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基质脱离诱导半胱天冬酶依赖性细胞色素c从线粒体释放:受蛋白激酶B/蛋白激酶B(PKB/Akt)信号通路抑制,但不受Raf信号通路抑制。

Matrix detachment induces caspase-dependent cytochrome c release from mitochondria: inhibition by PKB/Akt but not Raf signalling.

作者信息

Rytömaa M, Lehmann K, Downward J

机构信息

Signal Transduction Laboratory, Imperial Cancer Research Fund, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.

出版信息

Oncogene. 2000 Sep 14;19(39):4461-8. doi: 10.1038/sj.onc.1203805.

Abstract

Detachment of epithelial cells from extracellular matrix results in induction of apoptosis ('anoikis') which can be blocked by expression of activated Ras or PKB/Akt. Here we show that detachment causes release of cytochrome c from mitochondria in MDCK cells. This is blocked by caspase inhibitors, suggesting a role for caspases upstream of mitochondria in the initiation of anoikis, in accord with the ability of dominant negative FADD to inhibit this form of cell death. Bulk activation of caspase-8 following detachment lags behind cytochrome c release, and is likely the result of a mitochondrial positive feed back loop. Matrix detachment also induces Bax translocation to mitochondria in a caspase-dependent manner. Expression of activated Ras or PKB/Akt blocks all the detectable events on the detachment-induced apoptosis signalling pathway, suggesting that PKB/Akt acts at an early point in the pathway, providing the signal normally generated by matrix attachment. Strong activation of Raf can also protect MDCK cells from detachment induced apoptosis, but this occurs at a point downstream of cytochrome c release from mitochondria, and is clearly distinct from the effect of PKB/Akt. Oncogene (2000) 19, 4461 - 4468.

摘要

上皮细胞与细胞外基质脱离会导致凋亡(“失巢凋亡”)的诱导,而活化的Ras或蛋白激酶B/蛋白激酶B(PKB/Akt)的表达可阻断这种凋亡。在此我们表明,脱离会导致MDCK细胞中线粒体释放细胞色素c。这被半胱天冬酶抑制剂所阻断,提示半胱天冬酶在失巢凋亡起始过程中线粒体上游发挥作用,这与显性负性FADD抑制这种细胞死亡形式的能力一致。脱离后半胱天冬酶-8的大量活化滞后于细胞色素c的释放,且可能是线粒体正反馈环的结果。基质脱离还以半胱天冬酶依赖性方式诱导Bax转位至线粒体。活化的Ras或PKB/Akt的表达阻断了失巢凋亡信号通路中所有可检测到的事件,提示PKB/Akt在该通路的早期发挥作用,提供通常由基质附着产生的信号。Raf的强烈活化也可保护MDCK细胞免受脱离诱导的凋亡,但这发生在线粒体释放细胞色素c的下游,且明显不同于PKB/Akt的作用。《癌基因》(2000年)第19卷,第4461 - 4468页

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