原代大鼠脂肪细胞小窝及周围质膜中的脂质和糖鞘脂。
Lipids and glycosphingolipids in caveolae and surrounding plasma membrane of primary rat adipocytes.
作者信息
Ortegren Unn, Karlsson Margareta, Blazic Natascha, Blomqvist Maria, Nystrom Fredrik H, Gustavsson Johanna, Fredman Pam, Strålfors Peter
机构信息
Department of Cell Biology and Diabetes Research Centre, Linköping University, Sweden.
出版信息
Eur J Biochem. 2004 May;271(10):2028-36. doi: 10.1111/j.1432-1033.2004.04117.x.
We have made a comprehensive and quantitative analysis of the lipid composition of caveolae from primary rat fat cells and compared the composition of plasma membrane inside and outside caveolae. We isolated caveolae from purified plasma membranes using ultrasonication in carbonate buffer to disrupt the membrane, or extraction with nonionic detergent, followed by density gradient ultracentrifugation. The carbonate-isolated caveolae fraction was further immunopurified using caveolin antibodies. Carbonate-isolated caveolae were enriched in cholesterol and sphingomyelin, and the concentration was three- and twofold higher, respectively, in caveolae compared to the surrounding plasma membrane. The concentration of glycerophospholipids was similar suggesting that glycerophospholipids constitute a constant core throughout the plasma membrane. The composition of detergent-insoluble fractions of the plasma membrane was very variable between preparations, but strongly enriched in sphingomyelin and depleted of glycerophospholipids compared to carbonate-isolated caveolae; indicating that detergent extraction is not a suitable technique for caveolae preparation. An average adipocyte caveola contained about 22 x 10(3) molecules of cholesterol, 7.5 x 10(3) of sphingomyelin and 23 x 10(3) of glycerophospholipid. The glycosphingolipid GD3 was highly enriched in caveolae, whereas GM3, GM1 and GD1a were present inside as well as outside the caveolae membrane. GD1b, GT1b, GM2, GQ1b, sulfatide and lactosylceramide sulfate were not detected in caveolae.
我们对原代大鼠脂肪细胞小窝的脂质组成进行了全面定量分析,并比较了小窝内外质膜的组成。我们使用碳酸盐缓冲液中的超声处理破坏膜,或用非离子去污剂提取,随后进行密度梯度超速离心,从纯化的质膜中分离出小窝。用小窝蛋白抗体对碳酸盐分离的小窝部分进行进一步免疫纯化。碳酸盐分离的小窝富含胆固醇和鞘磷脂,与周围质膜相比,小窝中的浓度分别高出三倍和两倍。甘油磷脂的浓度相似,表明甘油磷脂在整个质膜中构成一个恒定的核心。质膜去污剂不溶性部分的组成在不同制剂之间变化很大,但与碳酸盐分离的小窝相比,鞘磷脂含量显著增加,甘油磷脂含量减少;这表明去污剂提取不是制备小窝的合适技术。一个平均脂肪细胞小窝含有约22×10³个胆固醇分子、7.5×10³个鞘磷脂分子和23×10³个甘油磷脂分子。糖鞘脂GD3在小窝中高度富集,而GM3、GM1和GD1a在小窝膜内外均有存在。在小窝中未检测到GD1b、GT1b、GM2、GQ1b、硫苷脂和乳糖基硫酸神经酰胺。