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