Let-7/miR-98 regulate Fas and Fas-mediated apoptosis

被引:0
作者
S Wang
Y Tang
H Cui
X Zhao
X Luo
W Pan
X Huang
N Shen
机构
[1] Joint Molecular Rheumatology Laboratory of the Institute of Health Sciences and Shanghai Renji Hospital,
[2] Shanghai Institutes for Biological Sciences,undefined
[3] Chinese Academy of Sciences,undefined
[4] and Shanghai Jiaotong University School of Medicine,undefined
[5] Key Laboratory of Stem Cell Biology,undefined
[6] Shanghai Institutes for Biological Sciences,undefined
[7] Chinese Academy of Sciences,undefined
来源
Genes & Immunity | 2011年 / 12卷
关键词
microRNA; Fas; apoptosis; activation-induced cell death (AICD);
D O I
暂无
中图分类号
学科分类号
摘要
Fas is ubiquitously expressed on a variety of cells and triggers apoptosis, which have critical roles in the immune system. MicroRNAs (miRNAs) have been recently identified as regulators that modulate target gene expression and are involved in diverse biological processes, such as cell proliferation and apoptosis. This study was undertaken to investigate the contribution of miRNA in the regulation of Fas expression and Fas-mediated apoptosis. Bioinformatics analysis indicated that Fas was a potential target of let-7/miR-98 family. Indeed ectopic expression of let-7/miR-98 reduced, whereas knockdown of endogenous let-7/miR-98 increased the expression of Fas at both mRNA and protein levels. Let-7/miR-98 was verified to target Fas 3′ untranslated region directly by site-directed gene mutagenesis and reporter gene assay. More importantly, introduction of let-7/miR-98 could decrease the sensitivity to Fas-induced apoptosis. Furthermore, let-7/miR-98 expression was reduced in activation-induced cell death process, accompanied by increased expression of Fas. In conclusion, our study first demonstrated that let-7/miR-98 regulated Fas expression and the sensitivity of Fas-mediated apoptosis.
引用
收藏
页码:149 / 154
页数:5
相关论文
共 197 条
[1]  
Krueger A(2003)The role of CD95 in the regulation of peripheral T-cell apoptosis Immunol Rev 193 58-69
[2]  
Fas SC(2009)The many roles of FAS receptor signaling in the immune system Immunity 30 180-192
[3]  
Baumann S(2000)Death the Fas way: regulation and pathophysiology of CD95 and its ligand Pharmacol Ther 88 333-347
[4]  
Krammer PH(2002)Apoptosis in the immune system: 1. Fas-induced apoptosis in monocytes-derived human dendritic cells J Cell Mol Med 6 223-234
[5]  
Strasser A(2000)Fas and Fas ligand expressed on cells of the immune system, not on the target tissue, control induction of experimental autoimmune uveitis J Immunol 165 5480-5486
[6]  
Jost PJ(2002)Regulation of T cell apoptosis during the immune response Curr Mol Med 2 257-272
[7]  
Nagata S(1994)Expression of APO-1 (CD95), a member of the NGF/TNF receptor superfamily, in normal and neoplastic colon epithelium Int J Cancer 57 371-377
[8]  
Sharma K(1995)Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome Cell 81 935-946
[9]  
Wang RX(1995)Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity Science 268 1347-1349
[10]  
Zhang LY(2006)Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype Br J Haematol 133 124-140