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半胱天冬酶:仅仅是杀手吗?

Caspases: more than just killers?

作者信息

Los M, Stroh C, Jänicke R U, Engels I H, Schulze-Osthoff K

机构信息

Dept of Immunology and Cell Biology, University of Münster, D-48149, Münster, Germany.

出版信息

Trends Immunol. 2001 Jan;22(1):31-4. doi: 10.1016/s1471-4906(00)01814-7.

DOI:10.1016/s1471-4906(00)01814-7
PMID:11286689
Abstract

Proteases of the caspase family constitute the central executioners of apoptosis. Several recent observations suggest that caspases and apoptosis-regulatory molecules exert important functions beyond that of cell death, including the control of T-cell proliferation and cell-cycle progression. Here, Los and colleagues propose a model that directly connects cell suicide mechanisms to the regulation of cell-cycle progression.

摘要

半胱天冬酶家族的蛋白酶是细胞凋亡的核心执行者。最近的一些观察结果表明,半胱天冬酶和凋亡调节分子发挥着超出细胞死亡的重要功能,包括对T细胞增殖和细胞周期进程的控制。在这里,洛斯及其同事提出了一个将细胞自杀机制与细胞周期进程调节直接联系起来的模型。

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Caspases: more than just killers?半胱天冬酶:仅仅是杀手吗?
Trends Immunol. 2001 Jan;22(1):31-4. doi: 10.1016/s1471-4906(00)01814-7.
2
Siva-1 and an alternative splice form lacking the death domain, Siva-2, similarly induce apoptosis in T lymphocytes via a caspase-dependent mitochondrial pathway.Siva-1以及一种缺少死亡结构域的可变剪接形式Siva-2,同样通过一种半胱天冬酶依赖性线粒体途径在T淋巴细胞中诱导细胞凋亡。
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Zeta-associated protein of 70 kDa (ZAP-70), but not Syk, tyrosine kinase can mediate apoptosis of T cells through the Fas/Fas ligand, caspase-8 and caspase-3 pathways.70千道尔顿的ζ相关蛋白(ZAP-70)而非脾酪氨酸激酶(Syk),可通过Fas/Fas配体、半胱天冬酶-8和半胱天冬酶-3途径介导T细胞凋亡。
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Inhibition of NF-kappa B activity in human T lymphocytes induces caspase-dependent apoptosis without detectable activation of caspase-1 and -3.抑制人T淋巴细胞中的核因子-κB活性可诱导半胱天冬酶依赖性凋亡,而未检测到半胱天冬酶-1和-3的激活。
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The role of caspases in T cell development and the control of immune responses.半胱天冬酶在T细胞发育及免疫反应调控中的作用。
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Increased TNF-alpha-induced apoptosis in lymphocytes from aged humans: changes in TNF-alpha receptor expression and activation of caspases.老年人体内肿瘤坏死因子-α诱导淋巴细胞凋亡增加:肿瘤坏死因子-α受体表达的变化及半胱天冬酶的激活
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CD99 signals caspase-independent T cell death.CD99信号传导非半胱天冬酶依赖性T细胞死亡。
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FADD/MORT1 and caspase-8 are recruited to TRAIL receptors 1 and 2 and are essential for apoptosis mediated by TRAIL receptor 2.FADD/MORT1和半胱天冬酶-8被募集到肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体1和2上,并且对于由TRAIL受体2介导的细胞凋亡至关重要。
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Activation-induced cell death.激活诱导的细胞死亡
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Non-apoptotic functions of caspases in cellular proliferation and differentiation.半胱天冬酶在细胞增殖和分化中的非凋亡功能。
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