Angiogenin inhibits nuclear translocation of apoptosis inducing factor in a Bcl-2-dependent manner

被引:21
作者
Li, Shuping [1 ,2 ]
Yu, Wenhao [1 ]
Hu, Guo-Fu [1 ,3 ]
机构
[1] Tufts Med Ctr, Mol Oncol Res Inst, Boston, MA 02111 USA
[2] Zhejiang Univ, Coll Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[3] Tufts Univ, Sackler Sch Grad Biomed Sci, Grad Program Biochem, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; MOUSE MODEL; TRANSFER-RNA; POLY(ADP-RIBOSE) POLYMERASE; NEURONAL CULTURES; FACTOR AIF; STRESS; ALS; EXPRESSION; CASPASE-1;
D O I
10.1002/jcp.22881
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Loss-of-function mutations in angiogenin (ANG) gene were discovered in amyotrophic lateral sclerosis (ALS) patients and ANG has been shown to prevent neuronal death both in vitro and in vivo. The neuro-protective activity of ANG was brought about partially by inhibiting stress-induced apoptosis. ANG attenuates both the extrinsic and the intrinsic apoptotic signals by activating Nf-?b-mediated cell survival pathway and Bcl-2-mediated anti-apoptotic pathway. Here we report that ANG inhibits nuclear translocation of apoptosis inducing factor (AIF), an important cell death-executing molecule known to play a dominant role in neurodegenerative diseases. ANG inhibits serum withdrawal-induced apoptosis by attenuating a series of Bcl-2-dependent events including caspase-3 activation, poly ADP-ribose polymerase-1 (PARP-1) cleavage, and AIF nuclear translocation. J. Cell. Physiol. 227: 1639-1644, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:1639 / 1644
页数:6
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