Conrad P A, Smart E J, Ying Y S, Anderson R G, Bloom G S
Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235, USA.
J Cell Biol. 1995 Dec;131(6 Pt 1):1421-33. doi: 10.1083/jcb.131.6.1421.
Caveolin is a protein associated with the characteristic coats that decorate the cytoplasmic face of plasma membrane caveolae. Recently it was found that exposure of human fibroblasts to cholesterol oxidase (CO) rapidly induces caveolin to redistribute to the ER and then to the Golgi complex, and that subsequent removal of CO allows caveolin to return to the plasma membrane (Smart, E. J., Y.-S. Ying, P. A. Conrad, R. G. W. Anderson, J. Cell Biol. 1994, 127:1185-1197). We now present evidence that caveolin normally undergoes microtubule-dependent cycling between the plasma membrane and the Golgi. In cells that were treated briefly with nocodazole and then with a mixture of nocodazole plus CO, caveolin relocated from the plasma membrane to the ER and then to the ER/Golgi intermediate compartment (ERGIC), but subsequent movement to the Golgi was not observed. Even in the absence of CO, nocodazole caused caveolin to accumulate in the ERGIC. Nocodazole did not retard the movement of caveolin from the Golgi to the plasma membrane after removal of CO. Incubation of cells at 15 degrees followed by elevation of the temperature to 37 degrees caused caveolin to accumulate first in the ERGIC and then in the Golgi, before finally reestablishing its normal steady state distribution predominantly in plasma membrane caveolae. In cells released from a 15 degrees block, movement of caveolin from the Golgi to the plasma membrane was not inhibited by nocodazole. Taken together, these results imply that caveolin cycles constitutively between the plasma membrane and the Golgi by a multi-step process, one of which, ERGIC-to-Golgi transport, requires microtubules. This novel, bidirectional pathway may indicate roles for microtubules in the maintenance of caveolae, and for caveolin in shuttling fatty acids and cholesterol between the plasma membrane and the ER/Golgi system.
小窝蛋白是一种与特征性衣被相关的蛋白质,这些衣被装饰着质膜小窝的胞质面。最近发现,将人成纤维细胞暴露于胆固醇氧化酶(CO)会迅速诱导小窝蛋白重新分布到内质网,然后再到高尔基体复合体,并且随后去除CO可使小窝蛋白回到质膜(Smart, E. J., Y.-S. Ying, P. A. Conrad, R. G. W. Anderson, J. Cell Biol. 1994, 127:1185 - 1197)。我们现在提供证据表明,小窝蛋白通常在质膜和高尔基体之间进行依赖微管的循环。在用诺考达唑短暂处理然后用诺考达唑加CO的混合物处理的细胞中,小窝蛋白从质膜重新定位到内质网,然后到内质网/高尔基体中间区室(ERGIC),但未观察到随后向高尔基体的移动。即使在没有CO的情况下,诺考达唑也会导致小窝蛋白在内质网/高尔基体中间区室中积累。去除CO后,诺考达唑不会阻碍小窝蛋白从高尔基体向质膜的移动。将细胞在15摄氏度下孵育,然后将温度升高到37摄氏度,会导致小窝蛋白首先在内质网/高尔基体中间区室积累,然后在高尔基体中积累,最终才重新建立其主要位于质膜小窝中的正常稳态分布。在从15摄氏度阻滞中释放的细胞中,小窝蛋白从高尔基体向质膜的移动不受诺考达唑的抑制。综上所述,这些结果表明,小窝蛋白通过一个多步骤过程在质膜和高尔基体之间持续循环,其中之一,即内质网/高尔基体中间区室到高尔基体的运输,需要微管。这种新的双向途径可能表明微管在维持小窝中的作用,以及小窝蛋白在质膜与内质网/高尔基体系统之间穿梭脂肪酸和胆固醇中的作用。