凋亡抑制蛋白在细胞凋亡中的调节作用

被引:3
作者
张韡
机构
[1] 上海第二医科大学附属瑞金医院传染科上海
关键词
细胞凋亡; 凋亡抑制蛋白; Caspase蛋白酶;
D O I
暂无
中图分类号
R329 [人体组织学];
学科分类号
100107 [人体解剖与组织胚胎学(人体解剖学、组织与胚胎学)];
摘要
凋亡抑制蛋白(IAP)家族是至今发现的惟一一种内源性Caspase蛋白酶抑制剂,在细胞凋亡中发挥重要的调节作用。本文结合近年来的研究进展,综述了Caspase在凋亡中的作用、IAP家族蛋白分子的结构特征、抗凋亡作用机制以及IAPs抗凋亡作用的负调控。进一步认识细胞凋亡中复杂的调控机制,为寻找与凋亡紊乱相关的疾病治疗提供了重要靶向。
引用
收藏
页码:83 / 86
页数:4
相关论文
共 9 条
[1]
Mechanisms of caspase activation and inhibition during apoptosis [J].
Shi, YG .
MOLECULAR CELL, 2002, 9 (03) :459-470
[2]
The damage-responsive Drosophila gene sickle encodes a novel IAP binding protein similar to but distinct from reaper, grim, and hid [J].
Christich, A ;
Kauppila, S ;
Chen, P ;
Sogame, N ;
Ho, SI ;
Abrams, JM .
CURRENT BIOLOGY, 2002, 12 (02) :137-140
[3]
sickle, a novel Drosophila death gene in the reaper/hid/grim region, encodes an IAP-inhibitory protein [J].
Srinivasula, SM ;
Datta, P ;
Kobayashi, M ;
Wu, JW ;
Fujioka, M ;
Hegde, R ;
Zhang, ZJ ;
Mukattash, R ;
Fernandes-Alnemri, T ;
Shi, YG ;
Jaynes, JB ;
Alnemri, ES .
CURRENT BIOLOGY, 2002, 12 (02) :125-130
[4]
Cell death regulation by the mammalian IAP antagonist Diablo/Smac [J].
Verhagen, AM ;
Vaux, DL .
APOPTOSIS, 2002, 7 (02) :163-166
[5]
The molecular basis and potential role of survivin in cancer diagnosis and therapy [J].
Altieri, DC .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (12) :542-547
[6]
Structural analysis of a functional DIAP1 fragment bound to grim and hid peptides [J].
Wu, JW ;
Cocina, AE ;
Chai, JJ ;
Hay, BA ;
Shi, YG .
MOLECULAR CELL, 2001, 8 (01) :95-104
[7]
Crystal structure and mutagenic analysis of the inhibitor-of-apoptosis protein survivin [J].
Muchmore, SW ;
Chen, J ;
Jakob, C ;
Zakula, D ;
Matayoshi, ED ;
Wu, W ;
Zhang, HC ;
Li, FZ ;
Ng, SC ;
Altieri, DC .
MOLECULAR CELL, 2000, 6 (01) :173-182
[8]
ML-IAP, a novel inhibitor of apoptosis that is preferentially expressed in human melanomas [J].
Vucic, D ;
Stennicke, HR ;
Pisabarro, MT ;
Salvesen, GS ;
Dixit, VM .
CURRENT BIOLOGY, 2000, 10 (21) :1359-1366
[9]
A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein [J].
Spiess, C ;
Beil, A ;
Ehrmann, M .
CELL, 1999, 97 (03) :339-347