Aridor M, Rajmilevich G, Beaven M A, Sagi-Eisenberg R
Weizmann Institute of Science, Department of Chemical Immunology, Rehovot, Israel.
Science. 1993 Dec 3;262(5139):1569-72. doi: 10.1126/science.7504324.
Secretagogues of rat peritoneal mast cells, such as mastoparan and compound 48/80, induce mast cell exocytosis by activating directly the guanosine triphosphate-binding proteins that are required for exocytosis. The introduction of a synthetic peptide that corresponds to the carboxyl-terminal end sequence of G alpha i3 into the cells specifically blocked this secretion. Similar results were obtained when antibodies to this peptide were introduced. The G alpha i3 was located in both the Golgi and the plasma membrane, but only the latter source of G alpha i3 appeared to be essential for secretion. These results indicate that G alpha i3 functions to control regulated exocytosis in mast cells.
大鼠腹膜肥大细胞的促分泌素,如mastoparan和化合物48/80,通过直接激活胞吐作用所需的鸟苷三磷酸结合蛋白来诱导肥大细胞胞吐。将一种与Gαi3羧基末端序列相对应的合成肽导入细胞中,可特异性阻断这种分泌。当导入针对该肽的抗体时,也获得了类似的结果。Gαi3存在于高尔基体和质膜中,但似乎只有质膜来源的Gαi3对分泌至关重要。这些结果表明,Gαi3在肥大细胞中发挥控制调节性胞吐的作用。