ITGAV, CD36, and IFNB1. Additionally, 168 DE mRNAs, including 77 upregulated mRNAs and 91 downregulated mRNAs, were found in the mDCs of patients with AR. Figures 4A,C show the clustergram and volcano plots of the DE mRNAs, respectively. Table 2 shows the 10 mRNAs with the greatest variation, and several genes, such as HLA-B, F11R, HLA-DQB1b, HLA-DQB1, and PTAFR, are also shown.

FIGURE 3

Figure 3. Identification of DE lncRNAs and mRNAs, GO, and KEGG analysis in imDCs. (A) Heatmaps of DE mRNAs between the AR group and NP group. (B) Heatmaps of DE lncRNAs between the AR group and NP group. (C) Volcano plots of DE mRNAs between the AR group and NP group. (D) Volcano plots of DE lncRNAs between the AR group and NP group. (E) Top 10 terms from a GO analysis of molecular function, biological process, and cellular component. (F) DE mRNAs were clustered by KEGG analysis, and the top 10 pathways are shown.

TABLE 1

Table 1. The characteristics of mRNAs with the largest fold change in imDCs.

FIGURE 4

Figure 4. Identification of DE lncRNAs and mRNAs, GO, and KEGG analysis in mDCs. (A) Heatmaps of DE mRNAs between the AR group and NP group. (B) Heatmaps of DE lncRNAs between the AR group and NP group. (C) Volcano plots of DE mRNAs between the AR group and NP group. (D) Volcano plots of DE lncRNAs between the AR group and NP group. (E) Top 10 terms from a GO analysis of molecular function, biological process, and cellular component. (F) DE mRNAs were clustered by KEGG analysis, and the top 10 pathways are shown.

TABLE 2

Table 2. The top 10 co-expression of mRNA and lncRNA in imDCs.

In total, 962 DE lncRNAs, including 434 upregulated and 528 downregulated lncRNAs, were found in patients with AR and NP. The clustergram (Figure 3B) and volcano plots (Figure 3D) show DE lncRNAs. In total, 601 lncRNAs, including 200 upregulated and 401 downregulated lncRNAs, were found in the DE mDCs of the patients with AR. The clustergram in Figure 4B and the volcano plots in Figure 4D show the DE lncRNAs. Tables 1, 3 show the top 10 lncRNAs of imDCs and mDCs with the largest fold changes. The pathways, including interferon-gamma-mediated signaling pathway, membrane repolarization, and peptide antigen binding, that contribute to the phagocytosis function in imDCs and antigen-presenting function of mDCs were also identified.

TABLE 3

Table 3. The characteristics of mRNAs with the largest fold change in mDCs.

Interaction, Co-expression Network Analysis of DE mRNAs in Patients With AR

Figure 5A shows the interactions of proteins that were coded by DE mRNAs in imDCs. Additionally, Figure 5B shows the co-expression network between DE lncRNAs and mRNAs. TRIM69 has the maximum target mRNAs including 58 DE mRNAs, and SIDT2 has the maximum co-expressed lncRNAs. Table 2 shows the top 10 co-expression pairs in imDCs. lncRNAs exert their biological function as ceRNAs (Wilfried et al., 2016).

FIGURE 5

Figure 5. Interaction and co-expression network analysis, analysis of lncRNA target mRNAs in imDCs. (A) Interactions between DE mRNAs. Purple indicates upregulated genes, and green indicates downregulated genes. (B) Co-expression network of DE lncRNAs and DE mRNAs. (C) DE lncRNAs and their target genes with a combined score larger than 0.9 are shown. Yellow indicates upregulated genes, and blue indicates downregulated genes. (D) Venn diagram showing DE mRNAs and target genes of DE lncRNAs.

We identified 268 target genes after analyzing the possible DE lncRNAs target genes in imDCs. Figure 5C shows the target genes with a combined score of more than 0.9. HLA-C was the target gene of AC108142.1-005, and CD36 was the target gene of FR264384. Moreover, IFNB1 was the target gene of MIR3150B-210. The Venn diagram analysis showed that 95 mRNAs were coincided between the 166 DE mRNAs and the 95 DE lncRNA target genes (Figure 5D). The 95 DE lncRNAs were all included in the 166 DE mRNAs.

Figure 6A shows the interaction proteins that were coded by DE mRNAs in mDCs. In this network, HLA-B, HLA-DQB1, HLA-DQB2, PTAFR, and F11R are important genes that interact with many other DE mRNAs. Furthermore, Figure 6B shows the co-expression network of DE lncRNAs and mRNAs. TRIM77P has the maximum target numbers including 39 DE mRNAs, in which FAM153A and ZNF396 have the maximum co-expressed lncRNAs. Table 4 shows the top 10 co-expression pairs of mDCs.

FIGURE 6

Figure 6. Interaction and co-expression network analysis, analysis of lncRNA target mRNAsin mDCs. (A) Interactions between DE mRNAs. Purple indicates upregulated genes, and green indicates downregulated genes. (B) Co-expression network of DE lncRNAs and DE mRNAs. (C) DE lncRNAs and their target genes with a combined score larger than 0.9 are shown. Yellow indicates upregulated genes, and blue indicates downregulated genes. (D) Venn diagram showing DE mRNAs and target genes of DE lncRNAs.

TABLE 4

Table 4. The top 10 co-expression of mRNA and lncRNA in mDCs.

Additionally, we also investigated the possible presence of DE lncRNA target genes in mDCs. In our study, 99 target genes were identified in these DE lncRNAs. Figure 6C shows the target genes with the combined score of more than 0.9. In the figure, HLA-B has three target genes of lincRNAs, namely, DHRS3, FCHO2, and linc-PRR5-1. Figure 6D shows that 42 mRNAs coincided between the 95 DE mRNAs and the 42 DE lncRNA target genes in the Venn diagram analysis. Moreover, the 42 DE lncRNAs were included in the 95 DE mRNAs. It also includes some known inflammatory-related molecules.

Validation of DE mRNA and lncRNA Expression Levels by RT-qPCR

RT-qPCR was used to evaluate DE mRNAs and lncRNAs to verify our RNA chip results. We randomly detected three lncRNAs and 10 mRNAs. MARCO, KIR2DS3, F11R, HLA-B, HLA-C, NON-HSAG046717, and NON-HSAT089067 were upregulated, whereas ITGAV, CD36, IFNB1, PTAFR, HLA-DQB1, NON-HSAT 059748, NON-HSAT024276, and NON-HSAT098958 were downregulated. The results of RT-qPCR were consistent with those of RNA chip results, hence confirming that our chip data were reliable (Figure 7).

FIGURE 7

Figure 7. Validation of DE mRNAs and lncRNAs. (A,B) DE mRNAs were confirmed by qPCR. (C) DE lncRNAs were confirmed by qPCR. Ligand 1, MACO, the scavenger receptor; Ligand 2, KIR2DS3, a type of killer cell immunoglobulin-like receptors (KIRs); Ligand 3, F11R, a cell adhesion molecule found on the surface of human platelets; Ligand 4 and Ligand 5, HLA-B and HLA-C are all a type of human Leukocyte Antigen (HLA) class I molecules; Ligand 6, ITGAV, integrin subunit alpha v; Ligand 7, CD36, a membrane glycoprotein present on platelets, mononuclear phagocytes, adipocytes, hepatocytes, myocytes, and some epithelia; Ligand 8, IFNB1, interferon beta, a secreted cytokine; Ligand 9, PTAFR, platelet-activating factor receptor; Ligand 10, HLA-DQB1, human leukocyte antigen DQB1. **P < 0.01, *P < 0.05.

Discussion

In our research, we used rhGM-CSF, rhIL-4, and TNF-α to induce the mDCs from PBMCs. The generation of human monocyte-derived DCs from whole blood was recognized by all the scientists (Wilfried et al., 2016). We investigated phenotypic and functional features of DE DCs in vitro from patients with AR and the NPs. Besides that, we used RT-qPCR to confirm these findings. Our KEGG pathway analysis (Tables 5, 6) indicates that interferon-gamma-mediated signaling pathway, membrane repolarization, and peptide antigen binding pathways contribute to the phagocytosis function in imDCs, and the antigen-presenting function in mDCs contributes to the immunoregulatory function of DCs in AR.

TABLE 5

Table 5. Pathways KEGG analysis of imDCs.

TABLE 6

Table 6. Pathways of mDCs with the largest significant difference in KEGG analysis.

Dendritic cells play a central role in allergic inflammation (Froidure et al., 2016). The latest in vitro techniques allow the in vitro differentiation of DCs (Thurner et al., 1999). Their ability to induce the proliferation of T cells in the MLR assay is commonly used for evaluating their functions (Cao et al., 2004). In MLR experiment, the stimulation index of mDCs was significantly higher than that of the imDCs. In our study, the expression of HLA-DR, CD80, and CD86 in patients with AR is indeed upregulated than that in NP, which is a sign of improved mDCs antigen presentation in patients with AR. This result is in accordance with a previous study by KleinJan et al. (2006). In the study, CD14 in the NP group was higher than that in patients with AR. CD14 is the marker of monocytes whose expression decreases gradually during DC differentiation from monocytes. In fact, CD80 and CD86 are important co-stimulating factors that affect the proliferation of T lymphocytes in the DCs (Duperrier et al., 2000; Ebner et al., 2001; Andreia et al., 2005; Wilfried et al., 2016). DCs are the most efficient APCs. It can present the antigens to the T cells for stimulating the adaptive immune response.

More number of studies have focused on exploring the mRNA expressed in DCs, but none have been conducted to reveal which and how mRNA affects DCs in patients with AR. To investigate the mechanism of DCs’ functions in patients with AR, the mRNA expression profile was determined and bioinformatics analysis was performed in our study. In total, 308 mRNAs were identified in the analysis. Among these DE genes, HLA-C, ITGAV, MARCO, CD36, IFNB1, and KIR2DS3 were found to be most significantly upregulated in the imDCs’ network. HLA-C plays an important role in promoting differential DC maturation (Raj et al., 2011). ITGAV is the expression of DC-specific transmembrane protein. MARCO promotes TLR activation, which validates a major role of MARCO in mounting an inflammatory response (Haydn et al., 2014). ImDCs play an important role in the phagocytosis of apoptotic cells, in particular, CD36 (Albert et al., 1998). Additionally, the GO analysis demonstrated specific molecular functions, for example, binding of transforming growth factor-beta, signaling pattern recognition receptor activity, and pattern recognition receptor activity, thereby indicating the critical role of these cytokines in the immunoregulatory functions of imDCs. The KEGG analysis identified 17 signaling pathways of the DE mRNAs, wherein interferon-gamma-mediated signaling pathway, membrane repolarization, and peptide antigen binding were the pathways with the significant differences that contributed to the phagocytosis function of imDCs (Figures 3E,F). This result is consistent with that of a previous study (Lambrecht, 2001). Although research works have been conducted to determine the functions of imDCs in AR, the role of IFNB1 and KIR2DS3 in imDCs was not known in AR (Tables 7, 8).

TABLE 7

Table 7. GO analysis of DE mRNA in imDCs.

TABLE 8

Table 8. GO analysis of DE mRNA in mDCs.

The imDCs migrate to the lymphoid organs that will be matured in the future. They present captured Ag to the naïve T cells (Banchereau and Steinman, 1998). Hence, the imDCs and mDCs had different functions in the presented Ag. In our study, we focused on the immature and mature stages of DCs. In the mDC’ mRNA analysis, 168 mRNAs were identified. Among these DE genes, HLA-B, HLA-DQB1, HLA-DQB2, PTAFR, and F11R were the most significantly upregulated genes in mDCs. HLA-B is the major histocompatibility complex (class I) antigens that present the processed antigens. HLA-DQB1 is the major histocompatibility complex (class II) antigens that have been identified as useful biomarkers of candidacy for effective allergy immunotherapy in patients with AR (Yanming et al., 2019). This result indicates that these cytokines affect the antigen-presenting process in the mDCs. We can determine from the KEGG analysis that there are 12 signaling pathways related to DE mRNAs. The cell adhesion molecules were the useful pathways that contribute to the antigen-presenting function in mDCs (Figures 4E,F), which is consistent with a previous study (Roche and Furuta, 2015). Although many genes have been identified to play an important role in mDCs, but the mechanisms by which HLA-DQB2, PTAFR, and F11R affect mDC in AR are unknown (Tables 9, 10).

TABLE 9

Table 9. lncRNAs in imDCs with the largest fold change.

TABLE 10

Table 10. The characteristics of lncRNAs with the largest fold change in mDCs.

Long non-coding RNA is an important component in the mRNA expression profiles (Kopp and Mendell, 2018). Several studies have shown that the differentiation of DCs is closely related to lncRNAs (Pin et al., 2014; Majid et al., 2020). It is confirmed from our studies that lncRNA may play a key role in the development of DC. Our data showed that 172 lncRNAs of imDCs and 104 lncRNAs of mDCs were significantly expressed in patients with AR as compared to that in NP by at least twofold changes. This result helps in studying the AR-related global transcriptome.

Long non-coding RNAs do not have a protein coding function, but they can be used as a new modulator, such as cis- or trans-gene regulating expression, demethylation-promoting effect, and mRNA-processing control were the major mechanisms (Sone et al., 2007; Wahlestedt, 2013; Qiao et al., 2016). To analyze the functions of lncRNAs, mRNA–lncRNA was used to create a co-expression profile to predict the potential functions of the DE lncRNAs of patients with AR. We found that the DE lncRNAs were all included in the results of mRNA–lncRNA chip results.

We used RT-qPCR to validate the mRNA–lncRNA chip results with only one randomly selected transcript, and found that the RT-qPCR results are consistent with the chip results in better understanding the role of lncRNA in the pathogenesis of DC-mediated AR.

In summary, our study proved that several mRNAs and lncRNAs of DC affect a certain process of AR pathogenesis by regulating the target genes. This result points out the direction for future studies on determining and explaining the functions and mechanisms of AR-related mRNA and lncRNA, and provides new therapeutic targets for patients with AR.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by the medical and experimental animal ethics committee of Beijing University of Traditional Chinese Medicine. The patients/participants provided their written informed consent to participate in this study.

Author Contributions

YZ, XC, and YZ carried out the experiments. JW, QW, YZ, XC, and YZ designed the study and edited the manuscript. All authors read and approved the final manuscript.

Funding

This work was supported by grants from the National Natural Science Foundation of China (No. 81973715) and Beijing Natural Science Foundation of China (No. 7202110).

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.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcell.2021.636477/full#supplementary-material

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