Liang He
Furong Zhang1- 1Department of Anesthesiology, Yan'an Hospital of Kunming City, Kunming Medical University, Kunming, China
- 2Department of Anesthesiology, The First Affiliated Hospital of Kunming Medical University, Kunming, China
Patients with Alzheimer's disease (AD), Parkinson's disease (PD), traumatic brain injury (TBI), stroke, and postoperative neurocognitive disorder (POND) are commonly faced with neurocognitive disorders with limited therapeutic options. Some non-coding ribonucleic acids (ncRNAs) are involved in the development of various brain cognitive disorders. Circular RNAs (circRNAs), a typical group of ncRNAs, can function as competitive endogenous RNAs (ceRNAs) to dysregulate shared microRNAs (miRNAs) at post-transcription level, inhibiting regulation of miRNAs on their targeted messenger RNAs (mRNAs). circRNAs are abundant in central nervous system (CNS) diseases and cause brain disorders, but the exact roles of circRNAs are unclear. The crosstalk between circRNA, miRNA, and mRNA plays an important role in the pathogenesis of these neurocognitive dysfunction diseases and abnormal conditions including AD, PD, stroke, TBI, and POND. In this review, we summarized the participation of circRNA in neuroglial damage and inflammation. Finally, we aimed to highlight the regulatory mechanisms of circRNA–miRNA–mRNA networks in the development of various brain cognitive disorders and provide new insights into the therapeutics of these diseases.
Introduction
Microribonucleic acids (miRNAs) are small, non-coding, single-stranded linear RNAs spanning an average of 22 nucleotides in length. miRNAs can bind to the 3′ untranslated region (UTR) of messenger RNAs (mRNAs) via miRNA recognition elements (MRE) of target genes, which are presented in repression or degradation at the posttranscriptional levels, resulting in the dysregulation of the expression of target proteins (Salmena et al., 2011; Salim et al., 2022). Unlike classical linear RNAs, circular RNAs (circRNAs) are a novel group of evolutionarily conserved non-coding RNAs (ncRNAs) that form covalently closed continuous loop structures without 5' caps or 3' Poly A tails and act as sponges of miRNAs (Kristensen et al., 2019; Chen et al., 2022). Here, a total of 262,782 circRNAs have been presented in CIRCpedia v2 embracing over 180 RNA-seq data sets that cross six different species (Dong et al., 2018). Meanwhile, the crosstalk mechanism between circRNA, miRNA, and mRNA is not clearly understood.
As mentioned above, most genomes are presented in a miRNA-dependent repression manner and are densely covered in MREs like the letters of an “RNA language,” which function as the entire mRNA dimension by identifying competitive endogenous miRNA (ceRNA) networks in the ncRNA pool (Salmena et al., 2011; Hansen et al., 2013). The ceRNA of long ncRNA in miRNA regulation is validated (Salmena et al., 2011). Some circRNAs could function as molecular sponges for other RNA transcripts through their miRNA binding sites by ceRNA (Hansen et al., 2013). circRNA functions as miRNA sponge to dysregulate stability, transcription, and translation of mRNAs (Figure 1), which are the target genes of miRNAs, in complicated mechanisms (Hansen et al., 2013; Yesharim et al., 2021; D'Anca et al., 2022).
Figure 1. Circular RNAs (CircRNAs) act as the sponges of microRNAs (miRNAs) in neuroglial damage. Main circRNAs can act as miRNA sponges, resulting in the inhibition of miRNA on its target genes and/or proteins, and function as important roles in neuronal damage. Some circRNAs derived from extracellular vesicles (EVs) in astrocytes are beneficial for the attenuation of neurological disorders.
A lot of studies indicate that the crosstalk between circRNAs, miRNAs, and mRNA can participate in many pathophysiological processes in the development of cerebral diseases (or abnormal conditions), such as Alzheimer's disease (AD) (Lu et al., 2019; Li et al., 2022), Parkinson's disease (PD) (Wang et al., 2021; Liu et al., 2022), traumatic brain injury (TBI) (Huang X. J. et al., 2022; Zheng et al., 2022), stroke (Dai et al., 2021; Xu T. et al., 2022), and postoperative neurocognitive disorder (POND) (He et al., 2021; Wu et al., 2021; Zhang M. X. et al., 2022). However, they have failed to manage the aforementioned brain cognitive disorders with effective therapeutics and to uncover largely unknown underlying mechanisms.
In this review, we discussed the effects of circRNAs on various brain neurocognitive disorders as mentioned above. We also found a network of circRNA–miRNA–mRNA for the potential treatment or therapeutics of the aforementioned neurocognitive impaired diseases or conditions.
CircRNA–miRNA–mRNA networks in brain cognitive disorders
Alzheimer's disease
Alzheimer's disease, the most common cause of dementia, is a rising global health issue with tremendous implications. A crucial characteristic of AD is an aberrant accumulation of β-amyloid (Aβ) peptides in the brain, in terms of enhanced cleavage of Aβ precursor protein (APP) by the rate-limiting β-site APP-cleaving enzyme 1 (BACE1) (Shi et al., 2017). The circRNA cerebellar degeneration-related protein 1 antisense (CDR1as, also known as ciRS-7), a gigantic molecule, functions as a miR-7 sponge or inhibitor (Kumar et al., 2017; Li et al., 2019). However, ciRS-7 expression inhibits the translation of nuclear factor kappa B (NF-κB) and induces its cytoplasmic localization, derepressing the expression of ubiquitin carboxyl-terminal hydrolase L1 (UCHL1), which enhances the degradation of APP and BACE1 so as to be available in neuroprotection (Shi et al., 2017). The downregulation of ciRS-7 upregulates miR-7 and lowers the expression of ubiquitin-conjugating enzyme E2A (UBE2A, a location in chr Xq24), which coordinates the clearance of Aβ via proteolysis and contributes to the accumulation of Aβ and the formation of senile plaque deposits (Zhao et al., 2016). However, the trend toward change of consistency relationship between CDR1as/ciRS-7 and miR-7 is still controversial. In addition, in terms of sponging or inhibition of miR-7, ciRS-7 may prevent miR-7 from degradation (Kleaveland et al., 2018).
Serum circHDAC9 was decreased in patients with AD and individuals with mild cognitive impairment. circHDAC9 acts as a miR-138 sponge, decreasing miR-138 expression and reversing the suppression of silent information regulator 1 (Sirt1) and excess production of Aβ in AD (Lu et al., 2019).
Circ_0000950 sponging miR-103 increases the expression of prostaglandin-endoperoxide synthase 2 (PTGS2) and elevates the levels of inflammatory cytokines [interleukin-1β (IL-1β), IL-6, and tumor necrosis factor α (TNF-α)] to inhibit neurite outgrowth and promote neuron apoptosis in AD (Yang et al., 2019). The downregulation of circ_0001588 upregulates miR-211-5p and induces the Sirt1/nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) pathway to prevent oxidative stress in AD (Zhu et al., 2020). CircAXL decreases miR-328 to upregulate the expression of BACE1 in AD (Li et al., 2022). Circ_0003611 downregulates miR-885-5p to aggravate Aβ-induced neuronal injury in AD (Pan et al., 2022). Circ_0005835 promotes the development of AD via regulating miR-576-3p expression (Xu X. et al., 2022).
The networks of circRNA–miRNA–mRNA are involved in mitogen-activated protein kinase (MAPK), mammalian target of rapamycin (mTOR), AMP-activated protein kinase (AMPK), and Wnt signaling pathways in the pathogenesis of AD (Li Y. et al., 2020). Certainly, in the presence of RNA-seq and prediction tools for circRNA bioinformatic analysis, the circRNA–miRNA–mRNA network will indicate one more potential role of epigenetic control over the expression of pathogenic genes in the human central nervous system (CNS) in the development and therapeutic treatment of sporadic AD.
Parkinson's disease
Parkinson's disease, characterized by motor and non-motor symptoms, is also a neurodegenerative disorder. A growing body of research in recent decades has denoted that cognitive decline is a common non-motor symptom of PD (Hall and Lewis, 2019; Leng et al., 2020). With the development of potentially effective treatment, useful biomarkers (such as α-synuclein and some possible circRNAs) of PD may provide early diagnosis, therapeutic monitoring, and prognosis (Hosaka et al., 2019; Liu et al., 2022). The RNA-binding protein FUS acts as a new regulator of circRNA production in motor neurons in mice (Errichelli et al., 2017; D'Anca et al., 2022).
In PD, the neuroprotective role of miR-7 is induced through the alleviation of the suppression of NF-κB by lowering the expression of RelA (a component of NF-κB) due to dopaminergic neurotoxicity (Choi et al., 2014). In addition, miR-7 can target and downregulate α-synuclein, protecting neurons from oxidative stress (Junn et al., 2009; Zhu et al., 2021). circzip-2 sponging miR-60 decreases the expression of protein α-synuclein in the Caenorhabditis elegans model of PD (Kumar et al., 2018). In a mouse model, the circ_0003292/miR-132/Nr4a2 network may be involved in the molecular mechanism of PD (Jia et al., 2020).
In in vivo and in vitro studies, circRNA DLGAP4 (circDLGAP4) exerts a promotion in viability, a reduction in apoptosis, a decline in mitochondrial damage, and an enhancement in autophagy via modulating the miR-134-5p/CREB pathway in PD (Feng et al., 2020). circSAMD4A participates in the apoptosis and autophagy of dopaminergic neurons via the miR-29c-3p-mediated AMPK/mTOR pathway in PD (Wang et al., 2021). circPank1 promotes dopaminergic neuron neurodegeneration through the modulation of the miR-7a-5p/α-syn pathway in PD (Liu et al., 2022). Moreover, circ_0004381 functions as a sponge of miR-185-5p to affect RAC1 expression, contributing to MPP(+)-triggered neuron injury in a cellular model of PD in SK-N-SH cells (Zhang et al., 2022).
Traumatic brain injury
Due to the higher rates of morbidity and mortality, TBI with unclear mechanisms is a serious problem for individuals and society. In the hippocampus of TBI rats, the expressions of circ_006508 and circ_010705 are upregulated, while the expressions of circ_001167 and circ_001168 are downregulated (Xie et al., 2018). In C57BL/6 mice subjected to TBI, increased circRNA chr8_87859283-87904548 blocks the restoration of neurological function after TBI by the chr8_87859283-87904548/mmu-let-7a-5p/CXCR2 axis (Chen et al., 2019). According to the profile of exosomes isolated from the cerebral extracellular space after TBI, 231 significantly dysregulated circRNAs (155 upregulated and 76 downregulated) were on presentation. Pathways of neuronal growth and repair, development, glutamatergic synapse signal transmission, and cyclic guanosine monophosphate–protein kinase G were predicted according to the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) analyses (Zhao et al., 2018).
Circ_0020269 (circHtra1) was significantly upregulated in the brain with TBI. CircHtra1 serves as a miR-3960 sponge, upregulates the levels of GRB10, inhibits cell proliferation, and promotes neuronal apoptosis and NK cell infiltration after TBI (Zheng et al., 2022). After the validation of the polymerase chain reaction (PCR) of 10 circRNAs, circ_009194 was the most upregulated in the hippocampus after TBI. Mechanistically, circ_009194 functions as a sponge for miR-145-3p to regulate Sp1-mediated voltage-gated sodium channel (Nav1.3) in neurological outcomes in TBI (Huang X. J. et al., 2022). circ_010705 (circLrp1b) is significantly upregulated in the brain with TBI induced by controlled cortical impact (CCI). Upregulated circLrp1b as a sponge of miR-27a-3p increases the expression of Dram2 and promotes neurologic impairment, autophagy, and inflammation after TBI (Li H. et al., 2020).
Stroke
Cerebrovascular disease with complicated mechanisms is one of the top three causes of disability-adjusted life-years (DALYs) globally (Collaborators GDH, 2017). The expression of circRNA circ_008018, circ_015350, and circ_016128 was upregulated, while the expression of circ_011137, circ_001729, and circ_006696 was downregulated. Each of these validated circRNAs may have more than 60 binding sites for miRNAs, which may be involved in the predicted pathways of MAPK, the cell cycle, and the regulation of the actin cytoskeleton (Mehta et al., 2017). In ischemic brain stroke, three (1,027 in total) circRNAs (circ_40001, circ_013120, and circ_40806) with the corresponding pathway of Rap1 signaling and Hippo signaling (according to the KEGG and GO analysis) regulate cell survival, death, and recovery through networks of circRNA–miRNA-target genes (Liu et al., 2017). However, the mechanism of circRNAs in the development of stroke remains largely unknown.
Expressions of circRNA Hectd1 (circHectd1) in ischemic stroke tissues from transient middle cerebral artery occlusion (tMCAO) mice and in plasma samples from patients with acute ischemic stroke (AIS) are significantly increased. In tMCAO mice, the knockdown of circHectd1 can significantly decrease cerebral infarct size, neuronal deficits, and astrocyte activation, though miR-142 targets TCDD inducible poly[ADP-ribose] polymerase (TIPARP) and inhibits the astrocyte activation via macroautophagy/autophagy (Han et al., 2018). The levels of circHectd1 are increased in patients with AIS, predicting a much higher risk of AIS recurrence with an area under the curve (AUC) of 0.694 (95% confidence interval (CI): 0.586–0.801) (Peng et al., 2019). The downregulation of circHectd1 induces neuroprotection against ischemic stroke through the miR-133b/TRAF3 pathway (Dai et al., 2021). CircHectd1 regulates ischemic stroke injury via mechanisms involving the regulation of the let-7c-5p/ROCK1 axis (Guo et al., 2022).
Injection of circDLGAP4 can significantly attenuate neurological deficits, infarct size, and blood–brain barrier damage via circDLGAP4/miR-143/Hectd1 axes in tMCAO in a mouse stroke model (Bai et al., 2018). Bioinformatic analysis indicates that the upregulation of circ_015947 could enhance the expression of the predicted sponging miRNAs (miR-188-3p, miR-329-5p, miR-3057-3p, miR-5098, and miR-683), which are involved in apoptosis, metabolism, and the immune-related pathways in the pathogenesis of stroke (Lin et al., 2016). Circ_0025984 ameliorates ischemic stroke injury and protects astrocytes via the miR-143-3p/TET1/ORP150 pathway (Zhou et al., 2021). Overexpression of circ_0000831 is sufficient to inhibit neuroinflammation and vertigo in cerebral ischemia through a miR-16-5p-dependent mechanism (Huang et al., 2022). circSKA3, in an area under the ROC curve of 0.614 (95% CI: 0.546–0.680) in predicting clinical outcomes of patients with AIS, acts as a sponge of miR-6796-5p by regulating the expression of matrix metalloproteinase 9 (Xu T. et al., 2022). Hypoxic pretreated adipose-derived stem cell (ADSC) exosome improves cognitive function by decreasing neuronal damage and shifting microglia from an M1 to M2 phenotype in the hippocampus of AIS via circRps5/miR-124-3p/SIRT7 axes (Yang H. et al., 2022). CircUSP36 attenuates ischemic stroke injury through the miR-139-3p/SMAD3/Bcl2 signal axis (Yang J. et al., 2022). The ratio of serum circRNA-284 to miR-221 may serve as a diagnostic biomarker of carotid plaque rupture and stroke with an AUC of 0.98 (95% CI: 0.96–1.00) (Bazan et al., 2017). As mentioned above, several circRNAs function as both potential therapeutics and biomarkers for ischemic stroke.
Postoperative neurocognitive disorder
During postoperative recovery, patients suffer from neurocognitive disorders. Preclinical neurocognitive disorders before anesthesia and surgery, the early onset of postoperative delirium, and long-lasting PONDs fall under the recommended terminology “perioperative neurocognitive disorders” (Evered et al., 2018). POND is defined by the presence of impaired memory, learning, and executive function after surgery (Migirov et al., 2021; Peden et al., 2021). POND without effective therapeutics and clear mechanisms is becoming a problem due to increased mortality, prolonged hospitalization, reliance on social transfer payments, and decreased quality of life (Eckenhoff et al., 2020; Peden et al., 2021).
The roles of ncRNAs in the development of POND are mentioned in our recent review elsewhere (He et al., 2021). Recent studies demonstrated that circ_089763 may be a crucial circRNA and function as a biomarker in the development of POND (Wang et al., 2019; Gao et al., 2020; Zhou et al., 2020). In serum samples from elderly patients with POND, the expression of circ_061570, circ_001145, and circ_101138 is increased (Gao et al., 2020). However, the mechanisms and effective therapeutics are unclear. ITSN1, a parent gene of circ_061570, plays an important role in early endocytic anomalies and the incidence of AD (Keating et al., 2006; Yu et al., 2008). Circ_001145 can sponge miR-1226-5p to the target gene Itsn1 in terms of circRNA–miRNA–mRNA axes. The network of circ_101138/miR-107/NEDD9 is predicted by Gao et al. (2020). Also, the upregulation of circ_009789 and circ_004229 may act as a sponge of miR-298-5p to upregulate the expression of Prkcb and Zbtb4 in the hippocampus of aging mice. Here, PKC signaling pathway, neural cell apoptosis, and glycolipid metabolism pathway are involved in the development of working memory dysfunction after surgery (Zhang M. X. et al., 2022).
Additionally, circ_101138 could regulate miR-376a/b-3p targeting HAS2 (Gao et al., 2020), which was associated with the pathogenesis of neuropathologic changes (Reed et al., 2019) and tau protein in AD-related neurocognitive dysfunction (Li et al., 2017). Additionally, circ_101138 could regulate miR-107, which was downregulated and a marker of the neurodegenerative process in AD concerning the Aβ metabolism and the inordinate cell cycle (Prendecki et al., 2019). However, the downregulation of miR-107 exerts the upregulation of SYK and worsens spatial memory in AD mice by activating the NF-κB signaling pathway (Hu et al., 2019). Here, circ_101138/miR-107/Syk might be another network of circRNA–miRNA–mRNA in the development of both POND and AD. A network of circ_101138/miR-107/Syk may explain the changes of POND in AD.
In another cohort study on geriatrics with no previous diagnosis of dementia, the level of Aβ1-42 in cerebral spinal fluid was the strongest independent predictor of postoperative delirium (included in PONDs) after elective arthroplasty in an aging population (Cunningham et al., 2019). Aβ is one of the key molecules involved in neurodegenerative diseases, and its degradation is partially regulated by the aforementioned networks of ciRS-7/miR-7a/Uchl1 and ciRS-7/miR-7a/Ubea2 (Zhao et al., 2016; Shi et al., 2017). As mentioned above, circHDAC9/miR-138/Sirt1 was involved in AD (Lu et al., 2019), while a decrease in Sirt1 was associated with improved postoperative cognition after cardiac surgery (Shi et al., 2020). In addition, circRNAs were engaged against POND by dexmedetomidine (Cao et al., 2020). Thus, the potential and protective roles of the circRNA–miRNA–mRNA axes would be studied in the future.
Conclusions and perspectives
The crosstalk between circRNA, miRNA, and mRNA (or proteins) through one or more circRNA–miRNA–mRNA networks indicates the complicated and dynamic mechanisms of brain cognitive disorders including AD (Zhao et al., 2016; Lu et al., 2019; Yang et al., 2019; Zhu et al., 2020; Li et al., 2022; Pan et al., 2022; Xu X. et al., 2022), PD (Kumar et al., 2018; Feng et al., 2020; Wang et al., 2021; Liu et al., 2022; Zhang et al., 2022), TBI (Chen et al., 2019; Li H. et al., 2020; Huang X. J. et al., 2022; Zheng et al., 2022), stroke (Bai et al., 2018; Han et al., 2018; Zhou et al., 2021; Guo et al., 2022; Huang et al., 2022; Xu T. et al., 2022; Yang H. et al., 2022; Yang J. et al., 2022), and POND (Gao et al., 2020) (Table 1). In summary, circRNAs act as sponging-like roles in transcription and posttranscription in the novel regulation processes of gene expression. However, none of the aforementioned studies were able to clearly determine the exact role of circRNA–miRNA–mRNA axes in the pathogenesis and development of brain disorders with cognitive dysfunction or impairment (Figure 2).
Table 1. Circular RNAs (CircRNAs) in various brain cognitive disorders.
Figure 2. Regulatory networks of circRNA–miRNA–mRNA in various brain disorders. Changes in the regulatory networks of circRNA–miRNA–mRNA and potential signaling pathways are presented.
Different circRNAs sponge different miRNAs under various brain disorders (Figure 2). Meanwhile, the same circDLGAP4 can be involved in sponging different miRNAs, such as miR-143 in stroke (Bai et al., 2018) and miR-134-5p in PD (Feng et al., 2020). As it indicates that similar circRNA sponging different miRNAs may occur in different diseases. However, in similar brain disorders or conditions, circHectd1 can sponge different miRNAs, including miR-133b, let-7c-5p, and miR-142 (Han et al., 2018; Dai et al., 2021; Guo et al., 2022), indicating that one disease may embrace different pathways under different conditions. However, how should we check and determine which is the best pathway (Gao et al., 2020)?
The aforementioned studies on the circRNA–miRNA–mRNA network suggest that circRNAs as endogenous RNAs (ceRNAs) play important roles in discovering the pathogenesis and development of brain disorders in the future. Recently, some studies indicate that a subset of circRNAs has been considered as codes for proteins (Ma et al., 2020; Sinha et al., 2021). However, the available evidence shows that circRNA translation is not an efficient event. Herein, many more studies on circRNA–miRNA–mRNA networks are needed to update and expand our knowledge about increasing effective strategies to protect individuals from these brain disorders.
Author contributions
Conceptualization, writing—original draft, and funding acquisition: LH. Formal analysis: LH, FZ, and YZ. Writing—review and editing: LH and ML. All authors had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis, contributed to the article, and approved the submitted version.
Funding
This work was supported by the Chuncheng Youth Top-notch Talent Support Program (2020), the Health and Family Planning Commission of Yunnan province (H-2017047), and partially by the National Natural Science Foundation of China (81860208).
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
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References
Bai, Y., Zhang, Y., Han, B., Yang, L., Chen, X., Huang, R., et al. (2018). Circular RNA DLGAP4 ameliorates ischemic stroke outcomes by targeting miR-143 to regulate endothelial-mesenchymal transition associated with blood-brain barrier integrity. J. Neurosci. 38, 32–50. doi: 10.1523/jneurosci.1348-17.2017
Bazan, H. A., Hatfield, S. A., Brug, A., Brooks, A. J., Lightell, D. J. Jr., and Woods, T. C. (2017). Carotid plaque rupture is accompanied by an increase in the ratio of serum circR-284 to miR-221 levels. Circ. Cardiovasc. Genet. 10, e001720. doi: 10.1161/circgenetics.117.001720
Cao, C., Deng, F., and Hu, Y. (2020). Dexmedetomidine alleviates postoperative cognitive dysfunction through circular RNA in aged rats. Biotechnology 10, 176. doi: 10.1007/s13205-020-2163-0
Chen, Y., Yao, L., Tang, Y., Jhong, J. H., Wan, J., Chang, J., et al. (2022). CircNet 2.0: an updated database for exploring circular RNA regulatory networks in cancers. Nucleic Acids Res. 50, D93–d101. doi: 10.1093/nar/gkab1036
Chen, Z., Wang, H., Zhong, J., Yang, J., Darwazeh, R., Tian, X., et al. (2019). Significant changes in circular RNA in the mouse cerebral cortex around an injury site after traumatic brain injury. Exp. Neurol. 313, 37–48. doi: 10.1016/j.expneurol.2018.12.003
Choi, D. C., Chae, Y. J., Kabaria, S., Chaudhuri, A. D., Jain, M. R., Li, H., et al. (2014). MicroRNA-7 protects against 1-methyl-4-phenylpyridinium-induced cell death by targeting RelA. J. Neurosci. 34, 12725–12737. doi: 10.1523/jneurosci.0985-14.2014
Collaborators GDH (2017). Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet 390, 1260–1344. doi: 10.1016/s0140-6736(17)32130-x
Cunningham, E. L., McGuinness, B., McAuley, D. F., Toombs, J., Mawhinney, T., O'Brien, S., et al. (2019). CSF beta-amyloid 1-42 concentration predicts delirium following elective arthroplasty surgery in an observational cohort study. Ann. Surg. 269, 1200–1205. doi: 10.1097/sla.0000000000002684
Dai, Q., Ma, Y., Xu, Z., Zhang, L., Yang, H., Liu, Q., et al. (2021). Downregulation of circular RNA HECTD1 induces neuroprotection against ischemic stroke through the microRNA-133b/TRAF3 pathway. Life Sci. 264, 118626. doi: 10.1016/j.lfs.2020.118626
D'Anca, M., Buccellato, F. R., Fenoglio, C., and Galimberti, D. (2022). Circular RNAs: emblematic players of neurogenesis and neurodegeneration. Int. J. Mol. Sci. 23, 4134. doi: 10.3390/ijms23084134
Dong, R., Ma, X. K., Li, G. W., and Yang, L. (2018). CIRCpedia v2: an updated database for comprehensive circular RNA annotation and expression comparison. Genom. Proteom. Bioinform. 16, 226–233. doi: 10.1016/j.gpb.2018.08.001
Eckenhoff, R. G., Maze, M., Xie, Z., Culley, D. J., Goodlin, S. J., Zuo, Z., et al. (2020). Perioperative neurocognitive disorder: state of the preclinical science. Anesthesiology 132, 55–68. doi: 10.1097/aln.0000000000002956
Errichelli, L., Dini Modigliani, S., Laneve, P., Colantoni, A., Legnini, I., Capauto, D., et al. (2017). FUS affects circular RNA expression in murine embryonic stem cell-derived motor neurons. Nat. Commun. 8, 14741. doi: 10.1038/ncomms14741
Evered, L., Silbert, B., Knopman, D. S., Scott, D. A., DeKosky, S. T., Rasmussen, L. S., et al. (2018). Recommendations for the nomenclature of cognitive change associated with anaesthesia and surgery−2018. Anesthesiology 129, 872–879. doi: 10.1097/aln.0000000000002334
Feng, Z., Zhang, L., Wang, S., and Hong, Q. (2020). Circular RNA circDLGAP4 exerts neuroprotective effects via modulating miR-134-5p/CREB pathway in Parkinson's disease. Biochem. Biophys. Res. Commun. 522, 388–394. doi: 10.1016/j.bbrc.2019.11.102
Gao, R., Chen, C., Zhao, Q., Li, M., Wang, Q., Zhou, L., et al. (2020). Identification of the potential key circular RNAs in elderly patients with postoperative cognitive dysfunction. Front. Aging Neurosci. 12, 165. doi: 10.3389/fnagi.2020.00165
Guo, Q., Guo, T., Sun, Y., and Chen, T. (2022). Circ_HECTD1 regulates cerebral ischemia injury via mechanisms involving the regulation of let-7c-5p/ROCK1 axis. Neuroreport 33, 13–22. doi: 10.1097/wnr.0000000000001743
Hall, J. M., and Lewis, S. J. G. (2019). Neural correlates of cognitive impairment in parkinson's disease: a review of structural MRI findings. Int. Rev. Neurobiol. 144, 1–28. doi: 10.1016/bs.irn.2018.09.009
Han, B., Zhang, Y., Zhang, Y., Bai, Y., Chen, X., Huang, R., et al. (2018). Novel insight into circular RNA HECTD1 in astrocyte activation via autophagy by targeting MIR142-TIPARP: implications for cerebral ischemic stroke. Autophagy 14, 1164–1184. doi: 10.1080/15548627.2018.1458173
Hansen, T. B., Jensen, T. I., Clausen, B. H., Bramsen, J. B., Finsen, B., Damgaard, C. K., et al. (2013). Natural RNA circles function as efficient microRNA sponges. Nature 495, 384–388. doi: 10.1038/nature11993
He, L., Zhang, F., Zhu, Y., and Lu, M. (2021). Noncoding RNAs: novel insights into postoperative neurocognitive disorders. ACS Chem. Neurosci. 12, 1480–1486. doi: 10.1021/acschemneuro.1c00148
Hosaka, T., Yamashita, T., Tamaoka, A., and Kwak, S. (2019). Extracellular RNAs as biomarkers of sporadic amyotrophic lateral sclerosis and other neurodegenerative diseases. Int. J. Mol. Sci. 20, 3148. doi: 10.3390/ijms20133148
Hu, W., Wen, L., Cao, F., and Wang, Y. (2019). Down-regulation of MIR-107 worsen spatial memory by suppressing SYK expression and inactivating NF-?B signaling pathway. Curr. Alzheimer Res. 16, 135–145. doi: 10.2174/1567205016666181212154347
Huang, R., Zhang, W., Li, W., Gao, Y., Zheng, D., and Bi, G. (2022). Overexpressing circ_0000831 is sufficient to inhibit neuroinflammation and vertigo in cerebral ischemia through a miR-16-5p-dependent mechanism. Exp. Neurol. 353, 114047. doi: 10.1016/j.expneurol.2022.114047
Huang, X. J., Su, G. J., Wu, C. W., Sha, X. S., Zou, J. F., Liu, X. S., et al. (2022). Knockdown of rno_circRNA_009194 improves outcomes in traumatic brain injury rats through inhibiting voltage-gated sodium channel Nav1.3. J. Neurotrauma 39, 196–210. doi: 10.1089/neu.2020.7520
Jia, E., Zhou, Y., Liu, Z., Wang, L., Ouyang, T., Pan, M., et al. (2020). Transcriptomic profiling of circular RNA in different brain regions of Parkinson's disease in a mouse model. Int. J. Mol. Sci. 21, 3006. doi: 10.3390/ijms21083006
Junn, E., Lee, K. W., Jeong, B. S., Chan, T. W., Im, J. Y., and Mouradian, M. M. (2009). Repression of alpha-synuclein expression and toxicity by microRNA-7. Proc. Natl. Acad. Sci. USA. 106, 13052–13057. doi: 10.1073/pnas.0906277106
Keating, D. J., Chen, C., and Pritchard, M. A. (2006). Alzheimer's disease and endocytic dysfunction: clues from the Down syndrome-related proteins, DSCR1 and ITSN1. Ageing Res. Rev. 5, 388–401. doi: 10.1016/j.arr.2005.11.001
Kleaveland, B., Shi, C. Y., Stefano, J., and Bartel, D. P. (2018). A network of noncoding regulatory RNAs acts in the mammalian brain. Cell 174, 350-362.e317. doi: 10.1016/j.cell.2018.05.022
Kristensen, L. S., Andersen, M. S., Stagsted, L. V. W., Ebbesen, K. K., Hansen, T. B., and Kjems, J. (2019). The biogenesis, biology and characterization of circular RNAs. Nat. Rev. Genet. 20, 675–691. doi: 10.1038/s41576-019-0158-7
Kumar, L., Shamsuzzama, H. R., Baghel, T., and Nazir, A. (2017). Circular RNAs: the emerging class of non-coding RNAs and their potential role in human neurodegenerative diseases. Mol. Neurobiol. 54, 7224–7234. doi: 10.1007/s12035-016-0213-8
Kumar, L., Shamsuzzama, J., adiya, P., Haque, R., Shukla, S., and Nazir, A. (2018). Functional characterization of novel circular RNA molecule, circzip-2 and its synthesizing gene zip-2 in C. elegans model of Parkinson's disease. Mol Neurobiol 55, 6914–6926. doi: 10.1007/s12035-018-0903-5
Leng, B., Sun, H., Zhao, J., Liu, Y., Shen, T., Liu, W., et al. (2020). Plasma exosomal prion protein levels are correlated with cognitive decline in PD patients. Neurosci. Lett. 723, 134866. doi: 10.1016/j.neulet.2020.134866
Li, H., Lu, C., Yao, W., Xu, L., Zhou, J., and Zheng, B. (2020). Dexmedetomidine inhibits inflammatory response and autophagy through the circLrp1b/miR-27a-3p/Dram2 pathway in a rat model of traumatic brain injury. Aging (Albany NY) 12, 21687–21705. doi: 10.18632/aging.103975
Li, H. M., Ma, X. L., and Li, H. G. (2019). Intriguing circles: conflicts and controversies in circular RNA research. Wiley Interdiscip. Rev. RNA 10, e1538. doi: 10.1002/wrna.1538
Li, Y., Han, X., Fan, H., Sun, J., Ni, M., Zhang, L., et al. (2022). Circular RNA AXL increases neuron injury and inflammation through targeting microRNA-328 mediated BACE1 in Alzheimer's disease. Neurosci. Lett. 776, 136531. doi: 10.1016/j.neulet.2022.136531
Li, Y., Li, Z. X., Jin, T., Wang, Z. Y., and Zhao, P. (2017). Tau pathology promotes the reorganization of the extracellular matrix and inhibits the formation of perineuronal nets by regulating the expression and the distribution of hyaluronic acid synthases. J. Alzheimers. Dis. 57, 395–409. doi: 10.3233/jad-160804
Li, Y., Lv, Z., Zhang, J., Ma, Q., Li, Q., Song, L., et al. (2020). Profiling of differentially expressed circular RNAs in peripheral blood mononuclear cells from Alzheimer's disease patients. Metab. Brain Dis. 35, 201–213. doi: 10.1007/s11011-019-00497-y
Lin, S. P., Ye, S., Long, Y., Fan, Y., Mao, H. F., Chen, M. T., et al. (2016). Circular RNA expression alterations are involved in OGD/R-induced neuron injury. Biochem. Biophys. Res. Commun. 471, 52–56. doi: 10.1016/j.bbrc.2016.01.183
Liu, C., Zhang, C., Yang, J., Geng, X., Du, H., Ji, X., et al. (2017). Screening circular RNA expression patterns following focal cerebral ischemia in mice. Oncotarget 8, 86535–86547. doi: 10.18632/oncotarget.21238
Liu, Q., Li, Q., Zhang, R., Wang, H., Li, Y., Liu, Z., et al. (2022). circ-Pank1 promotes dopaminergic neuron neurodegeneration through modulating miR-7a-5p/α-syn pathway in Parkinson's disease. Cell Death Dis. 13, 477. doi: 10.1038/s41419-022-04934-2
Lu, Y., Tan, L., and Wang, X. (2019). Circular HDAC9/microRNA-138/Sirtuin-1 pathway mediates synaptic and amyloid precursor protein processing deficits in Alzheimer's disease. Neurosci. Bull. 35, 877–888. doi: 10.1007/s12264-019-00361-0
Ma, N., Tie, C., Yu, B., Zhang, W., and Wan, J. (2020). Circular RNAs regulate its parental genes transcription in the AD mouse model using two methods of library construction. FASEB J. 34, 10342–10356. doi: 10.1096/fj.201903157R
Mehta, S. L., Pandi, G., and Vemuganti, R. (2017). Circular RNA expression profiles alter significantly in mouse brain after transient focal ischemia. Stroke 48, 2541–2548. doi: 10.1161/strokeaha.117.017469
Migirov, A., Chahar, P., and Maheshwari, K. (2021). Postoperative delirium and neurocognitive disorders. Curr. Opin. Crit. Care 27, 686–693. doi: 10.1097/mcc.0000000000000882
Pan, W., Hu, Y., Wang, L., and Li, J. (2022). Circ_0003611 acts as a miR-885-5p sponge to aggravate the amyloid-β-induced neuronal injury in Alzheimer's disease. Metab. Brain Dis. 37, 961–971. doi: 10.1007/s11011-022-00912-x
Peden, C. J., Miller, T. R., Deiner, S. G., Eckenhoff, R. G., and Fleisher, L. A. (2021). Improving perioperative brain health: an expert consensus review of key actions for the perioperative care team. Br. J. Anaesth. 126, 423–432. doi: 10.1016/j.bja.2020.10.037
Peng, X., Jing, P., Chen, J., and Xu, L. (2019). The role of circular RNA HECTD1 expression in disease risk, disease severity, inflammation, and recurrence of acute ischemic stroke. J. Clin. Lab. Anal. 33, e22954. doi: 10.1002/jcla.22954
Prendecki, M., Florczak-Wyspianska, J., Kowalska, M., Ilkowski, J., Grzelak, T., Bialas, K., et al. (2019). APOE genetic variants and apoE, miR-107 and miR-650 levels in Alzheimer's disease. Folia Neuropathol. 57, 106–116. doi: 10.5114/fn.2019.84828
Reed, M. J., Damodarasamy, M., Pathan, J. L., Chan, C. K., Spiekerman, C., Wight, T. N., et al. (2019). Increased hyaluronan and TSG-6 in association with neuropathologic changes of Alzheimer's disease. J. Alzheimers. Dis. 67, 91–102. doi: 10.3233/jad-180797
Salim, U., Kumar, A., Kulshreshtha, R., and Vivekanandan, P. (2022). Biogenesis, characterization, and functions of mirtrons. Wiley Interdiscip. Rev. RNA 13, e1680. doi: 10.1002/wrna.1680
Salmena, L., Poliseno, L., Tay, Y., Kats, L., and Pandolfi, P. P. (2011). A ceRNA hypothesis: the Rosetta Stone of a hidden RNA language? Cell 146, 353–358. doi: 10.1016/j.cell.2011.07.014
Shi, J., Zou, X., Jiang, K., and Wang, F. (2020). SIRT1 mediates improvement of cardiac surgery-induced postoperative cognitive dysfunction via the TLR4/NF-κB pathway. World J. Biol. Psychiatry 21, 757–765. doi: 10.1080/15622975.2019.1656820
Shi, Z., Chen, T., Yao, Q., Zheng, L., Zhang, Z., Wang, J., et al. (2017). The circular RNA ciRS-7 promotes APP and BACE1 degradation in an NF-kappaB-dependent manner. FEBS J. 284, 1096–1109. doi: 10.1111/febs.14045
Sinha, T., Panigrahi, C., Das, D., and Chandra Panda, A. (2021). Circular RNA translation, a path to hidden proteome. Wiley Interdiscip Rev RNA 2021:e1685. doi: 10.1002/wrna.1685
Wang, M., Su, P., Liu, Y., Zhang, X., Yan, J., An, X., et al. (2019). Abnormal expression of circRNA_089763 in the plasma exosomes of patients with post-operative cognitive dysfunction after coronary artery bypass grafting. Mol. Med. Rep. 20, 2549–2562. doi: 10.3892/mmr.2019.10521
Wang, W., Lv, R., Zhang, J., and Liu, Y. (2021). circSAMD4A participates in the apoptosis and autophagy of dopaminergic neurons via the miR-29c-3p-mediated AMPK/mTOR pathway in Parkinson's disease. Mol. Med. Rep. 24, 12179. doi: 10.3892/mmr.2021.12179
Wu, W., Peng, Y., Zhou, J., Zhang, X., Cao, L., Lin, W. J., et al. (2021). Identification of the potential gene regulatory networks and therapeutics in aged mice with postoperative neurocognitive disorder. Front. Neurosci. 15, 689188. doi: 10.3389/fnins.2021.689188
Xie, B. S., Wang, Y. Q., Lin, Y., Zhao, C. C., Mao, Q., Feng, J. F., et al. (2018). Circular RNA expression profiles alter significantly after traumatic brain injury in rats. J. Neurotrauma 35, 1659–1666. doi: 10.1089/neu.2017.5468
Xu, T., Li, Y., Zhu, N., Su, Y., Li, J., and Ke, K. (2022). circSKA3 acts as a sponge of miR-6796-5p to be associated with outcomes of ischemic stroke by regulating matrix metalloproteinase 9 expression. Eur. J. Neurol. 29, 486–495. doi: 10.1111/ene.15164
Xu, X., Gu, D., Xu, B., Yang, C., and Wang, L. (2022). Circular RNA circ_0005835 promotes promoted neural stem cells proliferation and differentiate to neuron and inhibits inflammatory cytokines levels through miR-576-3p in Alzheimer's disease. Environ. Sci. Pollut. Res. Int. 29, 35934–35943. doi: 10.1007/s11356-021-17478-3
Yang, H., Tu, Z., Yang, D., Hu, M., Zhou, L., Li, Q., et al. (2022). Exosomes from hypoxic pre-treated ADSCs attenuate acute ischemic stroke-induced brain injury via delivery of circ-Rps5 and promote M2 microglia/macrophage polarization. Neurosci. Lett. 769, 136389. doi: 10.1016/j.neulet.2021.136389
Yang, H., Wang, H., Shang, H., Chen, X., Yang, S., Qu, Y., et al. (2019). Circular RNA circ_0000950 promotes neuron apoptosis, suppresses neurite outgrowth and elevates inflammatory cytokines levels via directly sponging miR-103 in Alzheimer's disease. Cell Cycle 18, 2197–2214. doi: 10.1080/15384101.2019.1629773
Yang, J., He, W., Gu, L., Long, J., Zhu, L., Zhang, R., et al. (2022). CircUSP36 attenuates ischemic stroke injury through the miR-139-3p/SMAD3/Bcl2 signal axis. Clin. Sci. (Lond) 136, 953–971. doi: 10.1042/cs20220157
Yesharim, L., Mojbafan, M., and Abiri, M. (2021). Hints from the cellular functions to the practical outlook of circular RNAs. Front. Genet. 12, 679446. doi: 10.3389/fgene.2021.679446
Yu, Y., Chu, P. Y., Bowser, D. N., Keating, D. J., Dubach, D., Harper, I., et al. (2008). Mice deficient for the chromosome 21 ortholog Itsn1 exhibit vesicle-trafficking abnormalities. Hum. Mol. Genet. 17, 3281–3290. doi: 10.1093/hmg/ddn224
Zhang, H., Wang, C., and Zhang, X. (2022). Circular RNA hsa_circ_0004381 promotes neuronal injury in Parkinson's disease cell model by miR-185-5p/RAC1 axis. Neurotox. Res. 40, 1007–1019. doi: 10.1007/s12640-022-00525-3
Zhang, M. X., Lin, J. R., Yang, S. T., Zou, J., Xue, Y., Feng, C. Z., et al. (2022). Characterization of circRNA-associated-ceRNA networks involved in the pathogenesis of postoperative cognitive dysfunction in aging mice. Front. Aging Neurosci. 14, 727805. doi: 10.3389/fnagi.2022.727805
Zhao, R. T., Zhou, J., Dong, X. L., Bi, C. W., Jiang, R. C., Dong, J. F., et al. (2018). Circular ribonucleic acid expression alteration in exosomes from the brain extracellular space after traumatic brain injury in mice. J. Neurotrauma 35, 2056–2066. doi: 10.1089/neu.2017.5502
Zhao, Y., Alexandrov, P. N., Jaber, V., and Lukiw, W. J. (2016). Deficiency in the ubiquitin conjugating enzyme UBE2A in Alzheimer's disease (AD) is linked to deficits in a natural circular miRNA-7 sponge (circRNA; ciRS-7). Genes (Basel) 7, 116. doi: 10.3390/genes7120116
Zheng, P., Shu, L., Ren, D., Kuang, Z., Zhang, Y., and Wan, J. (2022). circHtra1/miR-3960/GRB10 axis promotes neuronal loss and immune deficiency in traumatic brain injury. Oxid. Med. Cell. Longev. 2022, 3522492. doi: 10.1155/2022/3522492
Zhou, D., Huang, Z., Zhu, X., Hong, T., and Zhao, Y. (2021). Circular RNA 0025984 ameliorates ischemic stroke injury and protects astrocytes through miR-143-3p/TET1/ORP150 pathway. Mol. Neurobiol. 58, 5937–5953. doi: 10.1007/s12035-021-02486-8
Zhou, H., Li, F., Ye, W., Wang, M., Zhou, X., Feng, J., et al. (2020). Correlation between plasma circRNA-089763 and postoperative cognitive dysfunction in elderly patients undergoing non-cardiac surgery. Front. Behav. Neurosci. 14, 587715. doi: 10.3389/fnbeh.2020.587715
Zhu, R., Qi, X., Liu, C., Wang, D., Li, L., Liu, X., et al. (2020). The silent information regulator 1 pathway attenuates ROS-induced oxidative stress in Alzheimer's disease. J. Integr. Neurosci. 19, 321–332. doi: 10.31083/j.jin.2020.02.1151
Keywords: circular RNAs, cognitive dysfunction, neurocognitive, network, ceRNA
Citation: He L, Zhang F, Zhu Y and Lu M (2022) A crosstalk between circular RNA, microRNA, and messenger RNA in the development of various brain cognitive disorders. Front. Mol. Neurosci. 15:960657. doi: 10.3389/fnmol.2022.960657
Received: 03 June 2022; Accepted: 28 July 2022;
Published: 18 October 2022.
Edited by:
Nan Wu, University of Toronto, CanadaReviewed by:
Sema MISIR, Cumhuriyet University, TurkeyQiwei Yang, Second Affiliated Hospital of Jilin University, China
Copyright © 2022 He, Zhang, Zhu and Lu. 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: Liang He, hauliang@163.com; Meilin Lu, cc21316@163.com
†ORCID: Liang He orcid.org/0000-0001-7246-4072