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由于氨基磷脂跨活细胞质膜转运而导致的内吞作用增强。

Enhancement of endocytosis due to aminophospholipid transport across the plasma membrane of living cells.

作者信息

Farge E, Ojcius D M, Subtil A, Dautry-Varsat A

机构信息

Unité de Biologie des Interactions Cellulaires, Institut Pasteur, Unité de Recherches Associée 1960, Centre National de la Recherche Scientifique, F-75724 Paris Cedex 15, France.

出版信息

Am J Physiol. 1999 Mar;276(3):C725-33. doi: 10.1152/ajpcell.1999.276.3.C725.

Abstract

Formation of intracellular vesicles is initiated by membrane budding. Here we test the hypothesis that the plasma membrane surface area asymmetry could be a driving force for vesicle formation during endocytosis. The inner layer phospholipid number was therefore increased by adding exogenous aminophospholipids to living cells, which were then translocated from the outer to the inner layer of the membrane by the ubiquitous flippase. Addition of either phosphatidylserine or phosphatidylethanolamine led to an enhancement of endocytosis, showing that the observed acceleration does not depend on the lipid polar head group. Conversely, a closely related aminophospholipid that is not recognized by the flippase, lyso-alpha-phosphatidylserine, inhibited endocytosis, and similar results were obtained with a cholesterol derivative that also remains in the plasma membrane outer layer. Thus an increase of lipid concentration in the inner layer enhanced internalization, whereas an increase of the lipid concentration in the outer layer inhibited internalization. These experiments suggest that transient asymmetries in lipid concentration might contribute to the formation of endocytic vesicles.

摘要

细胞内囊泡的形成始于膜出芽。在此,我们检验了一个假说,即质膜表面积不对称可能是内吞作用期间囊泡形成的驱动力。因此,通过向活细胞中添加外源性氨基磷脂来增加内层磷脂数量,这些氨基磷脂随后通过普遍存在的翻转酶从膜的外层转运至内层。添加磷脂酰丝氨酸或磷脂酰乙醇胺均导致内吞作用增强,表明观察到的加速并不取决于脂质极性头部基团。相反,一种不被翻转酶识别的密切相关的氨基磷脂——溶血α-磷脂酰丝氨酸,抑制了内吞作用,使用同样保留在质膜外层的胆固醇衍生物也得到了类似结果。因此,内层脂质浓度的增加增强了内化作用,而外层脂质浓度的增加则抑制了内化作用。这些实验表明,脂质浓度的瞬时不对称可能有助于内吞囊泡的形成。

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