Vesicle Formation and Endocytosis: Function, Machinery, Mechanisms, and Modeling

被引:0
|
作者
Parkar, Nihal S. [1 ,4 ]
Akpa, Belinda S. [1 ,4 ]
Nitsche, Ludwig C. [1 ,4 ]
Wedgewood, Lewis E. [1 ,4 ]
Place, Aaron T. [2 ,5 ]
Sverdlov, Maria S. [2 ,5 ]
Chaga, Oleg [2 ,5 ]
Minshall, Richard D. [2 ,3 ,5 ,6 ]
机构
[1] Univ Illinois, Dept Chem Engn, Coll Engn, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Pharmacol, Coll Engn, Chicago, IL 60612 USA
[3] Univ Illinois, Dept Anesthesiol, Coll Engn, Chicago, IL 60612 USA
[4] Univ Illinois, Coll Med, Dept Chem Engn, Chicago, IL 60612 USA
[5] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60612 USA
[6] Univ Illinois, Coll Med, Dept Anesthesiol, Chicago, IL 60612 USA
关键词
CLATHRIN-INDEPENDENT ENDOCYTOSIS; PLASMA-MEMBRANE; CAVEOLAE FORMATION; ENDOTHELIAL-CELLS; MULTIPLE STAGES; COATED PITS; LIGHT-CHAIN; PROTEIN; DYNAMIN; ACTIN;
D O I
10.1089/ars.2008.2397
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vesicle formation provides a means of cellular entry for extracellular substances and for recycling of membrane constituents. Mechanisms governing the two primary endocytic pathways (i.e., caveolae-and clathrin-mediated endocytosis, as well as newly emerging vesicular pathways) have become the focus of intense investigation to improve our understanding of nutrient, hormone, and drug delivery, as well as opportunistic invasion of pathogens. In this review of endocytosis, we broadly discuss the structural and signaling proteins that compose the molecular machinery governing endocytic vesicle formation (budding, invagination, and fission from the membrane), with some regard for the specificity observed in certain cell types and species. Important biochemical functions of endocytosis and diseases caused by their disruption also are discussed, along with the structures of key components of endocytic pathways and their known mechanistic contributions. The mechanisms by which principal components of the endocytic machinery are recruited to the plasma membrane, where they interact to induce vesicle formation, are discussed, together with computational approaches used to simulate simplified versions of endocytosis with the hope of clarifying aspects of vesicle formation that may be difficult to determine experimentally. Finally, we pose several unanswered questions intended to stimulate further research interest in the cell biology and modeling of endocytosis. Antioxid. Redox Signal. 11, 1301-1312.
引用
收藏
页码:1301 / 1312
页数:12
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