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miRNAs与脊髓损伤后小胶质细胞的交互作用

Cross-talk between miRNAs and microglia after spinal cord injury
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摘要 脊髓损伤(spinal cord injury,SCI)是一类主要由外力引起脊柱骨折或脱位而导致的脊髓损坏,其进展过程主要分为原发性损伤和继发性损伤两个阶段。在继发性损伤阶段,小胶质细胞对疾病发展和转归起着重要作用,其通过自身活化、诱发炎症反应、改变自身极化状态来调节中枢损伤微环境。miRNAs是一类微小非编码RNA,其主要通过靶向调控下游基因来发挥生物学效能,从而参与脊髓损伤的病理发展。miRNA与小胶质细胞的交互作用对促进脊髓损伤后中枢神经系统修复有重要意义。本文就脊髓损伤后miRNAs对小胶质细胞的影响进行综述。 Spinal cord injury(SCI)is a spinal damage mainly caused by spinal fracture or dislocation which induced by external force.Its progression process is mainly divided into two stages:primary injury and secondary injury.During secondary injury,microglia play an important role in the development and prognosis of disease.They regulate the microenvironment of central injury through self-activation,inducing inflammatory response and microglial polarization.miRNAs are a kind of micro noncoding RNAs,which play a biological role mainly through targeting and regulating downstream genes,participating in the pathological development of SCI.The cross-talk between miRNA and microglia is of great significance to promote the repair of central nervous system after spinal cord injury.In this article,we reviewed the effect of miRNAs on microglia after spinal cord injury to provide some ideas for clinical diagnosis and treatment.
作者 常星宇 鲁玉宝 陈雅杰 何咏霖 朱国贸 余晶 王学习 Chang Xingyu;Lu Yubao;Chen Yajie;He Yonglin;Zhu Guomao;Yu Jing;Wang Xuexi(The First Clinical Medical College,Lanzhou University,Lanzhou 730000,China;Spine Surgery of the Third Affiliated Hospital of Sun Yat-Sen University,Guangzhou 510635,China;Institute of integrated traditional Chinese and Western Medicine,School of Basic Medical Sciences,Lanzhou University,Lanzhou 730000,China)
出处 《中国组织化学与细胞化学杂志》 CAS CSCD 2022年第1期79-84,共6页 Chinese Journal of Histochemistry and Cytochemistry
基金 兰州市人才创新创业项目(2020-RC-40) 兰州市城关区科技计划项目(2021-9-6) 兰州大学“莙政基金”科研见习进修项目(LZU-JZH2424) 甘肃省科技计划项目(21JR7RA445) 兰州大学2020年大学生创新创业及卓越计划(20200060103)。
关键词 脊髓损伤 MIRNA 小胶质细胞 Spinal cord injury miRNA microglia
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  • 1Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell 2009; 136:215–233. | Article | PubMed | ISI | CAS |.
  • 2Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 2004; 116:281–297. | Article | PubMed | ISI | CAS |.
  • 3Filipowicz W, Bhattacharyya SN, Sonenberg N. Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? Nat Rev Genet 2008; 9:102–114. | Article | PubMed | ISI | CAS |.
  • 4Nilsen TW. Mechanisms of microRNA-mediated gene regulation in animal cells. Trends Genet 2007; 23:243–249. | Article | PubMed | ISI | CAS |.
  • 5Guo H, Ingolia NT, Weissman JS, Bartel DP. Mammalian microRNAs predominantly act to decrease target mRNA levels. Nature 2010; 466:835–840. | Article | PubMed | ISI | CAS |.
  • 6Coller J, Parker R. Eukaryotic mRNA decapping. Annu Rev Biochem 2004; 73:861–890. | Article | PubMed | ISI | CAS |.
  • 7Djuranovic S, Nahvi A, Green R. miRNA-mediated gene silencing by translational repression followed by mRNA deadenylation and decay. Science 2012; 336:237–240. | Article | PubMed | CAS |.
  • 8Bazzini AA, Lee MT, Giraldez AJ. Ribosome profiling shows that miR-430 reduces translation before causing mRNA decay in zebrafish. Science 2012; 336:233–237. | Article | PubMed | CAS |.
  • 9Huntzinger E, Izaurralde E. Gene silencing by microRNAs: contributions of translational repression and mRNA decay. Nat Rev Genet 2011; 12:99–110. | Article | PubMed | ISI | CAS |.
  • 10Coller J, Parker R. General translational repression by activators of mRNA decapping. Cell 2005; 122:875–886. | Article | PubMed | ISI | CAS |.

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