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ADP-核糖基化因子对大鼠下颌下腺腺泡细胞中磷脂酶D的激活作用。

Activation of phospholipase D by ADP-ribosylation factor in rat submandibular acinar cells.

作者信息

Li L, Mellow L, Bhullar R P, Fleming N

机构信息

Department of Oral Biology, University of Manitoba, Winnipeg, Canada.

出版信息

Arch Oral Biol. 1998 Mar;43(3):211-9. doi: 10.1016/s0003-9969(98)00007-7.

Abstract

The hydrolysis of membrane phosphatidylcholine by the enzyme phospholipase D is a key initial step in the intracellular release of the signalling molecules phosphatidic acid, diacylglycerol and arachidonic acid. Guanine nucleotide-dependent pathway leading to PLD activation were investigated in enzymatically dispersed rat submandibular acinar cells. Guanosine 5'-O-[gamma-thio]triphosphate (GTP gamma S) caused the time- and concentration-dependent stimulation of PLD in permeabilized cells. This effect was lost in prepermeabilized cells, from which cytosolic components had been allowed to leak, but was restored when endogenous cytosol, or cytosol from platelets, was added back to such cells. PLD was also activated in cytosol-depleted cells by GTP gamma S in combination with purified ARF (ADP-ribosylation factor), a low M(r) guanine nucleotide-binding protein of the ras superfamily. Additional evidence for the involvement of ARF in PLD activation was the inhibition of carbachol- or GTP gamma S-induced stimulation of the enzyme by brefeldin A, a blocker of ARF activation; and the observed translocation of ARF from cytosol to membrane on GTP gamma S treatment in permeabilized cells. The heterotrimeric G-protein stimulator, AlFn, also activated PLD, and this response, too, was inhibited by brefeldin A, suggesting the downstream involvement of ARF in coupling AlFn action to phospholipase D elevation. PLD activation caused by both GTP gamma S and AlFn was only partially reduced after treatment of cells with U73122, a demonstrated inhibitor of phospholipase C in the Gq-coupled phosphoinositide signal-transduction pathway. It is therefore proposed that in rat submandibular mucous acinar cells, a guanine nucleotide-regulated PLD activation pathway exists that involves the sequential actions of a G heterotrimeric protein and ARF. It is further suggested that this pathway is independent of the Gq/PLC/phosphatidylinositol signal transduction system.

摘要

磷脂酶D对膜磷脂酰胆碱的水解作用是信号分子磷脂酸、二酰基甘油和花生四烯酸细胞内释放过程中的关键起始步骤。在酶解分散的大鼠下颌下腺腺泡细胞中研究了导致磷脂酶D激活的鸟嘌呤核苷酸依赖性途径。鸟苷5'-O-[γ-硫代]三磷酸(GTPγS)在通透细胞中引起磷脂酶D的时间和浓度依赖性刺激。这种效应在预通透细胞中消失,预通透细胞的胞质成分已泄漏,但当向这些细胞中重新添加内源性胞质溶胶或血小板胞质溶胶时,效应得以恢复。在缺乏胞质溶胶的细胞中,GTPγS与纯化的ARF(ADP-核糖基化因子,一种ras超家族的低分子量鸟嘌呤核苷酸结合蛋白)联合也能激活磷脂酶D。ARF参与磷脂酶D激活的其他证据包括:布雷菲德菌素A(一种ARF激活阻滞剂)对卡巴胆碱或GTPγS诱导的该酶刺激的抑制作用;以及在通透细胞中用GTPγS处理后观察到ARF从胞质溶胶向膜的转位。异源三聚体G蛋白刺激剂AlFn也能激活磷脂酶D,并且这种反应也被布雷菲德菌素A抑制,提示ARF在将AlFn的作用与磷脂酶D升高偶联中起下游作用。在用U73122(一种已证实的Gq偶联磷酸肌醇信号转导途径中磷脂酶C的抑制剂)处理细胞后,GTPγS和AlFn引起的磷脂酶D激活仅部分降低。因此提出,在大鼠下颌下黏液腺泡细胞中,存在一种鸟嘌呤核苷酸调节的磷脂酶D激活途径,该途径涉及异源三聚体G蛋白和ARF的顺序作用。进一步提示该途径独立于Gq/磷脂酶C/磷脂酰肌醇信号转导系统。

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