网格蛋白依赖性内吞途径的限制和挫折。

Pub Date : 2022-12-08 DOI:10.5802/crbiol.88
Julie Bruna-Gauchoux, Guillaume Montagnac
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引用次数: 0

摘要

网格蛋白依赖性内吞作用是大多数表面受体及其配体进入的主要途径。它是由网格蛋白包裹的结构控制的,这些结构具有聚集受体和局部弯曲质膜的能力,导致含有受体的小泡的形成,出芽进入细胞质。网格蛋白包被结构的这种典型作用已被反复证明在细胞生理学的广泛方面起着基本作用。然而,现在已经清楚地确定,网格蛋白涂层结构弯曲膜的能力可能会被破坏。除了化学或遗传改变外,许多环境条件可以物理地阻止或减缓膜变形和/或网格蛋白包覆结构的出芽。由此导致的内吞作用受挫不仅是一个被动的结果,而且具有非常特殊和重要的细胞功能。在描述其原因和许多功能后果之前,我们提供了一个历史视角以及网格蛋白途径中受挫内吞作用的定义。
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Constraints and frustration in the clathrin-dependent endocytosis pathway.

Clathrin-dependent endocytosis is the major pathway for the entry of most surface receptors and their ligands. It is controlled by clathrin-coated structures that are endowed with the ability to cluster receptors and locally bend the plasma membrane, leading to the formation of receptor-containing vesicles budding into the cytoplasm. This canonical role of clathrin-coated structures has been repeatedly demonstrated to play a fundamental role in a wide range of aspects of cell physiology. However, it is now clearly established that the ability of clathrin-coated structures to bend the membrane can be disrupted. In addition to chemical or genetic alterations, many environmental conditions can physically prevent or slow membrane deformation and/or budding of clathrin-coated structures. The resulting frustrated endocytosis is not only a passive consequence but serves very specific and important cellular functions. Here we provide a historical perspective as well as a definition of frustrated endocytosis in the clathrin pathway before describing its causes and many functional consequences.

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