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细胞脱离触发p38丝裂原活化蛋白激酶依赖性Fas配体的过表达。肠道上皮细胞失巢凋亡的一种新机制。

Cell detachment triggers p38 mitogen-activated protein kinase-dependent overexpression of Fas ligand. A novel mechanism of Anoikis of intestinal epithelial cells.

作者信息

Rosen Kirill, Shi Wen, Calabretta Bruno, Filmus Jorge

机构信息

Sunnybrook and Women's College Health Sciences Centre, and Department of Medical Biophysics, University of Toronto, Toronto, Ontario M4N 3M5, Canada.

出版信息

J Biol Chem. 2002 Nov 29;277(48):46123-30. doi: 10.1074/jbc.M207883200. Epub 2002 Sep 27.

Abstract

Many cell types undergo apoptosis when they are detached from the extracellular matrix (ECM). This phenomenon has been termed anoikis. Most epithelial cells, which are normally attached to a type of ECM called basement membrane, are particularly sensitive to anoikis. Conversely, carcinoma cells tend to be resistant to anoikis, and this resistance plays a critical role in tumor invasion and metastasis. We reported previously that detachment-induced down-regulation of the anti-apoptotic molecule Bcl-X(L) makes a significant contribution to anoikis of intestinal epithelial cells. Here we demonstrate that exogenous Bcl-X(L), no matter how highly expressed in these cells, can significantly attenuate anoikis but cannot completely prevent it, suggesting that at least another pro-apoptotic event is activated by the loss of cell-ECM contacts. Indeed, in this study we identified a novel mechanism of anoikis in intestinal epithelial cells that involves detachment-induced overexpression of Fas ligand. We also demonstrated that this elevation in Fas ligand expression requires a detachment-induced increase of p38 mitogen-activated protein kinase activity. We conclude that the activation of at least two different pro-apoptotic events is required for anoikis of intestinal epithelial cells.

摘要

许多细胞类型在脱离细胞外基质(ECM)时会发生凋亡。这种现象被称为失巢凋亡。大多数上皮细胞通常附着于一种称为基底膜的细胞外基质类型,它们对失巢凋亡尤为敏感。相反,癌细胞往往对失巢凋亡具有抗性,并且这种抗性在肿瘤侵袭和转移中起着关键作用。我们之前报道过,脱离诱导的抗凋亡分子Bcl-X(L)的下调对肠上皮细胞的失巢凋亡有显著贡献。在此我们证明,外源性Bcl-X(L),无论在这些细胞中表达多高,都能显著减轻失巢凋亡,但不能完全阻止它,这表明细胞与细胞外基质接触的丧失至少激活了另一个促凋亡事件。事实上,在本研究中我们确定了肠上皮细胞失巢凋亡的一种新机制,该机制涉及脱离诱导的Fas配体过表达。我们还证明,Fas配体表达的这种升高需要脱离诱导的p38丝裂原活化蛋白激酶活性增加。我们得出结论,肠上皮细胞的失巢凋亡需要至少两种不同促凋亡事件的激活。

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