Nucleation feedback can drive establishment and maintenance of biased microtubule polarity in neurites

IF 1.8 4区 数学 Q2 BIOLOGY
Hannah G. Scanlon , Gibarni Mahata , Anna C. Nelson , Scott A. McKinley , Melissa M. Rolls , Maria-Veronica Ciocanel
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引用次数: 0

Abstract

The microtubule cytoskeleton is comprised of dynamic, polarized filaments that facilitate transport within the cell. Polarized microtubule arrays are key to facilitating cargo transport in long cells such as neurons. Microtubules also undergo dynamic instability, where the plus and minus ends of the filaments switch between growth and shrinking phases, leading to frequent microtubule turnover. Although microtubules often completely disassemble and new filaments nucleate, microtubule arrays have been observed to both maintain their biased orientation throughout the cell lifetime and to rearrange their polarity as an adaptive response to injury. Motivated by cytoskeleton organization in neurites, we propose a spatially-explicit stochastic model of microtubule arrays and investigate how nucleation of new filaments could generate biased polarity in a simple linear domain. Using a continuous-time Markov chain model of microtubule growth dynamics, we model and parameterize two experimentally-validated nucleation mechanisms: nucleation feedback, where the direction of filament growth depends on existing microtubule content, and a checkpoint mechanism, where microtubules that nucleate in a direction opposite to the majority experience frequent catastrophe. When incorporating these validated mechanisms into the spatial model, we find that nucleation feedback is sufficient to establish biased polarity in neurites of different lengths, and that the emergence and maintenance of biased polarity is relatively stable in spite of stochastic fluctuations. This work provides a framework to study the relationship between microtubule nucleation and polarity, and could extend to give insights into mechanisms that drive the formation of polarized filament arrays in other biological settings.
成核反馈可以驱动神经突中偏置微管极性的建立和维持。
微管细胞骨架由动态的极化细丝组成,促进细胞内的运输。极化微管阵列是促进长细胞(如神经元)中货物运输的关键。微管也经历动态不稳定性,其中细丝的正负端在生长和收缩阶段之间切换,导致频繁的微管周转。尽管微管经常完全解体,新的细丝形成核,但已经观察到微管阵列在整个细胞寿命中都保持其偏向性取向,并且作为对损伤的适应性反应重新排列其极性。在神经突细胞骨架组织的激励下,我们提出了一个空间明确的微管阵列随机模型,并研究了新细丝的成核如何在简单的线性域内产生偏极性。利用微管生长动力学的连续时间马尔可夫链模型,我们模拟并参数化了两种实验验证的成核机制:成核反馈机制,其中丝的生长方向取决于现有的微管含量;以及检查点机制,其中与大多数方向相反的微管经常发生突变。当将这些验证的机制纳入空间模型时,我们发现成核反馈足以在不同长度的神经突中建立偏极性,并且尽管有随机波动,偏极性的出现和维持是相对稳定的。这项工作为研究微管成核和极性之间的关系提供了一个框架,并可以扩展到深入了解在其他生物环境中驱动极化灯丝阵列形成的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mathematical Biosciences
Mathematical Biosciences 生物-生物学
CiteScore
7.50
自引率
2.30%
发文量
67
审稿时长
18 days
期刊介绍: Mathematical Biosciences publishes work providing new concepts or new understanding of biological systems using mathematical models, or methodological articles likely to find application to multiple biological systems. Papers are expected to present a major research finding of broad significance for the biological sciences, or mathematical biology. Mathematical Biosciences welcomes original research articles, letters, reviews and perspectives.
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