Heuser J
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Cell Biol. 1989 Feb;108(2):401-11. doi: 10.1083/jcb.108.2.401.
Reducing the internal pH of cultured cells by several different protocols that block endocytosis is found to alter the structure of clathrin lattices on the inside of the plasma membrane. Lattices curve inward until they become almost spherical yet remain stubbornly attached to the membrane. Also, the lattices bloom empty "microcages" of clathrin around their edges. Correspondingly, broken-open cells bathed in acidified media demonstrate similar changes in clathrin lattices. Acidification accentuates the normal tendency of lattices to round up in vitro and also stimulates them to nucleate microcage formation from pure solutions of clathrin. On the other hand, several conditions that also inhibit endocytosis have been found to create, instead of unusually curved clathrin lattices with extraneous microcages, a preponderance of unusually flat lattices. These treatments include pH-"clamping" cells at neutrality with nigericin, swelling cells with hypotonic media, and sticking cells to the surface of a culture dish with soluble polylysine. Again, the unusually flat lattices in such cells display a tendency to round up and to nucleate clathrin microcage formation during subsequent in vitro acidification. This indicates that regardless of the initial curvature of clathrin lattices, they all display an ability to grow and increase their curvature in vitro, and this is enhanced by lowering ambient pH. Possibly, clathrin lattice growth and curvature in vivo may also be stimulated by a local drop in pH around clusters of membrane receptors.
通过几种不同的阻断内吞作用的方法降低培养细胞的胞内pH值,发现会改变质膜内侧网格蛋白晶格的结构。晶格向内弯曲,直到它们几乎变成球形,但仍顽固地附着在膜上。此外,晶格在其边缘周围形成空的网格蛋白“微笼”。相应地,浸泡在酸化培养基中的破裂细胞在网格蛋白晶格中也表现出类似的变化。酸化增强了晶格在体外变圆的正常趋势,还刺激它们从纯网格蛋白溶液中形成微笼核。另一方面,已发现几种同样抑制内吞作用的条件,会产生大量异常扁平的晶格,而不是带有额外微笼的异常弯曲的网格蛋白晶格。这些处理包括用尼日利亚菌素将细胞的pH值“钳制”在中性,用低渗培养基使细胞肿胀,以及用可溶性聚赖氨酸将细胞粘附到培养皿表面。同样,这些细胞中异常扁平的晶格在随后的体外酸化过程中表现出变圆并形成网格蛋白微笼核的趋势。这表明,无论网格蛋白晶格的初始曲率如何,它们都具有在体外生长并增加其曲率的能力,而降低周围环境的pH值会增强这种能力。可能,膜受体簇周围局部pH值的下降也会刺激体内网格蛋白晶格的生长和曲率变化。