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肌肉特异性microRNA-206:研究现状及前景 被引量:4

Muscle-specific microRNA-206: research status and prospects
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摘要 背景:骨骼肌占了人体总体质量的40%,然而许多骨骼肌损伤和疾病的机制问题尚未解决。MicroRNA-206(miR-206)是骨骼肌特异性miRNA,在骨骼肌的发育和再生中起着重要的作用。目的:总结分析microRNA-206在骨骼肌损伤和疾病中的研究现状。方法:以"miR-206,skeletal muscle"为检索词,计算机检索1992至2014年PubMed数据库相关文献的全文,经过筛选最终对60篇miR-206在骨骼肌损伤和疾病中的相关研究进行分析讨论。结果与结论:MiR-206能调节神经肌肉损伤后神经肌肉接点的恢复。相关研究显示,控制miR-206水平可能成为治疗肌萎缩侧索硬化症等肌肉疾病的新方法。通过细胞培养发现miR-206能促进卫星细胞的分化,缺乏miR-206会导致卫星细胞延迟分化,在骨骼肌损伤中也发现mi R-206能促进骨骼肌的再生。miR-206长期运动适应后水平下降,但当运动适应停训一段时间后,miR-206会恢复到原先的水平,而其机制还有待研究。 BACKGROUND:Skeletal muscle accounts for 40%of total body weight, but mechanisms of many skeletal muscle injuries and diseases have not been resolved. MicroRNA-206 (miR-206) is a skeletal muscle-specific microRNA, which plays an important role in skeletal muscle development and regeneration. OBJECTIVE:To analyze the research status of miR-206 in skeletal muscle injuries and diseases. METHODS:A computer-based search of PubMed was performed for articles about microRNA-206 in skeletal muscle injuries and diseases published from 1992 to 2014 using the keywords of“miR-206, skeletal muscle”. Final y, 57 articles were included in result analysis. RESULTS AND CONCLUSION:miR-206 can regulate neuromuscular junction recovery after nerve muscle injury. Studies have shown that to control miR-206 levels may be a new method for the treatment of amyotrophic lateral sclerosis and other muscle diseases. miR-206 can promote the differentiation of satel ite cel s in cel culture, and the lack of miR-206 can delay the differentiation of satel ite cel s. miR-206 is also found to promote the regeneration of skeletal muscle. After long-term exercise, the miR-206 level shows an adaptive decrease, but if the exercise is stopped for some time, the miR-206 level can return to its original level. Its mechanism remains to be studied.
机构地区 上海体育学院
出处 《中国组织工程研究》 CAS 北大核心 2015年第7期1087-1093,共7页 Chinese Journal of Tissue Engineering Research
基金 国家自然科学基金项目(31171139) 上海体育学院研究生教育创新基金(yjscx2014038) 教育部上海市人类运动能力开发与保障重点实验室(上海体育学院)(11DZ2261100)~~
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  • 1Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004;116(2):281-297.
  • 2Lee RC, Feinbaum RL, Ambros V, et al. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell.1993;75(5):843-854.
  • 3Wightman B, Ha I, Ruvkun G. Posttranscriptional regulation of the heterochronic gene Iin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell. 1993;75(5):855-862.
  • 4Kozomara A, Griffiths-Jones S. miRBase: integrating microRNA annotation and deep-sequencing data. Nucleic Acids Res.2011;39(Database issue): D152-D157.
  • 5Kim VN, HanJ, Siomi MC. Biogenesis of small RNAs in animals. Nat Rev Mol Cell BioI. 2009;10(2):126-139.
  • 6Fabian MR, Sonenberg N, Filipowicz W.Regulation of mRNA translation and stability by microRNAs. Annu Rev Biochem. 2010;79:351-379.
  • 7Thomas M, LiebermanJ, Lal A. Desperately seeking microRNA targets. Nat Struct Mol BioI.2010;17(10): 1169-1174.
  • 8MccarthyJ J, Esser KA. MicroRNA-1 and microRNA-133a expression are decreased during skeletal muscle hypertrophy.J Appl Physiol (1985). 2007;102(1):306-313.
  • 9MccarthyJ J, Esser KA, Andrade FH.MicroRNA-206 is overexpressed in the diaphragm but not the hindlimb muscle of mdx mouse. AmJ Physiol Cell Physiol. 2007;293(1): C451-C457.
  • 10Small E M, O'RourkeJ R, Moresi V, et al. Regulation of Pl3-kinase/Akt signaling by muscle-enriched microRNA-486. Proc Nati Acad Sci USA. 2010; 1 07(9):4218-4223.

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