轴突运输的排队模型

Q3 Engineering Brain multiphysics Pub Date : 2021-01-01 DOI:10.1016/j.brain.2021.100042
Paul C. Bressloff
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引用次数: 5

摘要

运动驱动的囊泡细胞内转运到神经元轴突和树突的突触靶点,在正常细胞功能中起着至关重要的作用。此外,主动转运的刺激依赖性调节是长期突触可塑性的重要组成部分,而囊泡转运的破坏可导致各种神经退行性疾病的发生。在本文中,我们研究了轴突中囊泡运输的离散性和随机性如何影响突触目标内资源积累的波动。我们首先解决单个马达-货物复合体(粒子)寻找沿一维轴突电缆分布的突触目标的第一次通过时间问题。然后,我们使用排队理论分析了在多个搜索捕获事件和退化的联合作用下突触资源的积累。特别是,我们确定了响应周期性粒子插入的突触资源沿轴突分布的稳态均值和方差。平均分布恢复了确定性人口模型中常见的资源的空间衰减分布。然而,囊泡运输的离散性可能导致Fano因子在突触阵列上大于统一(非泊松),从而导致显著的波动爆发。我们还发现,每个突触Fano因子与颗粒插入率无关,但随着每个囊泡中蛋白质货物的数量单调增加。这意味着波动可以通过增加注射速度同时减少每个囊泡的载货量来减小。运动驱动的囊泡细胞内转运到神经元轴突和树突的突触靶点在正常细胞功能中起着至关重要的作用。此外,主动转运的刺激依赖性调节是长期突触可塑性的重要组成部分,而囊泡转运的破坏可导致各种神经退行性疾病的发生。在本文中,我们研究了轴突中囊泡运输的离散性和随机性如何影响突触目标内资源积累的波动。几乎所有先前的轴突运输研究都集中在确定性种群模型上,或者单个运动粒子寻找目标的随机模型上。本文的新颖之处在于采用了以目标为中心的观点,关注了多个搜索捕获事件下突触目标内资源的积累。特别是,在作者先前关于基于细胞素的形态发生的工作的基础上,他开发了一个基于排队论的研究突触资源积累的一般框架。本文的两个主要结果如下:(i)囊泡运输的离散性可能导致突触阵列上的Fano因子大于统一(非泊松),从而导致显著的波动爆发。(ii)每个突触Fano因子与颗粒插入率无关,但随着每个囊泡中蛋白质载货量的增加而单调增加。这意味着波动可以通过增加注射速度同时减少每个囊泡的载货量来减小。在讨论中强调了基本模型的广泛可能的扩展。
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Queuing model of axonal transport

The motor-driven intracellular transport of vesicles to synaptic targets in the axons and dendrites of neurons plays a crucial role in normal cell function. Moreover, stimulus-dependent regulation of active transport is an important component of long-term synaptic plasticity, whereas the disruption of vesicular transport can lead to the onset of various neurodegenerative diseases. In this paper we investigate how the discrete and stochastic nature of vesicular transport in axons contributes to fluctuations in the accumulation of resources within synaptic targets. We begin by solving the first passage time problem of a single motor-cargo complex (particle) searching for synaptic targets distributed along a one-dimensional axonal cable. We then use queuing theory to analyze the accumulation of synaptic resources under the combined effects of multiple search-and-capture events and degradation. In particular, we determine the steady-state mean and variance of the distribution of synaptic resources along the axon in response to the periodic insertion of particles. The mean distribution recovers the spatially decaying distribution of resources familiar from deterministic population models. However, the discrete nature of vesicular transport can lead to Fano factors that are greater than unity (non-Poissonian) across the array of synapses, resulting in significant fluctuation bursts. We also find that each synaptic Fano factor is independent of the rate of particle insertion but increases monotonically with the amount of protein cargo in each vesicle. This implies that fluctuations can be reduced by increasing the injection rate while decreasing the cargo load of each vesicle.

Statement of Significance

The motor-driven intracellular transport of vesicles to synaptic targets in the axons and dendrites of neurons plays a crucial role in normal cell function. Moreover, stimulus-dependent regulation of active transport is an important component of long-term synaptic plasticity, whereas the disruption of vesicular transport can lead to the onset of various neurodegenerative diseases. In this paper we investigate how the discrete and stochastic nature of vesicular transport in axons contributes to fluctuations in the accumulation of resources within synaptic targets. Almost all previous studies of axonal transport have focused on deterministic population models, or on stochastic models of a single motor particle searching for a target. The novel feature of the current paper is to take a target-centric viewpoint, which focuses on the accumulation of resources within synaptic targets under multiple search-and-capture events. In particular, building on previous work by the author on cytoneme-based morphogenesis, he develops a general framework for studying synaptic resource accumulation based on queuing theory. Two major results of the paper are as follows: (i) the discrete nature of vesicular transport can lead to Fano factors that are greater than unity (non-Poissonian) across the array of synapses, resulting in significant fluctuation bursts. (ii) Each synaptic Fano factor is independent of the rate of particle insertion but increases monotonically with the amount of protein cargo in each vesicle. This implies that fluctuations can be reduced by increasing the injection rate while decreasing the cargo load of each vesicle. A wide range of possible extensions of the basic model are highlighted in the discussion.

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来源期刊
Brain multiphysics
Brain multiphysics Physics and Astronomy (General), Modelling and Simulation, Neuroscience (General), Biomedical Engineering
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
68 days
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