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分泌控制的新见解。

New insights into the control of secretion.

作者信息

Thorn Peter

机构信息

School of Biomedical Sciences; University of Queensland; St. Lucia, Queensland Australia.

出版信息

Commun Integr Biol. 2009 Jul;2(4):315-7. doi: 10.4161/cib.2.4.8262.

Abstract

Vesicular secretion is a fundamental process in the body with vesicle fusion releasing vesicle contents to the outside. This process called exocytosis is usually thought of as leading to an all-or-none release of content; regulation of secretory output dependent on regulating the numbers of fused vesicles. However, it is well established that the fusion pore that forms when the vesicle membrane fuses with the cell membrane is dynamic. More recent evidence indicates the dynamic opening and closing, and the size of the fusion pore, are limiting factors to the release of vesicle content. What remains unclear is whether these fusion pore behaviors are under cellular control and therefore relevant to cell physiology.Accumulating evidence over the last two years points to myosin 2 as one regulator of fusion pore behavior. This is interesting since myosin 2 activity is in turn controlled by kinases and phosphatases, well known to be under cellular control. We conclude that fusion pore behavior is likely a genuine control point for vesicle content release. This leads to a model for secretion with secretory output controlled not only by the numbers of vesicles fused but also by the regulation of the behavior of individual vesicles.

摘要

囊泡分泌是机体的一个基本过程,囊泡融合将囊泡内容物释放到细胞外。这个称为胞吐作用的过程通常被认为会导致内容物的全或无释放;分泌输出的调节取决于对融合囊泡数量的调节。然而,已经明确的是,当囊泡膜与细胞膜融合时形成的融合孔是动态的。最近的证据表明,融合孔的动态开闭以及大小是囊泡内容物释放的限制因素。尚不清楚的是,这些融合孔行为是否受细胞控制,因此与细胞生理学相关。过去两年积累的证据表明,肌球蛋白2是融合孔行为的一种调节因子。这很有意思,因为肌球蛋白2的活性反过来又受激酶和磷酸酶的控制,而激酶和磷酸酶众所周知受细胞控制。我们得出结论,融合孔行为可能是囊泡内容物释放的一个真正控制点。这就产生了一个分泌模型,其中分泌输出不仅受融合囊泡数量的控制,还受单个囊泡行为调节的控制。

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