Jolicoeur M, Kan F W, Paiement J
Département d'Anatomie, Université de Montreal, Québec, Canada.
J Histochem Cytochem. 1991 Mar;39(3):363-72. doi: 10.1177/39.3.1993830.
Using detergent-free conditions of incubation for the analysis of liponucleotide synthesis, we compared GTP-dependent formation of CDP-diacylglycerol (CDP-DG) and membrane fusion in RNA-depleted rough microsomes from rat liver. After incubation of stripped rough microsomes (SRM) in the presence of GTP and [5-3H]-CTP, radioactivity was recovered in lipid extracts and identified by thin-layer chromatography as a single spot which co-migrated with CDP-DG. The nucleotide requirement for CDP-DG synthesis and that for membrane fusion were observed to be identical. We next carried out an electron microscopic autoradiographic analysis on incubated membranes to determine the site of incorporation of [5-3H]-CTP. Silver grains were observed directly over the unilamellar membranes of natural vesicles. In confirmation of the biochemical data, quantitation of silver grain density indicated more grains over membranes incubated in the presence of GTP than over those incubated in the absence of this nucleotide. For membranes incubated in the presence of GTP, the grain density was similar over fused and unfused membranes in the same preparation. When SRM were incubated with the enzyme co-factors required for synthesis of phosphatidylinositol, a GTP-independent membrane fusion was observed by both transmission and freeze-fracture electron microscopy. Together with the biochemical and autoradiographic data, this suggests that phospholipid metabolism may be activated by GTP and lead to the fusion of RER membrane.
在无去污剂的孵育条件下分析脂核苷酸合成,我们比较了大鼠肝脏RNA缺失的糙面微粒体中CDP - 二酰甘油(CDP - DG)的GTP依赖性形成和膜融合。在GTP和[5 - ³H] - CTP存在下孵育脱脂糙面微粒体(SRM)后,放射性在脂质提取物中回收,并通过薄层色谱鉴定为与CDP - DG共迁移的单个斑点。观察到CDP - DG合成和膜融合的核苷酸需求是相同的。接下来,我们对孵育后的膜进行了电子显微镜放射自显影分析,以确定[5 - ³H] - CTP的掺入位点。在天然囊泡的单层膜上直接观察到银颗粒。为了证实生化数据,银颗粒密度的定量分析表明,在GTP存在下孵育的膜上的颗粒比在无此核苷酸孵育的膜上更多。对于在GTP存在下孵育的膜,同一制剂中融合膜和未融合膜上的颗粒密度相似。当SRM与磷脂酰肌醇合成所需的酶辅因子一起孵育时,通过透射电子显微镜和冷冻断裂电子显微镜均观察到了不依赖GTP的膜融合。结合生化和放射自显影数据,这表明磷脂代谢可能被GTP激活并导致内质网(RER)膜融合。