Wang Xueyong, Engisch Kathrin L, Li Yingjie, Pinter Martin J, Cope Timothy C, Rich Mark M
Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Neurosci. 2004 Nov 24;24(47):10687-92. doi: 10.1523/JNEUROSCI.2755-04.2004.
We examined the mechanism underlying increased quantal content after block of activity at the mouse neuromuscular junction in vivo. We found that, when quantal content was measured in solution containing normal extracellular calcium, block of activity had no effect on either quantal content or the response to repetitive stimulation. However, when quantal content was measured in low extracellular calcium, there was a large increase in quantal content after block of activity. The increase in quantal content was accompanied by increased depression during repetitive stimulation. The explanation for these findings was that there was a shift in the calcium dependence of release after block of activity that manifested as an increase in probability of release in low extracellular calcium. Block of presynaptic P/Q channels eliminated the increase in probability of release. We propose that activity-dependent regulation of presynaptic calcium entry may contribute to homeostatic regulation of quantal content.
我们研究了在体内阻断小鼠神经肌肉接头处的活动后量子含量增加的潜在机制。我们发现,当在含有正常细胞外钙的溶液中测量量子含量时,阻断活动对量子含量或对重复刺激的反应均无影响。然而,当在低细胞外钙中测量量子含量时,阻断活动后量子含量大幅增加。量子含量的增加伴随着重复刺激期间抑制作用的增强。这些发现的解释是,阻断活动后释放的钙依赖性发生了转变,表现为在低细胞外钙中释放概率增加。阻断突触前P/Q通道消除了释放概率的增加。我们提出,突触前钙内流的活动依赖性调节可能有助于量子含量的稳态调节。