'Tissue' transglutaminase in cell death: a downstream or a multifunctional upstream effector?

被引:166
|
作者
Melino, G
Piacentini, M
机构
[1] Univ Roma Tor Vergata, Dept Expt Med F153 D26, Ist Dermopat Immacolata, Biochem Lab,IDI,IRCCS, I-00133 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
来源
FEBS LETTERS | 1998年 / 430卷 / 1-2期
关键词
apoptosis; cell death; transglutaminase; protein cross-link; retinoblastoma protein; caspase; S-nitrosylation;
D O I
10.1016/S0014-5793(98)00521-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptotic cells show morphological modifications which occur as the result of complex molecular mechanisms involving several proteins including 'tissue' transglutaminase (tTG), Although tTG was originally thought to be responsible for the protein crosslinks which prevent the leakage of intracellular components, thereby reducing inflammation and autoimmunity, recent evidence indicates that tTG is a multifunctional enzyme involved in the complex upstream regulation of the apoptotic machinery: (i) it functions as a GTP-binding protein to transduce signals; (ii) it binds/crosslinks only specific cytosolic and nuclear substrates, suggesting highly specific actions, e,g. on intermediate filaments and in cell cycle control; (iii) it is finely tuned by Ca2+, GTP, S-nitrosylation, polyamines, In Light of these recent discoveries, the role of tTG in the regulation of the crucial balance between survival and death is clearly complex, (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:59 / 63
页数:5
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