细胞手性和生物系统对称性破坏的生物力学建模

Tasnif Rahman , Frank D. Peters , Leo Q. Wan
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引用次数: 0

摘要

越来越多的证据有力地表明,细胞手性在驱动左右对称破缺(LR)方面起着关键作用,而左右对称破缺是生物体内的一种普遍现象。整个胚胎和切除的器官历来被用来研究左右对称破缺,并取得了令人兴奋的发现。近年来,体外工程平台已成为揭示细胞手性偏向的有力工具,并揭示了手性形态发生的分子和生物物理观点,包括肌动蛋白细胞骨架的重要作用。在观察到的体内组织手性形态发生与确定的体外细胞手性偏向之间建立联系变得越来越重要。在这方面,计算数学模型具有巨大的价值,因为它们可以根据单个细胞的手性偏向来解释和预测组织的形态发生行为。在此,我们将介绍从分子和细胞水平到组织和器官水平等不同生物尺度的各种计算模型的建立和发现。此外,我们还深入探讨了此类模型在推进非对称细胞机械生物学研究中的未来方向和作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomechanical modeling of cell chirality and symmetry breaking of biological systems

Accumulating evidence strongly suggests that cell chirality plays a pivotal role in driving left-right (LR) symmetry breaking, a widespread phenomenon in living organisms. Whole embryos and excised organs have historically been employed to investigate LR symmetry breaking and have yielded exciting findings. In recent years, in vitro engineered platforms have emerged as powerful tools to reveal cellular chiral biases and led to uncovering molecular and biophysical insights into chiral morphogenesis, including the significant role of the actin cytoskeleton. Establishing a link between observed in vivo tissue chiral morphogenesis and the determined chiral bias of cells in vitro has become increasingly important. In this regard, computational mathematical models hold immense value as they can explain and predict tissue morphogenic behavior based on the chiral biases of individual cells. Here, we present the formulations and discoveries achieved using various computational models spanning different biological scales, from the molecular and cellular levels to tissue and organ levels. Furthermore, we offer insights into future directions and the role of such models in advancing the study of asymmetric cellular mechanobiology.

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