Scherer P E, Lisanti M P, Baldini G, Sargiacomo M, Mastick C C, Lodish H F
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142-1479.
J Cell Biol. 1994 Dec;127(5):1233-43. doi: 10.1083/jcb.127.5.1233.
Caveolae, also termed plasmalemmal vesicles, are small, flask-shaped, non-clathrin-coated invaginations of the plasma membrane. Caveolin is a principal component of the filaments that make up the striated coat of caveolae. Using caveolin as a marker protein for the organelle, we found that adipose tissue is the single most abundant source of caveolae identified thus far. Caveolin mRNA and protein are strongly induced during differentiation of 3T3-L1 fibroblasts to adipocytes; during adipogenesis there is also a dramatic increase in the complexity of the protein composition of caveolin-rich membrane domains. About 10-15% of the insulin-responsive glucose transporter GLUT4 is found in this caveolin-rich fraction, and immuno-isolated vesicles containing GLUT4 also contain caveolin. However, in non-stimulated adipocytes the majority of caveolin fractionates with the plasma membrane, while most GLUT4 associates with low-density microsomes. Upon addition of insulin to 3T3-L1 adipocytes, there is a significant increase in the amount of GLUT4 associated with caveolin-rich membrane domains, an increase in the amount of caveolin associated with the plasma membrane, and a decrease in the amount of caveolin associated with low-density microsomes. Caveolin does not undergo a change in phosphorylation upon stimulation of 3T3-L1 adipocytes with insulin. However, after treatment with insulin it is associated with a 32-kD phosphorylated protein. Caveolae thus may play an important role in the vesicular transport of GLUT4 to or from the plasma membrane. 3T3-L1 adipocytes offer an attractive system to study the function of caveolae in several cellular trafficking and signaling events.
小窝,也称为质膜小泡,是质膜上小的、烧瓶状、无网格蛋白包被的内陷结构。小窝蛋白是构成小窝条纹状包被的细丝的主要成分。以小窝蛋白作为该细胞器的标记蛋白,我们发现脂肪组织是迄今为止已确定的小窝最丰富的单一来源。在3T3-L1成纤维细胞向脂肪细胞分化过程中,小窝蛋白mRNA和蛋白被强烈诱导;在脂肪生成过程中,富含小窝蛋白的膜结构域的蛋白质组成复杂性也显著增加。约10%-15%的胰岛素反应性葡萄糖转运体GLUT4存在于这个富含小窝蛋白的组分中,免疫分离得到的含有GLUT4的小泡也含有小窝蛋白。然而,在未受刺激的脂肪细胞中,大部分小窝蛋白与质膜分离,而大多数GLUT4与低密度微粒体结合。向3T3-L1脂肪细胞中添加胰岛素后,与富含小窝蛋白的膜结构域结合的GLUT4量显著增加,与质膜结合的小窝蛋白量增加,与低密度微粒体结合 的小窝蛋白量减少。用胰岛素刺激后,小窝蛋白的磷酸化状态没有改变。然而,胰岛素处理后,它与一种32-kD的磷酸化蛋白相关。因此,小窝可能在GLUT4往返质膜的囊泡运输中起重要作用。3T3-L1脂肪细胞为研究小窝在几种细胞运输和信号转导事件中的功能提供了一个有吸引力 的系统。