Llobet Artur, Wu Minnie, Lagnado Leon
Medical Research Council Laboratory of Molecular Biology, Cambridge, England, UK.
J Cell Biol. 2008 Sep 8;182(5):1017-28. doi: 10.1083/jcb.200807034.
Secretion of hormones and peptides by neuroendocrine cells occurs through fast and slow modes of vesicle fusion but the mechanics of these processes are not understood. We used interference reflection microscopy to monitor deformations of the membrane surface and found that both modes of fusion involve the tightly coupled dilation and constriction of the vesicle. The rate of opening is calcium dependent and occurs rapidly at concentrations <5 muM [corrected] The fast mode of fusion is blocked selectively by a truncation mutant of amphiphysin. Vesicles do not collapse when fusion is triggered by strontium, rather they remain locked open and membrane scission is blocked. In contrast, constriction of the vesicle opening continues when endocytosis is blocked by inhibiting the function of dynamin. Thus, fast and slow modes of fusion involve similar membrane deformations and vesicle closure can be uncoupled from membrane scission. Regulation of these processes by calcium and amphiphysin may provide a mechanism for controlling the release of vesicle contents.
神经内分泌细胞分泌激素和肽是通过囊泡融合的快速和慢速模式进行的,但这些过程的机制尚不清楚。我们使用干涉反射显微镜来监测膜表面的变形,发现两种融合模式都涉及囊泡紧密耦合的扩张和收缩。开口速率依赖于钙,在浓度<5μM[校正后]时迅速发生。快速融合模式被 amphiphysin 的截短突变体选择性阻断。当由锶触发融合时,囊泡不会塌陷,而是保持锁定开放状态,膜分裂被阻断。相反,当通过抑制发动蛋白的功能来阻断内吞作用时,囊泡开口的收缩仍会继续。因此,快速和慢速融合模式涉及相似的膜变形,并且囊泡闭合可以与膜分裂解偶联。钙和 amphiphysin 对这些过程的调节可能为控制囊泡内容物的释放提供一种机制。