Ilangumaran S, Hoessli D C
Department of Pathology, Centre Médical Universitaire, 1 rue Michel Servet, 1211 Geneva 4, Switzerland.
Biochem J. 1998 Oct 15;335 ( Pt 2)(Pt 2):433-40. doi: 10.1042/bj3350433.
Sphingolipid microdomains are thought to result from the organization of plasma membrane sphingolipids and cholesterol into a liquid ordered phase, wherein the glycosylphosphatidylinositol (GPI)-anchored proteins are enriched. These domains, resistant to extraction by cold Triton X-100, can be isolated as buoyant membrane complexes (detergent-resistant membranes) in isopycnic density gradients. Here the effects of methyl-beta-cyclodextrin (MBCD), a specific cholesterol-binding agent that neither binds nor inserts into the plasma membrane, were investigated on the sphingolipid microdomains of lymphocytes. MBCD released substantial quantities of GPI-anchored Thy-1 and glycosphingolipid GM1, and also other surface proteins including CD45, and intracellular Lck and Fyn kinases. From endothelial cells, MBCD released GPI-anchored CD59, and CD44, but only a negligible amount of caveolin. Most MBCD-released Thy-1 and CD59 were not sedimentable and thus differed from Thy-1 released by membrane-active cholesterol-binding agents such as saponin and streptolysin O, or Triton X-100. Unlike that released by Triton X-100, only part of the Thy-1 molecules released by MBCD was buoyant in density gradients and co-isolated with GM1. Finally, treatment of Triton X-100-isolated detergent-resistant membranes with MBCD extracted most of the cholesterol without affecting the buoyant properties of Thy-1 or GM1. We suggest that (1) MBCD preferentially extracts cholesterol from outside, rather than within the sphingolipid microdomains and (2) this partly solubilizes GPI-anchored and transmembrane proteins from the glycerophospholipid-rich membrane and releases sphingolipid microdomains in both vesicular and non-vesicular form.
鞘脂微区被认为是由质膜鞘脂和胆固醇组织形成液态有序相的结果,其中糖基磷脂酰肌醇(GPI)锚定蛋白富集。这些区域对冷的Triton X-100提取具有抗性,可在等密度梯度中作为漂浮膜复合物(抗去污剂膜)分离出来。在此,研究了甲基-β-环糊精(MBCD),一种既不结合也不插入质膜的特异性胆固醇结合剂,对淋巴细胞鞘脂微区的影响。MBCD释放了大量GPI锚定的Thy-1和糖鞘脂GM1,以及其他表面蛋白,包括CD45,还有细胞内的Lck和Fyn激酶。从内皮细胞中,MBCD释放了GPI锚定的CD59和CD44,但仅释放了可忽略量的小窝蛋白。大多数MBCD释放的Thy-1和CD59不可沉降,因此不同于由膜活性胆固醇结合剂如皂素和链球菌溶血素O或Triton X-100释放的Thy-1。与Triton X-100释放的不同,MBCD释放的Thy-1分子只有一部分在密度梯度中漂浮并与GM1共分离。最后,用MBCD处理Triton X-100分离的抗去污剂膜提取了大部分胆固醇,而不影响Thy-1或GM1的漂浮特性。我们认为:(1)MBCD优先从鞘脂微区外部而非内部提取胆固醇;(2)这部分地使富含甘油磷脂的膜上的GPI锚定蛋白和跨膜蛋白溶解,并以囊泡和非囊泡形式释放鞘脂微区。