Junge Harald J, Rhee Jeong-Seop, Jahn Olaf, Varoqueaux Frederique, Spiess Joachim, Waxham M Neal, Rosenmund Christian, Brose Nils
Department of Molecular Neurobiology, Max-Planck-Institute for Experimental Medicine, Hermann-Rein-Strasse 3, D-37077 Göttingen, Germany.
Cell. 2004 Aug 6;118(3):389-401. doi: 10.1016/j.cell.2004.06.029.
The efficacy of synaptic transmission between neurons can be altered transiently during neuronal network activity. This phenomenon of short-term plasticity is a key determinant of network properties; is involved in many physiological processes such as motor control, sound localization, or sensory adaptation; and is critically dependent on cytosolic [Ca2+]. However, the underlying molecular mechanisms and the identity of the Ca2+ sensor/effector complexes involved are unclear. We now identify a conserved calmodulin binding site in UNC-13/Munc13s, which are essential regulators of synaptic vesicle priming and synaptic efficacy. Ca2+ sensor/effector complexes consisting of calmodulin and Munc13s regulate synaptic vesicle priming and synaptic efficacy in response to a residual [Ca2+] signal and thus shape short-term plasticity characteristics during periods of sustained synaptic activity.
在神经网络活动期间,神经元之间突触传递的效能可被短暂改变。这种短期可塑性现象是网络特性的关键决定因素;参与许多生理过程,如运动控制、声音定位或感觉适应;并且严重依赖于胞质[Ca2+]。然而,其潜在的分子机制以及所涉及的Ca2+传感器/效应器复合物的身份尚不清楚。我们现在在UNC-13/Munc13s中鉴定出一个保守的钙调蛋白结合位点,UNC-13/Munc13s是突触小泡启动和突触效能的重要调节因子。由钙调蛋白和Munc13s组成的Ca2+传感器/效应器复合物响应残余的[Ca2+]信号调节突触小泡启动和突触效能,从而在持续突触活动期间塑造短期可塑性特征。