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本文引用的文献

1
Hyperpolarization-activated cyclic nucleotide-gated channels and cAMP-dependent modulation of exocytosis in cultured rat lactotrophs.极化激活环核苷酸门控通道和 cAMP 依赖性调节培养的大鼠催乳细胞分泌。
J Neurosci. 2014 Nov 19;34(47):15638-47. doi: 10.1523/JNEUROSCI.5290-13.2014.
2
Extracellular Ca²⁺ per se inhibits quantal size of catecholamine release in adrenal slice chromaffin cells.细胞外钙离子本身可抑制肾上腺切片嗜铬细胞中儿茶酚胺释放的量子大小。
Cell Calcium. 2014 Sep;56(3):202-7. doi: 10.1016/j.ceca.2014.07.006. Epub 2014 Jul 22.
3
Complexin synchronizes primed vesicle exocytosis and regulates fusion pore dynamics.衔接蛋白协调预融合囊泡的胞吐作用,并调节融合孔动力学。
J Cell Biol. 2014 Mar 31;204(7):1123-40. doi: 10.1083/jcb.201311085.
4
High-resolution membrane capacitance measurements for the study of exocytosis and endocytosis.高分辨率膜电容测量在胞吐作用和胞吞作用研究中的应用。
Nat Protoc. 2013 Jun;8(6):1169-83. doi: 10.1038/nprot.2013.069. Epub 2013 May 23.
5
cAMP-mediated stabilization of fusion pores in cultured rat pituitary lactotrophs.cAMP 介导的培养的大鼠垂体泌乳素细胞融合孔的稳定化。
J Neurosci. 2013 May 1;33(18):8068-78. doi: 10.1523/JNEUROSCI.5351-12.2013.
6
Fusion pore formation and expansion induced by Ca2+ and synaptotagmin 1.钙离子和突触融合蛋白 1 诱导的融合孔形成和扩张。
Proc Natl Acad Sci U S A. 2013 Jan 22;110(4):1333-8. doi: 10.1073/pnas.1218818110. Epub 2013 Jan 8.
7
Regulated exocytosis per partes.有部分调节的胞吐作用。
Cell Calcium. 2012 Sep-Oct;52(3-4):191-5. doi: 10.1016/j.ceca.2012.06.003. Epub 2012 Jul 9.
8
Cholesterol and regulated exocytosis: a requirement for unitary exocytotic events.胆固醇与调节性胞吐作用:单位胞吐事件的必需条件。
Cell Calcium. 2012 Sep-Oct;52(3-4):250-8. doi: 10.1016/j.ceca.2012.05.009. Epub 2012 Jun 20.
9
Exocytosis in astrocytes: transmitter release and membrane signal regulation.星形胶质细胞中的胞吐作用:递质释放和膜信号调节。
Neurochem Res. 2012 Nov;37(11):2351-63. doi: 10.1007/s11064-012-0773-6. Epub 2012 Apr 21.
10
Fusion pore diameter regulation by cations modulating local membrane anisotropy.阳离子通过调节局部膜各向异性来调控融合孔直径。
ScientificWorldJournal. 2012;2012:983138. doi: 10.1100/2012/983138. Epub 2012 Mar 12.

局部静电相互作用决定融合孔的直径。

Local electrostatic interactions determine the diameter of fusion pores.

作者信息

Guček Alenka, Jorgačevski Jernej, Górska Urszula, Rituper Boštjan, Kreft Marko, Zorec Robert

机构信息

a Laboratory of Neuroendocrinology-Molecular Cell Physiology ; Institute of Pathophysiology ; Faculty of Medicine ; University of Ljubljana ; Ljubljana , Slovenia.

出版信息

Channels (Austin). 2015;9(2):96-101. doi: 10.1080/19336950.2015.1007825.

DOI:10.1080/19336950.2015.1007825
PMID:25835258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4595940/
Abstract

In regulated exocytosis vesicular and plasma membranes merge to form a fusion pore in response to stimulation. The nonselective cation HCN channels are involved in the regulation of unitary exocytotic events by at least 2 mechanisms. They can affect SNARE-dependent exocytotic activity indirectly, via the modulation of free intracellular calcium; and/or directly, by altering local cation concentration, which affects fusion pore geometry likely via electrostatic interactions. By monitoring membrane capacitance, we investigated how extracellular cation concentration affects fusion pore diameter in pituitary cells and astrocytes. At low extracellular divalent cation levels predominantly transient fusion events with widely open fusion pores were detected. However, fusion events with predominately narrow fusion pores were present at elevated levels of extracellular trivalent cations. These results show that electrostatic interactions likely help determine the stability of discrete fusion pore states by affecting fusion pore membrane composition.

摘要

在调节性胞吐作用中,囊泡膜和质膜响应刺激而融合形成融合孔。非选择性阳离子HCN通道至少通过两种机制参与单一胞吐事件的调节。它们可以通过调节细胞内游离钙间接影响依赖SNARE的胞吐活性;和/或直接通过改变局部阳离子浓度来影响,这可能通过静电相互作用影响融合孔的几何形状。通过监测膜电容,我们研究了细胞外阳离子浓度如何影响垂体细胞和星形胶质细胞中的融合孔直径。在低细胞外二价阳离子水平下,主要检测到具有广泛开放融合孔的短暂融合事件。然而,在细胞外三价阳离子水平升高时,存在主要具有狭窄融合孔的融合事件。这些结果表明,静电相互作用可能通过影响融合孔膜组成来帮助确定离散融合孔状态的稳定性。