Abstract
Traumatic brain injury (TBI) and spinal cord injury (SCI) are two main central nervous system (CNS) traumas, caused by external physical insults. Both injuries have devastating effects on the quality of life, and there is no effective therapy at present. Notably, gene expression profiling using bulk RNA sequencing (RNA-Seq) and single-cell RNA-Seq (scRNA-Seq) have revealed significant changes in many coding and non-coding genes, as well as important pathways in SCI and TBI. Particularly, recent studies have revealed that long non-coding RNAs (lncRNAs) with lengths greater than 200 nucleotides and without protein-coding potential have tissue- and cell type-specific expression pattern and play critical roles in CNS injury by gain- and loss-of-function approaches. LncRNAs have been shown to regulate protein-coding genes or microRNAs (miRNAs) directly or indirectly, participating in processes including inflammation, glial activation, cell apoptosis, and vasculature events. Therefore, lncRNAs could serve as potential targets for the diagnosis, treatment, and prognosis of SCI and TBI. In this review, we highlight the recent progress in transcriptome studies of SCI and TBI and insights into molecular mechanisms.
Similar content being viewed by others
Availability of data and material
Not applicable.
References
Injury GBDTB, Spinal Cord Injury C (2019) Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol 18(1):56–87. https://doi.org/10.1016/S1474-4422(18)30415-0
Ng SY, Lee AYW (2019) Traumatic brain injuries: pathophysiology and potential therapeutic targets. Front Cell Neurosci 13:528. https://doi.org/10.3389/fncel.2019.00528
Jassam YN, Izzy S, Whalen M, McGavern DB, El Khoury J (2017) Neuroimmunology of traumatic brain injury: time for a paradigm shift. Neuron 95(6):1246–1265. https://doi.org/10.1016/j.neuron.2017.07.010
Duan H, Ge W, Zhang A, Xi Y, Chen Z, Luo D, Cheng Y, Fan KS, Horvath S, Sofroniew MV, Cheng L, Yang Z, Sun YE, Li X (2015) Transcriptome analyses reveal molecular mechanisms underlying functional recovery after spinal cord injury. Proc Natl Acad Sci USA 112(43):13360–13365. https://doi.org/10.1073/pnas.1510176112
Wei H, Wu X, You Y, Duran RC, Zheng Y, Narayanan KL, Hai B, Li X, Tallapragada N, Prajapati TJ, Kim DH, Deneen B, Cao QL, Wu JQ (2021) Systematic analysis of purified astrocytes after SCI unveils Zeb2os function during astrogliosis. Cell Rep 34(5):108721. https://doi.org/10.1016/j.celrep.2021.108721
Duran RC, Yan H, Zheng Y, Huang X, Grill R, Kim DH, Cao Q, Wu JQ (2017) The systematic analysis of coding and long non-coding RNAs in the sub-chronic and chronic stages of spinal cord injury. Sci Rep 7:41008. https://doi.org/10.1038/srep41008
Chen K, Deng S, Lu H, Zheng Y, Yang G, Kim D, Cao Q, Wu JQ (2013) RNA-seq characterization of spinal cord injury transcriptome in acute/subacute phases: a resource for understanding the pathology at the systems level. PLoS ONE 8(8):e72567. https://doi.org/10.1371/journal.pone.0072567
Zhou H, Shi Z, Kang Y, Wang Y, Lu L, Pan B, Liu J, Li X, Liu L, Wei Z, Kong X, Feng S (2018) Investigation of candidate long noncoding RNAs and messenger RNAs in the immediate phase of spinal cord injury based on gene expression profiles. Gene 661:119–125. https://doi.org/10.1016/j.gene.2018.03.074
Shi Z, Ning G, Zhang B, Yuan S, Zhou H, Pan B, Li J, Wei Z, Cao F, Kong X, Feng S (2019) Signatures of altered long noncoding RNAs and messenger RNAs expression in the early acute phase of spinal cord injury. J Cell Physiol 234(6):8918–8927. https://doi.org/10.1002/jcp.27560
Ding Y, Song Z, Liu J (2016) Aberrant LncRNA expression profile in a contusion spinal cord injury mouse model. Biomed Res Int 2016:9249401. https://doi.org/10.1155/2016/9249401
Meng Q, Zhuang Y, Ying Z, Agrawal R, Yang X, Gomez-Pinilla F (2017) Traumatic brain injury induces genome-wide transcriptomic, methylomic, and network perturbations in brain and blood predicting neurological disorders. EBioMedicine 16:184–194. https://doi.org/10.1016/j.ebiom.2017.01.046
Arneson D, Zhang G, Ying Z, Zhuang Y, Byun HR, Ahn IS, Gomez-Pinilla F, Yang X (2018) Single cell molecular alterations reveal target cells and pathways of concussive brain injury. Nat Commun 9(1):3894. https://doi.org/10.1038/s41467-018-06222-0
Carninci P, Kasukawa T, Katayama S et al (2005) The transcriptional landscape of the mammalian genome. Science 309(5740):1559–1563. https://doi.org/10.1126/science.1112014
Cabili MN, Trapnell C, Goff L, Koziol M, Tazon-Vega B, Regev A, Rinn JL (2011) Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev 25(18):1915–1927. https://doi.org/10.1101/gad.17446611
Consortium EP, Birney E, Stamatoyannopoulos JA et al (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447(7146):799–816. https://doi.org/10.1038/nature05874
Cuevas-Diaz Duran R, Wei H, Wu JQ (2017) Single-cell RNA-sequencing of the brain. Clin Transl Med 6(1):20. https://doi.org/10.1186/s40169-017-0150-9
Dong X, You Y, Wu JQ (2016) Building an RNA sequencing transcriptome of the central nervous system. Neuroscientist 22(6):579–592. https://doi.org/10.1177/1073858415610541
Narayanan KL, Wu X, Wei H, Wu JQ (2020) Evolving roles of long noncoding RNAs. The Chemical biology of long noncoding RNAs. Springer, pp 59–84
Redon S, Reichenbach P, Lingner J (2010) The non-coding RNA TERRA is a natural ligand and direct inhibitor of human telomerase. Nucleic Acids Res 38(17):5797–5806. https://doi.org/10.1093/nar/gkq296
Wang KC, Chang HY (2011) Molecular mechanisms of long noncoding RNAs. Mol Cell 43(6):904–914. https://doi.org/10.1016/j.molcel.2011.08.018
Rinn JL, Kertesz M, Wang JK, Squazzo SL, Xu X, Sa B, Goodnough LH, Ja H, Farnham PJ, Segal E, Chang HY (2007) Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs. Cell 129:1311–1323. https://doi.org/10.1016/j.cell.2007.05.022
Cuevas-Diaz Duran R, Wei H, Kim DH, Wu JQ (2019) Invited Review: Long non-coding RNAs: important regulators in the development, function and disorders of the central nervous system. Neuropathol Appl Neurobiol 45(6):538–556. https://doi.org/10.1111/nan.12541
Kim TK, Hemberg M, Gray JM, Costa AM, Bear DM, Wu J, Harmin DA, Laptewicz M, Barbara-Haley K, Kuersten S, Markenscoff-Papadimitriou E, Kuhl D, Bito H, Worley PF, Kreiman G, Greenberg ME (2010) Widespread transcription at neuronal activity-regulated enhancers. Nature 465(7295):182–187. https://doi.org/10.1038/nature09033
Zhang L, Wang H (2019) Long non-coding RNA in CNS injuries: a new target for therapeutic intervention. Mol Ther Nucleic Acids 17:754–766. https://doi.org/10.1016/j.omtn.2019.07.013
Amaral PP, Mattick JS (2008) Noncoding RNA in development. Mamm Genome 19(7–8):454–492. https://doi.org/10.1007/s00335-008-9136-7
Sauvageau M, Goff LA, Lodato S, Bonev B, Groff AF, Gerhardinger C, Sanchez-Gomez DB, Hacisuleyman E, Li E, Spence M, Liapis SC, Mallard W, Morse M, Swerdel MR, D’Ecclessis MF, Moore JC, Lai V, Gong G, Yancopoulos GD, Frendewey D, Kellis M, Hart RP, Valenzuela DM, Arlotta P, Rinn JL (2013) Multiple knockout mouse models reveal lincRNAs are required for life and brain development. Elife 2:e01749. https://doi.org/10.7554/eLife.01749
Cuevas-Diaz Duran R, Wang CY, Zheng H, Deneen B, Wu JQ (2019) Brain region-specific gene signatures revealed by distinct astrocyte subpopulations unveil links to glioma and neurodegenerative diseases. eNeuro. https://doi.org/10.1523/ENEURO.0288-18.2019
Dong X, Chen K, Cuevas-Diaz Duran R, You Y, Sloan SA, Zhang Y, Zong S, Cao Q, Barres BA, Wu JQ (2015) Comprehensive identification of long non-coding RNAs in purified cell types from the brain reveals functional LncRNA in OPC fate determination. PLoS Genet 11(12):e1005669. https://doi.org/10.1371/journal.pgen.1005669
Salta E, De Strooper B (2017) Noncoding RNAs in neurodegeneration. Nat Rev Neurosci 18(10):627–640. https://doi.org/10.1038/nrn.2017.90
Pastori C, Wahlestedt C (2012) Involvement of long noncoding RNAs in diseases affecting the central nervous system. RNA Biol 9(6):860–870. https://doi.org/10.4161/rna.20482
He D, Wang J, Lu Y, Deng Y, Zhao C, Xu L, Chen Y, Hu YC, Zhou W, Lu QR (2017) lncRNA functional networks in oligodendrocytes reveal stage-specific myelination control by an lncOL1/Suz12 complex in the CNS. Neuron 93(2):362–378. https://doi.org/10.1016/j.neuron.2016.11.044
Jiang ZS, Zhang JR (2018) LncRNA SNHG5 enhances astrocytes and microglia viability via upregulating KLF4 in spinal cord injury. Int J Biol Macromol 120(Pt A):66–72. https://doi.org/10.1016/j.ijbiomac.2018.08.002
Shi Z, Pan B, Feng S (2018) The emerging role of long non-coding RNA in spinal cord injury. J Cell Mol Med 22(4):2055–2061. https://doi.org/10.1111/jcmm.13515
Wang S, Smith GM, Selzer ME, Li S (2019) Emerging molecular therapeutic targets for spinal cord injury. Expert Opin Ther Targets 23(9):787–803. https://doi.org/10.1080/14728222.2019.1661381
Khorkova O, Wahlestedt C (2017) Oligonucleotide therapies for disorders of the nervous system. Nat Biotechnol 35(3):249–263. https://doi.org/10.1038/nbt.3784
Herman PE, Bloom O (2018) Altered leukocyte gene expression after traumatic spinal cord injury: clinical implications. Neural Regen Res 13(9):1524–1529. https://doi.org/10.4103/1673-5374.237112
Oyinbo CA (2011) Secondary injury mechanisms in traumatic spinal cord injury: a nugget of this multiply cascade. Acta Neurobiol Exp (Wars) 71(2):281–299
Dong X, Muppani NR, Wu J (2016) Long noncoding RNAs: critical regulators for cell lineage commitment in the central nervous system. Transcriptomics and gene regulation. Springer, pp 73–97
Wang F, Liu J, Wang X, Chen J, Kong Q, Ye B, Li Z (2019) The emerging role of lncRNAs in spinal cord injury. Biomed Res Int 2019:3467121. https://doi.org/10.1155/2019/3467121
Li Z, Ho IHT, Li X, Xu D, Wu WKK, Chan MTV, Li S, Liu X (2019) Long non-coding RNAs in the spinal cord injury: novel spotlight. J Cell Mol Med 23(8):4883–4890. https://doi.org/10.1111/jcmm.14422
Herrmann JE, Imura T, Song B, Qi J, Ao Y, Nguyen TK, Korsak RA, Takeda K, Akira S, Sofroniew MV (2008) STAT3 is a critical regulator of astrogliosis and scar formation after spinal cord injury. J Neurosci 28(28):7231–7243. https://doi.org/10.1523/JNEUROSCI.1709-08.2008
Gong L, Lv Y, Li S, Feng T, Zhou Y, Sun Y, Mi D (2020) Changes in transcriptome profiling during the acute/subacute phases of contusional spinal cord injury in rats. Ann Transl Med 8(24):1682. https://doi.org/10.21037/atm-20-6519
Milich LM, Choi JS, Ryan C, Cerqueira SR, Benavides S, Yahn SL, Tsoulfas P, Lee JK (2021) Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord. J Exp Med. https://doi.org/10.1084/jem.20210040
Llorens-Bobadilla E, Chell JM, Le Merre P, Wu Y, Zamboni M, Bergenstrahle J, Stenudd M, Sopova E, Lundeberg J, Shupliakov O, Carlen M, Frisen J (2020) A latent lineage potential in resident neural stem cells enables spinal cord repair. Science. https://doi.org/10.1126/science.abb8795
Alizadeh A, Dyck SM, Karimi-Abdolrezaee S (2019) Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Front Neurol 10:282. https://doi.org/10.3389/fneur.2019.00282
Tran AP, Warren PM, Silver J (2021) New insights into glial scar formation after spinal cord injury. Cell Tissue Res. https://doi.org/10.1007/s00441-021-03477-w
da Espirito Santo CC, da Silva FF, Ilha J, Duarte M, Duarte T, Santos ARS (2019) Spinal cord injury by clip-compression induces anxiety and depression-like behaviours in female rats: the role of the inflammatory response. Brain Behav Immun 78:91–104. https://doi.org/10.1016/j.bbi.2019.01.012
Zhang T, Li K, Zhang ZL, Gao K, Lv CL (2021) LncRNA Airsci increases the inflammatory response after spinal cord injury in rats through the nuclear factor kappa B signaling pathway. Neural Regen Res 16(4):772–777. https://doi.org/10.4103/1673-5374.295335
Arumugam TV, Okun E, Tang SC, Thundyil J, Taylor SM, Woodruff TM (2009) Toll-like receptors in ischemia-reperfusion injury. Shock 32(1):4–16. https://doi.org/10.1097/SHK.0b013e318193e333
Li XQ, Wang J, Fang B, Tan WF, Ma H (2014) Intrathecal antagonism of microglial TLR4 reduces inflammatory damage to blood-spinal cord barrier following ischemia/reperfusion injury in rats. Mol Brain 7:28. https://doi.org/10.1186/1756-6606-7-28
Jia H, Ma H, Li Z, Chen F, Fang B, Cao X, Chang Y, Qiang Z (2019) Downregulation of LncRNA TUG1 inhibited TLR4 signaling pathway-mediated inflammatory damage after spinal cord ischemia reperfusion in rats via suppressing TRIL expression. J Neuropathol Exp Neurol 78(3):268–282. https://doi.org/10.1093/jnen/nly126
Li JW, Kuang Y, Chen L, Wang JF (2018) LncRNA ZNF667-AS1 inhibits inflammatory response and promotes recovery of spinal cord injury via suppressing JAK-STAT pathway. Eur Rev Med Pharmacol Sci 22(22):7614–7620. https://doi.org/10.26355/eurrev_201811_16375
Orr MB, Gensel JC (2018) Spinal cord injury scarring and inflammation: therapies targeting glial and inflammatory responses. Neurotherapeutics 15(3):541–553. https://doi.org/10.1007/s13311-018-0631-6
O’Shea TM, Burda JE, Sofroniew MV (2017) Cell biology of spinal cord injury and repair. J Clin Invest 127(9):3259–3270. https://doi.org/10.1172/JCI90608
Li Y, He X, Kawaguchi R, Zhang Y, Wang Q, Monavarfeshani A, Yang Z, Chen B, Shi Z, Meng H, Zhou S, Zhu J, Jacobi A, Swarup V, Popovich PG, Geschwind DH, He Z (2020) Microglia-organized scar-free spinal cord repair in neonatal mice. Nature 587(7835):613–618. https://doi.org/10.1038/s41586-020-2795-6
Zhou HJ, Wang LQ, Wang DB, Yu JB, Zhu Y, Xu QS, Zheng XJ, Zhan RY (2018) Long noncoding RNA MALAT1 contributes to inflammatory response of microglia following spinal cord injury via the modulation of a miR-199b/IKKbeta/NF-kappaB signaling pathway. Am J Physiol Cell Physiol 315(1):C52–C61. https://doi.org/10.1152/ajpcell.00278.2017
Zhu Y, Lyapichev K, Lee DH, Motti D, Ferraro NM, Zhang Y, Yahn S, Soderblom C, Zha J, Bethea JR, Spiller KL, Lemmon VP, Lee JK (2017) Macrophage transcriptional profile identifies lipid catabolic pathways that can be therapeutically targeted after spinal cord injury. J Neurosci 37(9):2362–2376. https://doi.org/10.1523/JNEUROSCI.2751-16.2017
Zhou J, Li Z, Wu T, Zhao Q, Zhao Q, Cao Y (2020) LncGBP9/miR-34a axis drives macrophages toward a phenotype conducive for spinal cord injury repair via STAT1/STAT6 and SOCS3. J Neuroinflammation 17(1):134. https://doi.org/10.1186/s12974-020-01805-5
Wahane S, Sofroniew MV (2021) Review article for CTR special issue edited by C. Schachtrup Title of Special Issue: “modulating scar formation for improving brain repair” Loss-of-function manipulations to identify roles of diverse glia and stromal cells during CNS scar formation. Cell Tissue Res. https://doi.org/10.1007/s00441-021-03487-8
Anderson MA, Burda JE, Ren Y, Ao Y, O’Shea TM, Kawaguchi R, Coppola G, Khakh BS, Deming TJ, Sofroniew MV (2016) Astrocyte scar formation aids central nervous system axon regeneration. Nature 532(7598):195–200. https://doi.org/10.1038/nature17623
Anderson MA, O’Shea TM, Burda JE, Ao Y, Barlatey SL, Bernstein AM, Kim JH, James ND, Rogers A, Kato B, Wollenberg AL, Kawaguchi R, Coppola G, Wang C, Deming TJ, He Z, Courtine G, Sofroniew MV (2018) Required growth facilitators propel axon regeneration across complete spinal cord injury. Nature 561(7723):396–400. https://doi.org/10.1038/s41586-018-0467-6
Wanner IB, Anderson MA, Song B, Levine J, Fernandez A, Gray-Thompson Z, Ao Y, Sofroniew MV (2013) Glial scar borders are formed by newly proliferated, elongated astrocytes that interact to corral inflammatory and fibrotic cells via STAT3-dependent mechanisms after spinal cord injury. J Neurosci 33(31):12870–12886. https://doi.org/10.1523/JNEUROSCI.2121-13.2013
Wang J, Hu B, Cao F, Sun S, Zhang Y, Zhu Q (2015) Down regulation of lncSCIR1 after spinal cord contusion injury in rat. Brain Res 1624:314–320. https://doi.org/10.1016/j.brainres.2015.07.052
Zhang N, Yin Y, Xu SJ, Wu YP, Chen WS (2012) Inflammation and apoptosis in spinal cord injury. Indian J Med Res 135:287–296
Zhang H, Li D, Zhang Y, Li J, Ma S, Zhang J, Xiong Y, Wang W, Li N, Xia L (2018) Knockdown of lncRNA BDNF-AS suppresses neuronal cell apoptosis via downregulating miR-130b-5p target gene PRDM5 in acute spinal cord injury. RNA Biol 15(8):1071–1080. https://doi.org/10.1080/15476286.2018.1493333
Gu S, Xie R, Liu X, Shou J, Gu W, Che X (2017) Long coding RNA XIST contributes to neuronal apoptosis through the downregulation of AKT phosphorylation and is negatively regulated by miR-494 in rat spinal cord injury. Int J Mol Sci. https://doi.org/10.3390/ijms18040732
Zhang H, Wang W, Li N, Li P, Liu M, Pan J, Wang D, Li J, Xiong Y, Xia L (2018) LncRNA DGCR5 suppresses neuronal apoptosis to improve acute spinal cord injury through targeting PRDM5. Cell Cycle 17(16):1992–2000. https://doi.org/10.1080/15384101.2018.1509622
Ren XD, Wan CX, Niu YL (2019) Overexpression of lncRNA TCTN2 protects neurons from apoptosis by enhancing cell autophagy in spinal cord injury. FEBS Open Bio 9(7):1223–1231. https://doi.org/10.1002/2211-5463.12651
Liu Y, Pan L, Jiang A, Yin M (2018) Hydrogen sulfide upregulated lncRNA CasC7 to reduce neuronal cell apoptosis in spinal cord ischemia-reperfusion injury rat. Biomed Pharmacother 98:856–862. https://doi.org/10.1016/j.biopha.2017.12.079
Zhong J, Jiang L, Cheng C, Huang Z, Zhang H, Liu H, He J, Cao F, Peng J, Jiang Y, Sun X (2016) Altered expression of long non-coding RNA and mRNA in mouse cortex after traumatic brain injury. Brain Res 1646:589–600. https://doi.org/10.1016/j.brainres.2016.07.002
Ren D, Chen W, Cao K, Wang Z, Zheng P (2020) Expression profiles of long non-coding RNA and messenger RNA in human traumatic brain injury. Mol Ther Nucleic Acids 22:99–113. https://doi.org/10.1016/j.omtn.2020.08.012
Simon DW, McGeachy MJ, Bayir H, Clark RSB, Loane DJ, Kochanek PM (2017) The far-reaching scope of neuroinflammation after traumatic brain injury. Nat Rev Neurol 13(9):572. https://doi.org/10.1038/nrneurol.2017.116
Dash PK, Zhao J, Hergenroeder G, Moore AN (2010) Biomarkers for the diagnosis, prognosis, and evaluation of treatment efficacy for traumatic brain injury. Neurotherapeutics 7(1):100–114. https://doi.org/10.1016/j.nurt.2009.10.019
Cheng S, Zhang Y, Chen S, Zhou Y (2021) LncRNA HOTAIR participates in microglia activation and inflammatory factor release by regulating the ubiquitination of MYD88 in traumatic brain injury. J Mol Neurosci 71(1):169–177. https://doi.org/10.1007/s12031-020-01623-7
Liu N, Sun H, Li X, Cao W, Peng A, Dong S, Yu Z (2021) Downregulation of lncRNA KCNQ1OT1 relieves traumatic brain injury induced neurological deficits via promoting “M2” microglia polarization. Brain Res Bull 171:91–102. https://doi.org/10.1016/j.brainresbull.2021.03.004
Patel NA, Moss LD, Lee JY, Tajiri N, Acosta S, Hudson C, Parag S, Cooper DR, Borlongan CV, Bickford PC (2018) Long noncoding RNA MALAT1 in exosomes drives regenerative function and modulates inflammation-linked networks following traumatic brain injury. J Neuroinflammation 15(1):204. https://doi.org/10.1186/s12974-018-1240-3
Chen C, Zhong X, Smith DK, Tai W, Yang J, Zou Y, Wang LL, Sun J, Qin S, Zhang CL (2019) Astrocyte-specific deletion of Sox2 promotes functional recovery after traumatic brain injury. Cereb Cortex 29(1):54–69. https://doi.org/10.1093/cercor/bhx303
Khakh BS, Sofroniew MV (2015) Diversity of astrocyte functions and phenotypes in neural circuits. Nat Neurosci 18(7):942–952. https://doi.org/10.1038/nn.4043
Zhou Y, Shao A, Yao Y, Tu S, Deng Y, Zhang J (2020) Dual roles of astrocytes in plasticity and reconstruction after traumatic brain injury. Cell Commun Signal 18(1):62. https://doi.org/10.1186/s12964-020-00549-2
Yu Y, Cao F, Ran Q, Wang F (2017) Long non-coding RNA Gm4419 promotes trauma-induced astrocyte apoptosis by targeting tumor necrosis factor alpha. Biochem Biophys Res Commun 491(2):478–485. https://doi.org/10.1016/j.bbrc.2017.07.021
He B, Chen W, Zeng J, Tong W, Zheng P (2021) Long noncoding RNA NKILA transferred by astrocyte-derived extracellular vesicles protects against neuronal injury by upregulating NLRX1 through binding to mir-195 in traumatic brain injury. Aging (Albany NY) 13(6):8127–8145. https://doi.org/10.18632/aging.202618
Zhang Y, Wang J, Zhang Y, Wei J, Wu R, Cai H (2019) Overexpression of long noncoding RNA Malat1 ameliorates traumatic brain injury induced brain edema by inhibiting AQP4 and the NF-kappaB/IL-6 pathway. J Cell Biochem 120(10):17584–17592. https://doi.org/10.1002/jcb.29025
Raghupathi R (2004) Cell death mechanisms following traumatic brain injury. Brain Pathol 14(2):215–222. https://doi.org/10.1111/j.1750-3639.2004.tb00056.x
Zhang X, Chen Y, Jenkins LW, Kochanek PM, Clark RS (2005) Bench-to-bedside review: apoptosis/programmed cell death triggered by traumatic brain injury. Crit Care 9(1):66–75. https://doi.org/10.1186/cc2950
Wang CF, Zhao CC, Weng WJ, Lei J, Lin Y, Mao Q, Gao GY, Feng JF, Jiang JY (2017) Alteration in long non-coding RNA expression after traumatic brain injury in rats. J Neurotrauma 34(13):2100–2108. https://doi.org/10.1089/neu.2016.4642
Dai X, Yi M, Wang D, Chen Y, Xu X (2019) Changqin NO. 1 inhibits neuronal apoptosis via suppressing GAS5 expression in a traumatic brain injury mice model. Biol Chem 400(6):753–763. https://doi.org/10.1515/hsz-2018-0340
Sun D, Yu Z, Fang X, Liu M, Pu Y, Shao Q, Wang D, Zhao X, Huang A, Xiang Z, Zhao C, Franklin RJ, Cao L, He C (2017) LncRNA GAS5 inhibits microglial M2 polarization and exacerbates demyelination. EMBO Rep 18(10):1801–1816. https://doi.org/10.15252/embr.201643668
Yi M, Dai X, Li Q, Xu X, Chen Y, Wang D (2019) Downregulated lncRNA CRNDE contributes to the enhancement of nerve repair after traumatic brain injury in rats. Cell Cycle 18(18):2332–2343. https://doi.org/10.1080/15384101.2019.1647024
Zhong J, Jiang L, Huang Z, Zhang H, Cheng C, Liu H, He J, Wu J, Darwazeh R, Wu Y, Sun X (2017) The long non-coding RNA Neat1 is an important mediator of the therapeutic effect of bexarotene on traumatic brain injury in mice. Brain Behav Immun 65:183–194. https://doi.org/10.1016/j.bbi.2017.05.001
Salehi A, Zhang JH, Obenaus A (2017) Response of the cerebral vasculature following traumatic brain injury. J Cereb Blood Flow Metab 37(7):2320–2339. https://doi.org/10.1177/0271678X17701460
Kenney K, Amyot F, Haber M, Pronger A, Bogoslovsky T, Moore C, Diaz-Arrastia R (2016) Cerebral vascular injury in traumatic brain injury. Exp Neurol 275(Pt 3):353–366. https://doi.org/10.1016/j.expneurol.2015.05.019
Li Z, Li J, Tang N (2017) Long noncoding RNA Malat1 is a potent autophagy inducer protecting brain microvascular endothelial cells against oxygen-glucose deprivation/reoxygenation-induced injury by sponging miR-26b and upregulating ULK2 expression. Neuroscience 354:1–10. https://doi.org/10.1016/j.neuroscience.2017.04.017
Yang X, Zi XH (2019) LncRNA SNHG1 alleviates OGD induced injury in BMEC via miR-338/HIF-1alpha axis. Brain Res 1714:174–181. https://doi.org/10.1016/j.brainres.2018.11.003
Acknowledgements
The authors would like to thank Ms. Neha Tallapragada and Ms. Pooja Sashital for editing the manuscript.
Funding
This work was supported by Grants from the NIH, United States (R01 NS088353, R21 NS113068-01, and R21 EY028647-01), The Staman Ogilvie Fund-Memorial Hermann Foundation, and Mission Connect, a program of The Institute for Rehabilitation and Research (TIRR) Foundation.
Author information
Authors and Affiliations
Contributions
XW, HW, and JQW wrote the manuscript. All the authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval and consent to participate
No animal or human study was performed.
Consent for publication
All the authors gave their consent for publication.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Wu, X., Wei, H. & Wu, J.Q. Coding and long non-coding gene expression changes in the CNS traumatic injuries. Cell. Mol. Life Sci. 79, 123 (2022). https://doi.org/10.1007/s00018-021-04092-2
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00018-021-04092-2