Two-dimensional interfacial diffusion model of inhibitory synaptic receptor dynamics

被引:5
作者
Bressloff, Paul. C. C. [1 ]
机构
[1] Univ Utah, Dept Math, 155 South 1400 East, Salt Lake City, UT 84112 USA
来源
PROCEEDINGS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2023年 / 479卷 / 2274期
关键词
diffusion; semi-permeable membranes; liquid-liquid phase separation; synapses; 1ST PASSAGE TIME; GLYCINE RECEPTORS; AMPA RECEPTORS; SURFACE TRAFFICKING; ORGANIZATION; MEMBRANE; PLASTICITY;
D O I
10.1098/rspa.2022.0831
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The diffusion-trapping of protein receptors in post-synaptic regions of a neuron's plasma membrane plays a key role in determining the strength of synaptic connections and their regulation during learning and memory. In this paper, we construct and analyse a two-dimensional interfacial diffusion model of inhibitory synaptic receptor dynamics. The model involves three major components. First, the boundary of each synapse is treated as a semi-permeable interface due to the effects of cytoskeletal structures. Second, the effective diffusivity within a synapse is taken to be smaller than the extrasynaptic diffusivity due to the temporary binding to scaffold protein buffers within the synapse. Third, receptors from intracellular pools are inserted into the membrane extrasynaptically and internalized extrasynaptically and synaptically. We first solve the model equations for a single synapse in an unbounded domain and explore how the non-equilibrium steady-state number of synaptic receptors depends on model parameters including synaptic radius and the permeability of the synaptic interface. We then use matched asymptotic analysis to solve the corresponding problem of multiple synapses in a large, bounded domain. In particular, we show how diffusion mediates pairwise synaptic interactions that could provide a substrate for heterosynaptic plasticity. Finally, we indicate how to apply the model to the stochastic dynamics of single receptors.
引用
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页数:19
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