Anderson R G, Vasile E, Mello R J, Brown M S, Goldstein J L
Cell. 1978 Nov;15(3):919-33. doi: 10.1016/0092-8674(78)90276-3.
The coated pit-coated vesicle system has a key role in the uptake of plasma low density lipoprotein (LDL) and other receptor-bound proteins in human fibroblasts. To study the distribution of coated pits and coated vesicles in fibroblasts by immunochemical techniques at both the light and electron microscopic levels, we immunized rabbits with coat protein extracted from bovine brain-coated vesicles. The resulting anti-coat protein antibody was directed predominantly against clathrin, the 180,ooo dalton protein that constitutes the major component of coat protein. By indirect immunoperoxidase electron microscopy, the anti-coat protein antibody was observed to bind specifically to coated pits on the surface of human fibroblasts and to coated vesicles within the cell. Indirect immunofluorescence and immunoperoxidase staining techniques at the light microscopic level revealed that the coat protein was distributed in fibroblasts in two distinctive patterns: as discrete foci on or near the cell surface that were linearly aligned in association with phase-dense cellular fibers (first pattern), and as intracellular foci that were randomly arranged around the cell nucleus (second pattern). The distribution of coat protein in fibroblasts was compared with the distribution of ferritin-labeled LDL, which was studied with the use of similar electron microscopic and immunofluorescence techniques. As previously reported, electron microscopic studies revealed that the LDL-ferritin binding sites at 4 degrees C were clustered in coated pits. By immunofluorescence microscopy, the LDL-ferritin that was bound to receptors within coated pits was shown to be arranged linearly over the cell surface in a pattern that was similar to the linear arrangement of coat protein (first pattern). Considered together, the current data indicate that coated pits in human fibroblasts contain a protein analogous to clathrin, and that those coated pits which contain receptors for LDL are located over intracellular fibers most likely corresponding to stress fibers. These observationa may have relevance to the mechanisms by which the coated pit-coated vesicle system efficiently delivers recptor-bound ligands to lysosomes.
被膜小窝-被膜小泡系统在人类成纤维细胞摄取血浆低密度脂蛋白(LDL)及其他受体结合蛋白的过程中起关键作用。为了运用免疫化学技术在光学显微镜和电子显微镜水平研究成纤维细胞中被膜小窝和被膜小泡的分布,我们用从牛脑被膜小泡中提取的被膜蛋白免疫兔子。所产生的抗被膜蛋白抗体主要针对网格蛋白,即构成被膜蛋白主要成分的180,000道尔顿的蛋白质。通过间接免疫过氧化物酶电子显微镜观察发现,抗被膜蛋白抗体能特异性地结合人类成纤维细胞表面的被膜小窝以及细胞内的被膜小泡。光学显微镜水平的间接免疫荧光和免疫过氧化物酶染色技术显示,被膜蛋白在成纤维细胞中有两种不同的分布模式:一种是在细胞表面或其附近呈离散的焦点,与相位密集的细胞纤维呈线性排列(第一种模式);另一种是在细胞核周围随机排列的细胞内焦点(第二种模式)。将成纤维细胞中被膜蛋白的分布与铁蛋白标记的LDL的分布进行了比较,后者是使用类似的电子显微镜和免疫荧光技术进行研究的。如先前报道,电子显微镜研究显示,4℃时LDL-铁蛋白结合位点聚集在被膜小窝中。通过免疫荧光显微镜观察,结合在被膜小窝内受体上的LDL-铁蛋白在细胞表面呈线性排列,其模式与被膜蛋白的线性排列(第一种模式)相似。综合来看,目前的数据表明,人类成纤维细胞中的被膜小窝含有一种类似于网格蛋白的蛋白质,并且那些含有LDL受体的被膜小窝位于最有可能对应于应力纤维的细胞内纤维之上。这些观察结果可能与被膜小窝-被膜小泡系统有效地将受体结合配体递送至溶酶体的机制有关。