Esfahani M, Scerbo L, Lund-Katz S, DePace D M, Maniglia R, Alexander J K, Phillips M C
Biochim Biophys Acta. 1986 Dec 19;889(3):287-300. doi: 10.1016/0167-4889(86)90191-6.
The human monocyte/macrophage-like cell line U937 is a cholesterol auxotroph. Incubation of these cells in the growth medium in which delipidated fetal calf serum has been substituted for fetal calf serum depletes cellular cholesterol and inhibits growth. The cholesterol requirement of these cells for growth can be satisfied by human low-density lipoprotein (LDL), and very-low-density lipoprotein (VLDL), but not by high-density lipoprotein (HDL). U937 cells can bind and degrade LDL via a high-affinity site and this recognition is altered by acetylation of LDL. This indicates that these cells express relatively high LDL receptor activity and low levels of the acetyl-LDL receptor. The cells were used to study the role of cholesterol in lectin-mediated and fluid-phase endocytosis. Growth of the cells in the medium containing delipidated fetal calf serum results in impairment of both concanavalin A-mediated endocytosis of horseradish peroxidase and concanavalin A-independent endocytosis of Lucifer Yellow. Supplementation of the medium with cholesterol prevents cellular cholesterol depletion, supports growth and stimulates Lucifer Yellow endocytosis but fails to restore horseradish peroxidase endocytosis. However, if the cells are incubated in the presence of no less than 40 micrograms LDL protein/ml to maintain normal cell cholesterol levels, concanavalin A-mediated endocytosis of horseradish peroxidase is activated. The effect of LDL is specific since neither VLDL nor HDL3 at the same protein concentration activates horseradish peroxidase uptake by the cells. Furthermore, the activation of endocytosis by LDL is not inhibited by the inclusion of heparin or acetylation of the LDL indicating that binding of LDL to the LDL receptor is not required for these effects. The mediation of activation of horseradish peroxidase endocytosis by the lectin is presumed to involve binding of LDL to concanavalin A associated with the cell surface which in turn stimulates horseradish peroxidase binding and uptake by adsorptive endocytosis. The rate of fluid endocytosis and endosome formation seems to depend on cellular cholesterol content presumably because cholesterol is involved in maintaining the appropriate plasma membrane structure and fluidity.
人单核细胞/巨噬细胞样细胞系U937是一种胆固醇营养缺陷型细胞。将这些细胞在已用脱脂胎牛血清替代胎牛血清的生长培养基中培养,会耗尽细胞内的胆固醇并抑制生长。这些细胞生长所需的胆固醇可由人低密度脂蛋白(LDL)和极低密度脂蛋白(VLDL)满足,但不能由高密度脂蛋白(HDL)满足。U937细胞可通过高亲和力位点结合并降解LDL,且这种识别会因LDL的乙酰化而改变。这表明这些细胞表达相对较高的LDL受体活性和较低水平的乙酰化LDL受体。这些细胞被用于研究胆固醇在凝集素介导的和液相内吞作用中的作用。在含有脱脂胎牛血清的培养基中培养细胞会导致伴刀豆球蛋白A介导的辣根过氧化物酶内吞作用和伴刀豆球蛋白A非依赖性的荧光素黄内吞作用受损。向培养基中补充胆固醇可防止细胞内胆固醇耗尽,支持细胞生长并刺激荧光素黄内吞作用,但无法恢复辣根过氧化物酶内吞作用。然而,如果将细胞在不低于40微克LDL蛋白/毫升的条件下孵育以维持正常的细胞胆固醇水平,则伴刀豆球蛋白A介导的辣根过氧化物酶内吞作用会被激活。LDL的作用具有特异性,因为相同蛋白浓度的VLDL和HDL3均不能激活细胞对辣根过氧化物酶的摄取。此外,LDL对内吞作用的激活不受肝素的加入或LDL乙酰化的抑制,这表明这些效应不需要LDL与LDL受体结合。推测凝集素对辣根过氧化物酶内吞作用激活的介导涉及LDL与细胞表面相关的伴刀豆球蛋白A的结合,这反过来又通过吸附性内吞作用刺激辣根过氧化物酶的结合和摄取。液相内吞作用和内体形成的速率似乎取决于细胞内胆固醇含量, 大概是因为胆固醇参与维持适当的质膜结构和流动性。