Hahn S E, Parkes J G, Goldberg D M
Department of Clinical Biochemistry, University of Toronto, Banting Institute, Ont., Canada.
Biochem Cell Biol. 1992 Dec;70(12):1339-46. doi: 10.1139/o92-182.
Hep G2 cells were used to study the relationship between apolipoprotein synthesis and secretion, as revealed by their interaction with agents modulating these processes. Cycloheximide inhibited the secretion of both apolipoproteins (apo) AI and B, but the reduction in apo AI secretion was evident at earlier times. Monensin also inhibited secretion of apo AI and apo B, but only apo AI accumulated intracellularly. Pulse-chase studies showed that, at concentrations of monensin that had no effect on total protein synthesis, apo B synthesis was specifically inhibited. Triacylglycerol synthesis was inhibited to the same extent as apo B synthesis, but this preceded the latter inhibition and unlike apo B there was an accumulation of intracellular triglyceride. These results suggest that distinctive mechanisms modulate the synthesis and secretion of apo AI and apo B, and that apo B synthesis can be specifically inhibited by mechanisms that initially block triglyceride production.
利用Hep G2细胞研究载脂蛋白合成与分泌之间的关系,这一关系通过它们与调节这些过程的试剂的相互作用得以揭示。放线菌酮抑制载脂蛋白(apo)AI和B的分泌,但apo AI分泌的减少在较早时间就很明显。莫能菌素也抑制apo AI和apo B的分泌,但只有apo AI在细胞内积累。脉冲追踪研究表明,在对总蛋白合成无影响的莫能菌素浓度下,apo B合成受到特异性抑制。三酰甘油合成受到的抑制程度与apo B合成相同,但这在后者抑制之前发生,并且与apo B不同的是,细胞内甘油三酯有积累。这些结果表明,不同的机制调节apo AI和apo B的合成与分泌,并且apo B合成可被最初阻断甘油三酯产生的机制特异性抑制。