Slotte J P, Hedström G, Rannström S, Ekman S
Department of Biochemistry and Pharmacy, Abo Akademi, Turku, Finland.
Biochim Biophys Acta. 1989 Oct 2;985(1):90-6. doi: 10.1016/0005-2736(89)90108-9.
This study addresses questions related to (i) the distribution of cholesterol between the cell surface and intracellular membranes in cultured fibroblasts and (ii) the effects of plasma membrane sphingomyelin on this distribution. Cholesterol oxidase (Streptomyces sp.) converts cell cholesterol to cholestenone and was used in this study to probe the cellular distribution of cholesterol. The availability of cell cholesterol for oxidation by cholesterol oxidase was markedly influenced by the presence of sphingomyelin. In native, glutaraldehyde-fixed fibroblasts only about 20% of the cell cholesterol was oxidized under our experimental conditions. However, degradation of cell sphingomyelin with sphingomyelinase (Staphylococcus aureus) markedly enhanced the oxidation of cell surface cholesterol in glutaraldehyde-fixed fibroblasts. About 90% of the total unesterified cholesterol could be oxidized to cholestenone in confluent, sphingomyelin-depleted fibroblasts. These results suggest that about 90% of the unesterified cholesterol was at the cell surface in these cells. It was also observed that degradation of cell sphingomyelin exerted a dramatic effect on the distribution of cell cholesterol between the cell surface and intracellular membranes. Within 90 min after hydrolysis of cell sphingomyelin, about 30% of the total cell-associated unesterified cholesterol was transported from a cholesterol oxidase-susceptible pool to an oxidase-resistant pool. Together with the redistribution of cell cholesterol after sphingomyelin degradation, a marked enhancement of the endogenous cholesterol esterification reaction was observed. We conclude that the degradation of plasma membrane sphingomyelin resulted in a new apparent steady-state distribution of cellular cholesterol, with less cholesterol in the plasma membrane and more in intracellular membranes. It therefore appears that sphingomyelin is a major determinant of the distribution of cholesterol in intact cells.
(i)培养的成纤维细胞中胆固醇在细胞表面和细胞内膜之间的分布;(ii)质膜鞘磷脂对这种分布的影响。胆固醇氧化酶(链霉菌属)将细胞胆固醇转化为胆甾烯酮,本研究用其来探究胆固醇的细胞内分布。鞘磷脂的存在显著影响了细胞胆固醇被胆固醇氧化酶氧化的可用性。在天然的、经戊二醛固定的成纤维细胞中,在我们的实验条件下,只有约20%的细胞胆固醇被氧化。然而,用鞘磷脂酶(金黄色葡萄球菌)降解细胞鞘磷脂,可显著增强戊二醛固定的成纤维细胞表面胆固醇的氧化。在汇合的、鞘磷脂耗尽的成纤维细胞中,约90%的总游离胆固醇可被氧化为胆甾烯酮。这些结果表明,在这些细胞中约90%的游离胆固醇位于细胞表面。还观察到,细胞鞘磷脂的降解对细胞胆固醇在细胞表面和细胞内膜之间的分布产生了显著影响。在细胞鞘磷脂水解后90分钟内,约30%的与细胞相关的总游离胆固醇从胆固醇氧化酶敏感池转运至氧化酶抗性池。随着鞘磷脂降解后细胞胆固醇的重新分布,观察到内源性胆固醇酯化反应显著增强。我们得出结论,质膜鞘磷脂的降解导致了细胞胆固醇新的表观稳态分布,质膜中胆固醇减少,细胞内膜中胆固醇增多。因此,鞘磷脂似乎是完整细胞中胆固醇分布的主要决定因素。