Parkar Nihal S, Akpa Belinda S, Nitsche Ludwig C, Wedgewood Lewis E, Place Aaron T, Sverdlov Maria S, Chaga Oleg, Minshall Richard D
Department of Chemical Engineering, College of Engineering and College of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Antioxid Redox Signal. 2009 Jun;11(6):1301-12. doi: 10.1089/ars.2008.2397.
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.
囊泡形成提供了一种使细胞摄取细胞外物质以及使膜成分循环利用的方式。控制两种主要内吞途径(即小窝蛋白介导的内吞作用和网格蛋白介导的内吞作用,以及新出现的囊泡途径)的机制已成为深入研究的焦点,目的是增进我们对营养物质、激素和药物递送以及病原体机会性入侵的理解。在这篇关于内吞作用的综述中,我们广泛讨论了构成控制内吞囊泡形成(从膜上出芽、内陷和分裂)分子机制的结构蛋白和信号蛋白,同时也关注了在某些细胞类型和物种中观察到的特异性。我们还讨论了内吞作用的重要生化功能及其破坏所导致的疾病,以及内吞途径关键成分的结构及其已知的机制作用。文中讨论了内吞机制的主要成分被招募到质膜的机制,在质膜上它们相互作用诱导囊泡形成,同时还讨论了用于模拟简化版内吞作用的计算方法,希望借此阐明一些可能难以通过实验确定的囊泡形成方面的问题。最后,我们提出了几个尚未解答的问题,旨在激发对细胞生物学和内吞作用建模的进一步研究兴趣。