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胆固醇在突触小泡肿胀中的作用。

Involvement of cholesterol in synaptic vesicle swelling.

机构信息

Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

Exp Biol Med (Maywood). 2010 Apr;235(4):470-7. doi: 10.1258/ebm.2010.009259.

DOI:10.1258/ebm.2010.009259
PMID:20407079
Abstract

Studies demonstrate that cholesterol plays a critical role in the regulation of neurotransmitter release and that secretory vesicle swelling is a requirement for the regulated expulsion of intravesicular contents during cell secretion. In view of this, the involvement of cholesterol in synaptic vesicle swelling was hypothesized and tested in the present study, using isolated synaptic vesicles from rat brain and the determination of their swelling competency in the presence and absence of cholesterol. The involvement of the water channel aquaporin-6 (AQP-6) and proton pump vH(+)-ATPase in GTP-G(alpha o)-mediated synaptic vesicle swelling has been reported previously. Mastoparan, the amphiphilic tetradecapeptide from wasp venom, known to activate the GTPase activity of G(alpha o/i) proteins, stimulates synaptic vesicle swelling in the presence of GTP. In the current study, using nanometer-scale precision measurements of isolated synaptic vesicles, we report for the first time that depletion of cholesterol from synaptic vesicle membrane results in a significant loss of GTP-mastoparan-stimulable synaptic vesicle swelling. In contrast, incorporation of cholesterol into the synaptic vesicle membrane potentiates GTP-mastoparan-stimulable vesicle swelling. Our study further demonstrates that this effect of cholesterol is due, in part, to its involvement in the interactions between AQP-6, vH(+)-ATPase and the GTP-binding G(alpha o) protein at the synaptic vesicle membrane.

摘要

研究表明,胆固醇在神经递质释放的调节中起着关键作用,而分泌小泡的肿胀是细胞分泌过程中囊内物质有规律排出的必要条件。有鉴于此,本研究假设胆固醇参与突触小泡肿胀,并在存在和不存在胆固醇的情况下,用大鼠脑分离的突触小泡来测定其肿胀能力。水通道 Aquaporin-6(AQP-6)和质子泵 vH(+)-ATPase 参与 GTP-G(alpha o)介导的突触小泡肿胀,这一点先前已有报道。蜂毒中的两性十四肽 Mastoparan 已知能激活 G(alpha o/i)蛋白的 GTPase 活性,在 GTP 存在的情况下刺激突触小泡肿胀。在本研究中,我们使用纳米级精度的分离突触小泡进行测量,首次报道了从突触小泡膜中去除胆固醇会导致 GTP-Mastoparan 刺激的突触小泡肿胀明显丧失。相比之下,将胆固醇掺入突触小泡膜中会增强 GTP-Mastoparan 刺激的囊泡肿胀。我们的研究进一步表明,胆固醇的这种作用部分是由于其参与了突触小泡膜上 AQP-6、vH(+)-ATPase 和与 GTP 结合的 G(alpha o)蛋白之间的相互作用。

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