论文标题
抑制性突触受体动力学的2D界面扩散模型
2D interfacial diffusion model of inhibitory synaptic receptor dynamics
论文作者
论文摘要
神经元突触后膜内蛋白受体的横向扩散和捕获在确定突触连接的强度及其在学习和记忆过程中的调节方面起着关键作用。在本文中,我们构建和分析了抑制性突触受体动力学的2D界面扩散模型。该模型涉及三个主要组成部分。首先,由于细胞骨架结构的影响,每个突触的边界被视为半渗透界面。其次,由于突触中的暂时结合与突触中的脚手架蛋白缓冲液的暂时结合,突触中的有效扩散率小于突触外扩散率。第三,细胞内池的受体被插入膜外突触和内在的突触外和突触。我们首先在无界域中求解单个突触的模型方程,并探讨非平衡稳态数量的突触受体数量如何取决于模型参数。然后,我们使用匹配的渐近分析来解决大型,有界域中多个突触的相应问题。最后,将突触视为脚手架蛋白的相分离的冷凝物,我们描述了如何以界面扩散来建模单个支架蛋白的扩散。因此,我们建立了界面扩散,作为探索突触动力学和可塑性的一般范式。
The lateral diffusion and trapping of protein receptors within the postsynaptic membrane of a neuron plays a key role in determining the strength of synaptic connections and their regulation during learning and memory. In this paper we construct and analyze a 2D 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. We then use matched asymptotic analysis to solve the corresponding problem of multiple synapses in a large, bounded domain. Finally, treating a synapse as a phase separated condensate of scaffold proteins, we describe how diffusion of individual scaffold proteins can also be modeled in terms of interfacial diffusion. We thus establish interfacial diffusion as a general paradigm for exploring synaptic dynamics and plasticity.