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引用次数: 0
摘要
减小了两个最长打开状态的时间常数,降低了最终关闭状态和初始打开状态之间的转换效率。这些结果表明,辅助亚基可以影响GABA A R的单通道特性。具体来说,Shisa7改变了GABA A R通道在爆发时的门控动力学。这一效应解释了在之前的全细胞记录中测量的GABA A Rs的加速失活动力学。结合先前的研究表明Shisa7促进GABA A Rs的表面表达,本研究表明Shisa7通过使全细胞GABA电流振幅更大,持续时间更短来塑造神经元的抑制性输入。这可能对调节尖峰时间很重要。
decreased the time constants of the two longest open states, and reduced the efficacy of transitions between the final closed state and the initial open state. These results demonstrate that auxiliary subunits can affect single-channel properties of GABA A Rs. Specifically, Shisa7 alters the kinetics of GABA A R channel gating during bursts. This effect explains the accelerated deactivation kinetics of GABA A Rs measured in previous whole-cell recordings. Together with previous work showing Shisa7 pro-motes surface expression of GABA A Rs, this study suggests that Shisa7 shapes inhibitory input to neurons by making whole-cell GABA currents larger in amplitude, but shorter in duration. This might be impor-tant for regulating spike timing.