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真核翻译延伸因子 1A 通过触发细胞脱离诱导细胞凋亡。

Eukaryotic translation elongation factor 1A induces anoikis by triggering cell detachment.

机构信息

Department of Molecular Pathophysiology, Tokyo University of Science, Chiba 278-8510, Japan.

出版信息

J Biol Chem. 2012 May 4;287(19):16037-46. doi: 10.1074/jbc.M111.308122. Epub 2012 Mar 7.

Abstract

Anoikis, apoptosis because of loss of cell anchorage, is crucial for tissue homeostasis. Fibronectin not only provides a scaffold for cell anchorage but also harbors a cryptic antiadhesive site capable of inducing β1-integrin inactivation. In this study, this cryptic antiadhesive site is implicated in spontaneous induction of anoikis. Nontransformed fibroblasts (NIH3T3) adhering to a fibronectin substratum underwent anoikis during serum starvation culture. This anoikis was caused by proteolytic exposure of the cryptic antiadhesive site in fibronectin by matrix metalloproteinase. Eukaryotic elongation factor 1A (eEF1A) was identified as a membrane receptor for the exposed antiadhesive site. Serum starvation raised the membrane residence of eEF1A, and siRNA-based disruption of this increase rendered cells anoikis-resistant. By contrast, cells became more susceptible to anoikis in parallel with increased membrane residence of eEF1A by enforced expression. These results demonstrate that eEF1A acts as a membrane receptor for the cryptic antiadhesive site of fibronectin, which contributes to cell regulation, including anoikis, through negative regulation of cell anchorage.

摘要

失巢凋亡是由于细胞失去锚定而发生的细胞凋亡,对组织稳态至关重要。纤连蛋白不仅为细胞锚定提供支架,还含有一个隐藏的抗黏附位点,能够诱导β1 整合素失活。在这项研究中,这个隐藏的抗黏附位点与自发诱导失巢凋亡有关。附着在纤连蛋白基质上的非转化成纤维细胞(NIH3T3)在血清饥饿培养中经历失巢凋亡。这种失巢凋亡是由基质金属蛋白酶对纤连蛋白中隐藏的抗黏附位点的蛋白水解暴露引起的。真核延伸因子 1A(eEF1A)被鉴定为暴露的抗黏附位点的膜受体。血清饥饿会增加 eEF1A 的膜驻留,而基于 siRNA 的这种增加的破坏使细胞对失巢凋亡具有抗性。相比之下,通过强制表达增加 eEF1A 的膜驻留,细胞对失巢凋亡的敏感性增加。这些结果表明,eEF1A 作为纤连蛋白隐藏的抗黏附位点的膜受体发挥作用,通过负向调节细胞锚定,参与细胞调节,包括失巢凋亡。

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