Oda K, Fujiwara T, Ikehara Y
Department of Biochemistry, Fukuoka University School of Medicine, Japan.
Biochem J. 1990 Jan 1;265(1):161-7. doi: 10.1042/bj2650161.
We have studied the effect of brefeldin A (BFA) on the intracellular transport of the envelope proteins of vesicular stomatitis virus (VSV) and sindbis virus in primary cultured rat hepatocytes. BFA (2.5 micrograms/ml) inhibited not only the secretion of plasma proteins into the medium, but also the assembly of both G protein of VSV and E1 and E2 proteins (envelope proteins) of sindbis virus into respective virions. Concomitantly, both the acquisition of endo-beta-N-acetylglucosaminidase H resistance by the G protein and the proteolytic conversion of PE2 to E2 were found to be inhibited in the BFA-treated cells, suggesting that the intracellular transport of the envelope proteins was arrested in the endoplasmic reticulum. Such inhibitory effects of the drug were variable depending upon the culture conditions of the hepatocytes. In the 1-day-cultured cells, even in the presence of the drug, newly synthesized envelope proteins were assembled into the virions after a 3 h chase period, at the same time as secretion of plasma proteins into the medium resumes. In contrast, in 4-day-cultured hepatocytes, BFA continuously blocked the entry of the envelope proteins into the virions and the release of plasma proteins into the medium for at least 5 h. BFA also completely inhibited the exocytotic pathway in HepG2 cells. These results indicate that the duration time of the effect of BFA is different from one cell to another and may change depending upon the culture conditions of the cells.
我们研究了布雷菲德菌素A(BFA)对原代培养大鼠肝细胞中水泡性口炎病毒(VSV)和辛德毕斯病毒包膜蛋白细胞内运输的影响。BFA(2.5微克/毫升)不仅抑制血浆蛋白分泌到培养基中,还抑制VSV的G蛋白以及辛德毕斯病毒的E1和E2蛋白(包膜蛋白)组装到各自的病毒颗粒中。同时,在经BFA处理的细胞中,发现G蛋白获得内切β-N-乙酰葡糖胺糖苷酶H抗性以及PE2向E2的蛋白水解转化均受到抑制,这表明包膜蛋白的细胞内运输在内质网中停滞。药物的这种抑制作用因肝细胞的培养条件而异。在培养1天的细胞中,即使存在该药物,新合成的包膜蛋白在3小时的追踪期后仍会组装到病毒颗粒中,与此同时血浆蛋白恢复分泌到培养基中。相比之下,在培养4天的肝细胞中,BFA至少持续5小时阻断包膜蛋白进入病毒颗粒以及血浆蛋白释放到培养基中。BFA还完全抑制了HepG2细胞中的胞吐途径。这些结果表明,BFA作用的持续时间因细胞而异,并且可能根据细胞的培养条件而改变。