Emergence of Form from Function - Mechanical Engineering Approaches to Probe the Role of Stem Cell Mechanoadaptation in Sealing Cell Fate.

Bioarchitecture Pub Date : 2016-01-01 Epub Date: 2016-10-14 DOI:10.1080/19490992.2016.1229729
Melissa L Knothe Tate, Peter W Gunning, Vittorio Sansalone
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引用次数: 15

Abstract

Stem cell "mechanomics" refers to the effect of mechanical cues on stem cell and matrix biology, where cell shape and fate are intrinsic manifestations of form and function. Before specialization, the stem cell itself serves as a sensor and actuator; its structure emerges from its local mechanical milieu as the cell adapts over time. Coupling of novel spatiotemporal imaging and computational methods allows for linking of the energy of adaptation to the structure, biology and mechanical function of the cell. Cutting edge imaging methods enable probing of mechanisms by which stem cells' emergent anisotropic architecture and fate commitment occurs. A novel cell-scale model provides a mechanistic framework to describe stem cell growth and remodeling through mechanical feedback; making use of a generalized virtual power principle, the model accounts for the rate of doing work or the rate of using energy to effect the work. This coupled approach provides a basis to elucidate mechanisms underlying the stem cell's innate capacity to adapt to mechanical stimuli as well as the role of mechanoadaptation in lineage commitment. An understanding of stem cell mechanoadaptation is key to deciphering lineage commitment, during prenatal development, postnatal wound healing, and engineering of tissues.

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从功能中产生形态——用机械工程方法探讨干细胞机械适应在封闭细胞命运中的作用。
干细胞“机械组学”是指机械线索对干细胞和基质生物学的影响,其中细胞的形状和命运是形式和功能的内在表现。在分化之前,干细胞本身充当传感器和执行器;随着细胞适应时间的推移,其结构从其局部机械环境中产生。新的时空成像和计算方法的耦合允许将适应能量与细胞的结构,生物学和机械功能联系起来。尖端的成像方法能够探测干细胞涌现的各向异性结构和命运承诺发生的机制。一个新的细胞尺度模型提供了一个机制框架来描述干细胞的生长和重塑通过机械反馈;该模型利用广义虚功率原理,计算了做功速率或做功所用能量的速率。这种耦合方法为阐明干细胞适应机械刺激的先天能力的机制以及机械适应在谱系承诺中的作用提供了基础。了解干细胞的机制适应是破译谱系承诺、产前发育、产后伤口愈合和组织工程的关键。
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Letter from the editors. The impact of tropomyosins on actin filament assembly is isoform specific. Geometric control and modeling of genome reprogramming. Post-polymerization crosstalk between the actin cytoskeleton and microtubule network. Where are the limits of the centrosome?
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