Borges Ricardo, Gu Chaoyi, Machado José-David, Ewing Andrew G
Pharmacology Unit, Medical School, Universidad de la Laguna, Tenerife. Spain.
Department of Chemistry and Molecular Biology, University of Gothenburg, Sweden.
Cell Calcium. 2023 Mar;110:102699. doi: 10.1016/j.ceca.2023.102699. Epub 2023 Jan 21.
In this brief review, we discuss the factors that modulate the quantum size and the kinetics of exocytosis. We also discuss the determinants which motivate the type of exocytosis from the so-called kiss-and-run to full fusion and along the intermediate mode of partial release. Kiss-and-run release comprises the transient opening of a nanometer (approx. 2 nm diameter) fusion pore between vesicle and plasma membrane allowing a small amount of release. Partial release comprises a larger more extended opening of the pore to allow a larger fraction of released vesicle content and is what is observed as normal full release in most electrochemical measurements. Partial release appears to be dominant in dense core vesicles and perhaps synaptic vesicles. The concept of partial release leads to the fraction released as a plastic component of exocytosis. Partial vesicular distension and the kinetics of exocytosis can be modulated by second messengers, physiological modulators, and drugs. This concept adds a novel point of regulation for the exocytotic process.
在这篇简短的综述中,我们讨论了调节量子大小和胞吐动力学的因素。我们还讨论了促使胞吐类型从所谓的“亲吻-逃离”到完全融合以及沿着部分释放的中间模式转变的决定因素。“亲吻-逃离”释放包括囊泡与质膜之间纳米级(直径约2纳米)融合孔的短暂开放,允许少量释放。部分释放包括孔的更大、更广泛的开放,以允许更大比例的囊泡内容物释放,这在大多数电化学测量中被视为正常的完全释放。部分释放在致密核心囊泡甚至突触囊泡中似乎占主导地位。部分释放的概念导致释放分数成为胞吐作用的一个可塑性组成部分。部分囊泡扩张和胞吐动力学可受到第二信使、生理调节剂和药物的调节。这一概念为胞吐过程增添了一个新的调节点。