Suppr超能文献

突触囊泡在被募集到易释放池中后的超级引发。

Superpriming of synaptic vesicles after their recruitment to the readily releasable pool.

机构信息

Cell Physiology Laboratory, Department of Physiology and Bio-Membrane Plasticity Research Center, Seoul National University College of Medicine and Neuroscience Research Institute, Seoul National University Medical Research Center, Seoul 110-799, Republic of Korea.

出版信息

Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):15079-84. doi: 10.1073/pnas.1314427110. Epub 2013 Aug 26.

Abstract

Recruitment of release-competent vesicles during sustained synaptic activity is one of the major factors governing short-term plasticity. During bursts of synaptic activity, vesicles are recruited to a fast-releasing pool from a reluctant vesicle pool through an actin-dependent mechanism. We now show that newly recruited vesicles in the fast-releasing pool do not respond at full speed to a strong Ca(2+) stimulus, but require approximately 4 s to mature to a "superprimed" state. Superpriming was found to be altered by agents that modulate the function of unc13 homolog proteins (Munc13s), but not by calmodulin inhibitors or actin-disrupting agents. These findings indicate that recruitment and superpriming of vesicles are regulated by separate mechanisms, which require integrity of the cytoskeleton and activation of Munc13s, respectively. We propose that refilling of the fast-releasing vesicle pool proceeds in two steps, rapid actin-dependent "positional priming," which brings vesicles closer to Ca(2+) sources, followed by slower superpriming, which enhances the Ca(2+) sensitivity of primed vesicles.

摘要

在持续的突触活动期间,释放能力的囊泡的募集是控制短期可塑性的主要因素之一。在突触活动的爆发期间,囊泡通过肌动蛋白依赖性机制从不情愿的囊泡池中募集到快速释放池。现在我们表明,快速释放池中新募集的囊泡不会以全速响应强 Ca(2+)刺激,而是需要大约 4 秒才能成熟到“超级引发”状态。发现超级引发会被调节 unc13 同源蛋白 (Munc13s) 功能的试剂改变,但不会被钙调蛋白抑制剂或肌动蛋白破坏剂改变。这些发现表明囊泡的募集和超级引发是由不同的机制调节的,分别需要细胞骨架的完整性和 Munc13s 的激活。我们提出,快速释放囊泡池的再填充分两步进行,快速肌动蛋白依赖性“位置引发”,使囊泡更接近 Ca(2+)源,然后是较慢的超级引发,增强引发囊泡的 Ca(2+)敏感性。

相似文献

1
Superpriming of synaptic vesicles after their recruitment to the readily releasable pool.突触囊泡在被募集到易释放池中后的超级引发。
Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):15079-84. doi: 10.1073/pnas.1314427110. Epub 2013 Aug 26.
5
Apparent calcium dependence of vesicle recruitment.囊泡募集的明显钙依赖性。
J Physiol. 2018 Oct;596(19):4693-4707. doi: 10.1113/JP275911. Epub 2018 Aug 7.
9
Quantitative analysis of vesicle recycling at the calyx of Held synapse.对海氏壶腹突触处囊泡循环的定量分析。
Proc Natl Acad Sci U S A. 2015 Apr 14;112(15):4779-84. doi: 10.1073/pnas.1424597112. Epub 2015 Mar 30.

引用本文的文献

3
Synapse-specific catecholaminergic modulation of neuronal glutamate release.神经元谷氨酸释放的突触特异性儿茶酚胺能调节
Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2420496121. doi: 10.1073/pnas.2420496121. Epub 2024 Dec 30.
4
Exact Distribution of the Quantal Content in Synaptic Transmission.突触传递中量子含量的确切分布。
Phys Rev Lett. 2024 May 31;132(22):228401. doi: 10.1103/PhysRevLett.132.228401.
9
SNARE Proteins in Synaptic Vesicle Fusion.突触小泡融合中的 SNARE 蛋白。
Adv Neurobiol. 2023;33:63-118. doi: 10.1007/978-3-031-34229-5_4.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验