Bellini F, Phillips M C, Pickell C, Rothblat G H
Biochim Biophys Acta. 1984 Nov 7;777(2):209-15. doi: 10.1016/0005-2736(84)90422-x.
In order to investigate the role of the plasma membrane in determining the kinetics of removal of cholesterol from cells, the efflux of [3H]cholesterol from intact cells and plasma membrane vesicles has been compared. The release of cholesterol from cultures of Fu5AH rat hepatoma and WIRL-3C rat liver cells to complexes of egg phosphatidylcholine (1 mg/ml) and human high-density apolipoprotein is first order with respect to concentration of cholesterol in the cells, with half-times (t 1/2) for at least one-third of the cell cholesterol of 3.2 +/- 0.6 and 14.3 +/- 1.5 h, respectively. Plasma membrane vesicles (0.5-5.0 micron diameter) were produced from both cell lines by incubating the cells with 50 mM formaldehyde and 2 mM dithiothreitol for 90 min. The efflux of cholesterol from the isolated vesicles follows the same kinetics as the intact, parent cells: the t 1/2 values for plasma membrane vesicles of Fu5AH and WIRL cells are 3.9 +/- 0.5 and 11.2 +/- 0.7 h, respectively. These t 1/2 values reflect the rate-limiting step in the cholesterol efflux process, which is the desorption of cholesterol molecules from the plasma membrane into the extracellular aqueous phase. The fact that intact cells and isolated plasma membranes release cholesterol at the same rates indicates that variations in the plasma membrane structure account for differences in the kinetics of cholesterol release from different cell types. In order to investigate the role of plasma membrane lipids, the kinetics of cholesterol desorption from small unilamellar vesicles prepared from the total lipid isolated from plasma membrane vesicles of Fu5AH and WIRL cells were measured. Half-times of cholesterol release from plasma membrane lipid vesicles of Fu5AH and WIRL cells were the same, with values of 3.1 +/- 0.1 and 2.9 +/- 0.2 h, respectively. Since bilayers formed from isolated plasma membrane lipids do not reproduce the kinetics of cholesterol efflux observed with the intact plasma membranes, it is likely that the local domain structure, as influenced by membrane proteins, is responsible for the differences in t 1/2 values for cholesterol efflux from these cell lines.
为了研究质膜在决定细胞内胆固醇清除动力学方面的作用,已对完整细胞和质膜囊泡中[3H]胆固醇的流出情况进行了比较。Fu5AH大鼠肝癌细胞和WIRL - 3C大鼠肝细胞培养物中的胆固醇释放到卵磷脂酰胆碱(1 mg/ml)和人高密度载脂蛋白的复合物中,相对于细胞内胆固醇浓度而言是一级反应,对于至少三分之一的细胞胆固醇,其半衰期(t1/2)分别为3.2±0.6小时和14.3±1.5小时。通过将细胞与50 mM甲醛和2 mM二硫苏糖醇孵育90分钟,从这两种细胞系中制备出质膜囊泡(直径0.5 - 5.0微米)。从分离的囊泡中流出的胆固醇遵循与完整的亲代细胞相同的动力学:Fu5AH和WIRL细胞的质膜囊泡的t1/2值分别为3.9±0.5小时和11.2±0.7小时。这些t1/2值反映了胆固醇流出过程中的限速步骤,即胆固醇分子从质膜解吸到细胞外水相中。完整细胞和分离的质膜以相同速率释放胆固醇这一事实表明,质膜结构的差异导致了不同细胞类型胆固醇释放动力学的差异。为了研究质膜脂质的作用,测量了从Fu5AH和WIRL细胞的质膜囊泡中分离的总脂质制备的小单层囊泡中胆固醇解吸的动力学。Fu5AH和WIRL细胞质膜脂质囊泡中胆固醇释放的半衰期相同,分别为3.1±0.1小时和2.9±0.2小时。由于由分离的质膜脂质形成的双层膜不能重现完整质膜观察到的胆固醇流出动力学,很可能是受膜蛋白影响的局部结构域导致了这些细胞系胆固醇流出t1/2值的差异。