Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Cell Biol Int. 2009 Dec 16;34(1):3-12. doi: 10.1042/CBI20090161.
In contrast with the observation in electron micrographs of partially empty vesicles in cells following secretion, it has been believed since the 1950s that during cell secretion, secretory vesicles completely merge at the cell plasma membrane, resulting in the diffusion of intravesicular contents to the cell exterior and the compensatory retrieval of the excess membrane by endocytosis. In the interim, a large body of work has been published arguing both for and against the complete merger of secretory vesicle membrane at the cell plasma membrane during secretion. The only definitive determination of the mechanism of cell secretion remained in its direct observation at nanometre resolution in live cells. In the past decade, this finally became a reality through the power and scope of the atomic force microscope, which has made it possible to resolve a major conundrum in cell biology. This paradigm shift in our understanding of cell secretion is briefly outlined here.
与细胞分泌后电子显微镜下观察到部分排空囊泡的观察结果形成对比的是,自 20 世纪 50 年代以来,人们一直认为在细胞分泌过程中,分泌囊泡完全融合在细胞膜上,导致囊泡内物质扩散到细胞外,多余的膜通过胞吞作用被回收。在此期间,大量的研究工作发表,对分泌过程中囊泡膜是否完全融合在细胞膜上进行了争论。确定细胞分泌机制的唯一明确方法仍然是在活细胞中以纳米分辨率直接观察。在过去的十年中,这一目标终于通过原子力显微镜的强大功能和范围得以实现,这使得解决细胞生物学中的一个重大难题成为可能。本文简要概述了我们对细胞分泌理解的这一范式转变。