Mode switching of Inositol 1,4,5-trisphosphate receptor channel shapes the Spatiotemporal scales of Ca(2+) signals

肌醇1,4,5-三磷酸受体通道的模式转换塑造了Ca(2+)信号的时空尺度

阅读:1

Abstract

The inositol 1,4,5-trisphosphate (InsP(3)) receptor (InsP(3)R) channel is crucial for the generation and modulation of highly specific intracellular Ca(2+) signals performing numerous functions in animal cells. However, the single channel behavior during Ca(2+) signals of different spatiotemporal scales is not well understood. To elucidate the correlation between the gating dynamics of single InsP(3)Rs and spatiotemporal Ca(2+) patterns, we simulate a cluster of InsP(3)Rs under varying ligand concentrations and extract comprehensive gating statistics of all channels during events of different sizes and durations. Our results show that channels gating predominantly in the low activity mode with negligible occupancy of intermediate and high modes leads to single channel Ca(2+) release event blips. Increasing occupancies of intermediate and high modes results in events with increasing size. When the channel has more than 50% probability of gating in the intermediate and high modes, the cluster generates very large puffs that would most likely result in global Ca(2+) signals. The size, duration and frequency of Ca(2+) signals all increase linearly with the total probability of channel gating in the intermediate and high modes. To our knowledge, this is the first study that quantitatively relates the modal characteristics of InsP(3)R to the shaping of different spatiotemporal scales of Ca(2+) signals.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。