Goldberg R I, Smith R M, Jarett L
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
J Cell Physiol. 1987 Nov;133(2):203-12. doi: 10.1002/jcp.1041330202.
This ultrastructural study compared the endocytosis of a peptide hormone, ferritin-labeled insulin (Fm-I) or gold-labeled insulin (Au-I), and a non-hormonal ligand, gold-labeled alpha-2-macroglobulin-methylamine (Au-alpha 2MGMA), by rat adipocytes. Quantitative analysis of the cell surface showed that coated pits occupied 0.4% of the adipocyte surface. This was one fifth to one tenth of that which has been reported on fibroblasts and hepatocytes, cell types in which receptor-mediated endocytosis has been extensively studied. In contrast, uncoated micropinocytotic invaginations were quite numerous and occupied 13.1% of the adipocyte cell surface. The frequency of micropinocytotic invaginations, 13.8 per micron 2 of plasma membrane, was 7-12 times greater than has been reported on fibroblasts. Therefore, the ultrastructure of the endocytic apparatus on rat adipocytes was different from more commonly studied cell types. At 4 degrees C, Au-alpha 2MGMA concentrated within coated pits to a density that was 52 times greater than that on the uncoated plasma membrane. Au-alpha 2MGMA was excluded from micropinocytotic invaginations by more than 93%; this exclusion was unrelated to the size of the Au-alpha 2MGMA particle. In contrast, at 4 degrees C, Fm-I did not concentrate within coated pits and occupied micropinocytotic invaginations in a random manner. At 37 degrees C, coated pits accounted for all of the endocytosis of Au-alpha 2MGMA, proving that these structures were functional despite their atypically low density. In contrast, greater than 99% of the endocytosis of Fm-I or Au-I occurred through micropinocytotic invaginations. These results demonstrated for the first time by a comparative, quantitative, ultrastructural method that insulin and Au-alpha 2MGMA undergo endocytosis by dissimilar mechanisms on rat adipocytes. Dissimilarities in the endocytosis of insulin and Au-alpha 2MGMA may be related to the different biological roles of these two molecules.
这项超微结构研究比较了大鼠脂肪细胞对一种肽类激素、铁蛋白标记的胰岛素(Fm-I)或金标记的胰岛素(Au-I),以及一种非激素配体、金标记的α-2-巨球蛋白-甲胺(Au-α2MGMA)的内吞作用。对细胞表面的定量分析表明,有被小窝占脂肪细胞表面的0.4%。这是在成纤维细胞和肝细胞中所报道比例的五分之一到十分之一,而成纤维细胞和肝细胞是受体介导的内吞作用已被广泛研究的细胞类型。相比之下,未被包被的微胞饮内陷相当多,占脂肪细胞表面的13.1%。微胞饮内陷的频率为每平方微米质膜13.8个,比在成纤维细胞中所报道的频率高7至12倍。因此,大鼠脂肪细胞内吞装置的超微结构不同于更常被研究的细胞类型。在4℃时,Au-α2MGMA在有被小窝内浓缩,其密度比未被包被的质膜上的密度高52倍。Au-α2MGMA被排除在微胞饮内陷之外达93%以上;这种排除与Au-α2MGMA颗粒的大小无关。相比之下,在4℃时,Fm-I没有在有被小窝内浓缩,而是随机占据微胞饮内陷。在37℃时,有被小窝介导了Au-α2MGMA的所有内吞作用,证明这些结构尽管其密度异常低但仍具有功能。相比之下,Fm-I或Au-I的内吞作用中超过99%是通过微胞饮内陷发生的。这些结果首次通过一种比较性、定量性的超微结构方法证明,胰岛素和Au-α2MGMA在大鼠脂肪细胞上通过不同的机制进行内吞作用。胰岛素和Au-α2MGMA内吞作用的差异可能与这两种分子不同的生物学作用有关。