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半胱天冬酶-11参与TPEN诱导的细胞凋亡。

The involvement of caspase-11 in TPEN-induced apoptosis.

作者信息

Lee Jong-Min, Kim Yu-Jin, Ra Hana, Kang Shin-Jung, Han Seungjin, Koh Jae-Young, Kim Yang-Hee

机构信息

Department of Molecular Biology, Sejong University, 98 Gunja-Dong Gwangjin-Gu, Seoul 143-747, South Korea.

出版信息

FEBS Lett. 2008 Jun 11;582(13):1871-6. doi: 10.1016/j.febslet.2008.04.056. Epub 2008 May 12.

Abstract

The depletion of intracellular zinc with N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) induces protein synthesis-dependent apoptosis. Here we examined the involvement of caspase induction in apoptosis. Among the examined caspases, only caspase-11 was increased by TPEN. Caspase-11 activity also increased, which resulted in caspase-3 activation. Cycloheximide or actinomycin D blocked caspase-11 induction, reduced caspase-11 and -3 activation, and attenuated TPEN-induced neuronal apoptosis. Blockade of caspase-11 by a chemical inhibitor or genetic deletion attenuated TPEN-induced apoptosis, indicating a critical role of caspase-11 in TPEN-induced apoptosis. Although mitochondria-mediated caspase-9/-3 activation also contributed to TPEN-induced apoptosis, caspase-11 is likely a key inducible apoptosis-inducing protein.

摘要

用N,N,N',N'-四(2-吡啶甲基)乙二胺(TPEN)耗尽细胞内锌会诱导蛋白质合成依赖性凋亡。在此,我们研究了半胱天冬酶诱导在凋亡中的作用。在所检测的半胱天冬酶中,只有半胱天冬酶-11被TPEN上调。半胱天冬酶-11的活性也增加,导致半胱天冬酶-3活化。放线菌酮或放线菌素D阻断半胱天冬酶-11的诱导,降低半胱天冬酶-11和-3的活化,并减轻TPEN诱导的神经元凋亡。化学抑制剂或基因缺失对半胱天冬酶-11的阻断减轻了TPEN诱导的凋亡,表明半胱天冬酶-11在TPEN诱导的凋亡中起关键作用。虽然线粒体介导的半胱天冬酶-9/-3活化也促成了TPEN诱导的凋亡,但半胱天冬酶-11可能是关键的可诱导凋亡蛋白。

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