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外切酶解的分子和细胞机制。

Molecular and cellular mechanisms of ectodomain shedding.

机构信息

Division of Respiratory Diseases, Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Anat Rec (Hoboken). 2010 Jun;293(6):925-37. doi: 10.1002/ar.20757.

Abstract

The extracellular domain of several membrane-anchored proteins is released from the cell surface as soluble proteins through a regulated proteolytic mechanism called ectodomain shedding. Cells use ectodomain shedding to actively regulate the expression and function of surface molecules, and modulate a wide variety of cellular and physiological processes. Ectodomain shedding rapidly converts membrane-associated proteins into soluble effectors and, at the same time, rapidly reduces the level of cell surface expression. For some proteins, ectodomain shedding is also a prerequisite for intramembrane proteolysis, which liberates the cytoplasmic domain of the affected molecule and associated signaling factors to regulate transcription. Ectodomain shedding is a process that is highly regulated by specific agonists, antagonists, and intracellular signaling pathways. Moreover, only about 2% of cell surface proteins are released from the surface by ectodomain shedding, indicating that cells selectively shed their protein ectodomains. This review will describe the molecular and cellular mechanisms of ectodomain shedding, and discuss its major functions in lung development and disease.

摘要

几种膜锚定蛋白的细胞外结构域通过一种称为细胞外结构域脱落的调节性蛋白水解机制从细胞表面作为可溶性蛋白释放。细胞利用细胞外结构域脱落来主动调节表面分子的表达和功能,并调节多种细胞和生理过程。细胞外结构域脱落将膜相关蛋白迅速转化为可溶性效应物,同时迅速降低细胞表面表达水平。对于某些蛋白质,细胞外结构域脱落也是跨膜蛋白水解的前提条件,它将受影响分子的细胞质结构域和相关信号因子释放出来以调节转录。细胞外结构域脱落是一个受到特定激动剂、拮抗剂和细胞内信号通路高度调控的过程。此外,只有大约 2%的细胞表面蛋白通过细胞外结构域脱落从表面释放,表明细胞选择性地脱落其蛋白细胞外结构域。本文将描述细胞外结构域脱落的分子和细胞机制,并讨论其在肺发育和疾病中的主要功能。

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