Molecular mechanisms of clathrin-independent endocytosis

被引:224
作者
Hansen, Carsten G. [1 ]
Nichols, Benjamin J. [1 ]
机构
[1] MRC, LMB, Cambridge CB2 0QH, England
基金
英国医学研究理事会;
关键词
CTBP; Caveolin; Clathrin; Dynamin; Endocytosis; Flotillin; GPI-ANCHORED PROTEINS; NITRIC-OXIDE SYNTHASE; RECEPTOR-MEDIATED ENDOCYTOSIS; PLASMA-MEMBRANE MICRODOMAINS; DEPRIVATION-RESPONSE-GENE; LINKED MENTAL-RETARDATION; TRANSCRIPT RELEASE FACTOR; LIVING CELL-MEMBRANES; COILED-COIL PROTEIN; CAVEOLAR ENDOCYTOSIS;
D O I
10.1242/jcs.033951
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
There is good evidence that, in addition to the canonical clathrin-associated endocytic machinery, mammalian cells possess multiple sets of proteins that are capable of mediating the formation of endocytic vesicles. The identity, mechanistic properties and function of these clathrin-independent endocytic pathways are currently under investigation. This Commentary briefly recounts how the field of clathrin-independent endocytosis has developed to date. It then highlights recent progress in identifying key proteins that might define alternative types of endocytosis. These proteins include CtBP (also known as BARS), flotillins (also known as reggies) and GRAF1. We argue that a combination of information about pathway-specific proteins and the ultrastructure of endocytic invaginations provides a means of beginning to classify endocytic pathways.
引用
收藏
页码:1713 / 1721
页数:9
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