Gratzl M, Dahl G, Russell J T, Thorn N A
Biochim Biophys Acta. 1977 Oct 3;470(1):45-57. doi: 10.1016/0005-2736(77)90060-8.
Freeze cleaving electron microscopy has shown that fusion of isolated secretory vesicles from bovine neurohypophyses was induced by Ca2+ in micromolar concentrations. Mg2+ and Sr2+ were ineffective. Mg2+ inhibited Ca2+-induced fusion. In suspensions containing secretory vesicles as well as sheets of cell membrane, release of vasopressin parallel to intervesicular fusion and fusion of secretory vesicles with sheets of cell membrane was observed after exposure to Ca2+. Mg2+ and Sr2+ were ineffective in replacing Ca2+ as trigger for fusion or vasopressin release. Intervesicular fusion and exocytotic profiles were observed when isolated neurohypophyses or neurosecretosomes were exposed to cold.
冷冻蚀刻电子显微镜显示,微摩尔浓度的Ca2+可诱导来自牛神经垂体的分离分泌囊泡融合。Mg2+和Sr2+无效。Mg2+抑制Ca2+诱导的融合。在含有分泌囊泡和细胞膜片的悬浮液中,暴露于Ca2+后,观察到与囊泡间融合平行的加压素释放以及分泌囊泡与细胞膜片的融合。Mg2+和Sr2+不能有效替代Ca2+作为融合或加压素释放的触发因素。当分离的神经垂体或神经分泌小体暴露于低温时,可观察到囊泡间融合和胞吐现象。