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根据钙扩散模型模拟计算得出的递质释放时间进程。

Time course of transmitter release calculated from simulations of a calcium diffusion model.

作者信息

Yamada W M, Zucker R S

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720.

出版信息

Biophys J. 1992 Mar;61(3):671-82. doi: 10.1016/S0006-3495(92)81872-6.

Abstract

A three-dimensional presynaptic calcium diffusion model developed to account for characteristics of transmitter release was modified to provide for binding of calcium to a receptor and subsequent triggering of exocytosis. When low affinity (20 microM) and rapid kinetics were assumed for the calcium receptor triggering exocytosis, and stimulus parameters were selected to match those of experiments, the simulations predicted a virtual invariance of the time course of transmitter release to paired stimulation, stimulation with pulses of different amplitude, and stimulation in different calcium solutions. The large temperature sensitivity of experimental release time course was explained by a temperature sensitivity of the model's final rate limiting exocytotic process. Inclusion of calcium tail currents and a saturable buffer with finite binding kinetics resulted in high peak calcium transients near release sites, exceeding 100 microM. Models with a single class of calcium binding site to the secretory trigger molecule failed to produce sufficient synaptic facilitation under this condition. When at least one calcium ion binds to a different site having higher affinity and slow kinetics, facilitation again reaches levels similar to those seen experimentally. It is possible that the neurosecretory trigger molecule reacts with calcium at more than one class of binding site.

摘要

为解释递质释放的特征而建立的三维突触前钙扩散模型进行了修改,以考虑钙与受体的结合以及随后的胞吐触发。当假定触发胞吐的钙受体具有低亲和力(20微摩尔)和快速动力学,并且选择刺激参数以匹配实验参数时,模拟预测递质释放的时间进程对于配对刺激、不同幅度脉冲刺激以及在不同钙溶液中的刺激几乎不变。实验释放时间进程的较大温度敏感性由模型最终限速胞吐过程的温度敏感性来解释。包含钙尾电流和具有有限结合动力学的可饱和缓冲液导致释放位点附近出现高峰钙瞬变,超过100微摩尔。在这种情况下,具有一类与分泌触发分子结合的钙结合位点的模型无法产生足够的突触易化。当至少一个钙离子与具有更高亲和力和慢动力学的不同位点结合时,易化作用再次达到与实验观察到的水平相似的程度。神经分泌触发分子有可能在不止一类结合位点与钙发生反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c50b/1260285/1945318f710f/biophysj00104-0085-a.jpg

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