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Bilayers merge even when exocytosis is transient

机译:即使在胞吐作用短暂时,双层也会合并

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During exocytosis, the lumen of secretory vesicles, connects with the extracellular space. In some vesicles, this connection closes again, causing the vesicle to be recaptured mostly intact. The degree to which the bilayers of such vesicles mix with the plasma membrane is unknown. Work supporting the kiss-and-run model of transient exocytosis implies that synaptic vesicles allow neither lipid nor protein to escape into the plasma membrane, suggesting that the two bilayers never merge. Here, we test whether neuroendocrine granules behave similarly. Using two-color evanescent field microscopy, we imaged the lipid probe FM4-64 and fluorescent proteins in single dense core granules. During exocytosis, granules lost FM4-64 into the plasma membrane in small fractions of a second. Although FM4-64 was lost, granules retained the membrane protein, GFP-phogrin. By using GFP-phogrin as a probe for resealing, it was found that even granules that reseal lose FM4-64. We conclude that the lipid bilayers of the granule and the plasma membrane become continuous even when exocytosis is transient.
机译:在胞吐过程中,分泌囊泡的内腔与细胞外空间相连。在某些囊泡中,该连接再次关闭,从而使囊泡几乎完整地被重新捕获。这种囊泡的双层与质膜混合的程度是未知的。支持瞬时胞吐作用的接吻运行模式的工作表明,突触囊泡既不允许脂质也不能蛋白质逃逸进入质膜,表明这两个双层从未融合。在这里,我们测试神经内分泌颗粒是否表现相似。使用两色渐逝场显微镜,我们在单个致密核心颗粒中成像了脂质探针FM4-64和荧光蛋白。在胞吐过程中,颗粒在短短的几分之一秒内就将FM4-64损失到质膜中。尽管FM4-64丢失了,但是颗粒保留了膜蛋白GFP-凝集素。通过使用GFP-凝集素作为重新密封的探针,发现即使重新密封的颗粒也会损失FM4-64。我们得出结论,即使胞吐作用是短暂的,颗粒和质膜的脂质双层也变得连续。

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