Fong B S, Rodrigues P O, Angel A
Biochem Cell Biol. 1986 Dec;64(12):1378-82. doi: 10.1139/o86-181.
The specific binding of 125I-labelled low density lipoprotein ([125I]LDL to human adipocyte plasma membranes was higher at 37 than at 0 degree C. Prior treatment of membranes with pronase had no effect on LDL binding measured at 0 degree C but consistently stimulated binding at 37 degrees C. Plasmin was similar to pronase in enhancing LDL-specific binding, but thrombin was not as effective. 125I-labelled high density lipoprotein ([125I]HDL2) specific binding to human adipocyte plasma membranes was similarly sensitive to temperature and pronase treatment. Addition of the protease inhibitor aprotinin in the adipocyte membrane binding assay significantly reduced [125I]LDL binding at 37 degrees C (p less than 0.05), suggesting the involvement of a protease activity intrinsic to the lipoproteins and (or) membranes. These data demonstrate that both LDL and HDL binding in human adipocyte plasma membranes can be "up-regulated" by specific proteolytic perturbations in a temperature-dependent manner.
125I标记的低密度脂蛋白([125I]LDL)与人脂肪细胞质膜的特异性结合在37℃时高于0℃。用链霉蛋白酶预先处理膜对在0℃时测定的LDL结合没有影响,但在37℃时持续刺激结合。纤溶酶在增强LDL特异性结合方面与链霉蛋白酶相似,但凝血酶效果较差。125I标记的高密度脂蛋白([125I]HDL2)与人脂肪细胞质膜的特异性结合对温度和链霉蛋白酶处理同样敏感。在脂肪细胞膜结合试验中加入蛋白酶抑制剂抑肽酶显著降低了37℃时的[125I]LDL结合(p<0.05),提示脂蛋白和(或)膜固有的蛋白酶活性参与其中。这些数据表明,人脂肪细胞质膜中LDL和HDL的结合均可通过特定的蛋白水解扰动以温度依赖的方式“上调”。