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microRNA在自身免疫性疾病中的研究进展 被引量:2

Advances in research on microRNA in autoimmune diseases
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摘要 microRNA(简称miRNA)是一类新发现、短序列的、非编码的小分子RNA,参与基因组转录后水平的调节。当前认为miRNA可以调控30%人类编码蛋白质的基因,且一种miRNA可以和多个靶mRNA结合;miRNA在免疫细胞增殖、分化、成熟、免疫稳态的维持等方面有重要调控作用。近来研究证实异常表达的miRNA与某些疾病如肿瘤、炎症性疾病及自身免疫性疾病等发病有关。本文就当前对于miRNA生物学特性,及其与自身免疫性疾病的关系进行综述。 MicroRNAs(abbreviated miRNA)are newly discovered,small,noncoding ribonucleic acids(RNAs)that play critical roles in the regulation of host genome expression at the posttranscriptional level.It is believed that miRNAs could regulate over one third of human genes that encode proteins,one miRNA may identify or regulate multiple targets.MiRNAs have served as key regulators of various biological processes including immune cell proliferation,differentiation,maturation,and maintenance of immune homeostasis and normal function.Dysregulated miRNA expression has confirmed to be relevant to a broad range of diseases including cancer as well as inflammatory and autoimmune diseases.This review focuses on the current understanding of miRNA biogenesis,and the association of miRNAs with autoimmune diseases.
出处 《实用医院临床杂志》 2012年第3期21-25,共5页 Practical Journal of Clinical Medicine
基金 国家自然科学基金项目(编号:81072479 81170263)
关键词 MICRORNA 自身免疫性疾病 免疫系统 microRNA Autoimmune disease Immune system
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  • 1Bushati N,Cohen SM. microRNA Functions[J]. Annu Rev Cell Dev Biol,2007,23( 1 ) :175-205. 被引量:1
  • 2Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochrenic gene lin-4 encodes small RNAs with antisense complementarity to lin-14 [ J]. Cell, 1993,75 (5) :843-854. 被引量:1
  • 3Wightman B, Ha I, Ruvkun G. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans[ J]. Cell, 1993,75 (5) :855-862. 被引量:1
  • 4Pasquinelli AE, Reinbart B J, Slack F, et al. Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA [ J ]. Nature,2000,408 ( 6808 ) : 86 -89. 被引量:1
  • 5Lewis BP, Burge CB, Bartel DP. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets [ J ]. Ce11,2005,120 ( 1 ) : 15-20. 被引量:1
  • 6Cai X, Hagedorn CH, Cullcn BR. Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs[ J]. Rna,2004,10 ( 12 ) : 1957. 被引量:1
  • 7Bohnsack MT,Czaplinski K,Rlich DG. Exportin 5 is a RanGTP-dependent dsRNA-binding protein that, mediates nuclear export of premiRNAs [ J]. Rna,2004,10 (2) : 185. 被引量:1
  • 8Gregory RI, Chendrimada TP, Cooch N, et al. Human RISC couples microRNA biogenesis and posttranscriptional gene silencing [ J ]. Cell, 2005,123 ( 4 ) :631-640. 被引量:1
  • 9Saxena S, Jonsson ZO, Dutta A, et al. Small RNAs with imperfect match to endogenous mRNA repress translation [ J ]. Journal of Biological Chemistry, 2003,278 ( 45 ) :44312. 被引量:1
  • 10Humphreys DT, Westman B J, Martin DI, et al. MicroRNAs control translation initiation by inhibiting eukaryotic initiation factor 4E/cap and poly( A)tail function[ J]. Proceedings of the National Academy of Sciences of the United States of America,2005,102 (47) : 16961. 被引量:1

同被引文献17

  • 1Tiegs G,Hentshel J,Wendel A. T cell-dependentexperimental liver injury in mice induced by Con-canavalin A[J]. J Clin Invest, 1992,90(1) : 196 —203. 被引量:1
  • 2Tiegs G,Hentshel J,Wendel A. T cell-dependentexperimental liver injury in mice induced by Con-canavalin A[J]. J Clin Invest, 1992,90(1) : 196 —203. 被引量:1
  • 3Nakaya M, Hashimoto M,Nakagawa R,et al.SOCS3 in T and NKT cells negatively regulates cy-tokine production and ameliorates ConA inducedhepatitis[J], J Immunol, 2009, 183(11): 7047 —7053. 被引量:1
  • 4Meng F, Henson R, Hania WJ et al. The MicroR-NA let-7a modulates interleukin-6-dependentST AT-3 survival signaling in malignant humancholangiocytes[J]. J Biol Chem, 2007,282 ( 11 ):8256-8264. 被引量:1
  • 5Zhang Y,Wang X, Zhong M, et al. MicroRNA let-7a ameliorates con A-induced hepatitis by inhibitingIL-6-dependent Thl7 cell differentiation[J]. J ClinImmunol, 2013, 33(3): 630-639. 被引量:1
  • 6Li QJ, Chau J,Ebert PJ, et al. miR-181a is an in-trinsic modulator of T cell sensitivity and selection[J]. Cell, 2007,129(1) : 147 — 161. 被引量:1
  • 7Li QJ, Chau J,Ebert PJ, et al. miR-181a is an in-trinsic modulator of T cell sensitivity and selection[J]. Cell, 2007,129(1) : 147 — 161. 被引量:1
  • 8Lin YC, Kuo MW, Yu J et al. c-Myb is an evolu-tionary conserved miR-150 target and miR-150/c-Myb interaction is important for embryonic develop-ment[J]. Mol Biol Evol, 2008,25 (10) : 2189 —2198. 被引量:1
  • 9Xiao C, Calado DP, Galler G,et al. MiR-150 con-trols B cell differentiation by targeting the transcrip-tion factor c-Myb[J]. Cell,2007,131(1): 146 —159. 被引量:1
  • 10Schmann J, Wolf D, Pahl A, et al. Importanceof Kupffer cells for T-cell-dependent liver injury inmice[J]. Am J Pathol, 2000,157 (5): 16711683. 被引量:1

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