Dumont Sophie, Prakash Manu
Department of Cell and Tissue Biology and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94143-0512
Department of Bioengineering, Stanford University, Stanford, CA 94305-4125.
Mol Biol Cell. 2014 Nov 5;25(22):3461-5. doi: 10.1091/mbc.E14-03-0784.
Mechanical force organizes life at all scales, from molecules to cells and tissues. Although we have made remarkable progress unraveling the mechanics of life's individual building blocks, our understanding of how they give rise to the mechanics of larger-scale biological structures is still poor. Unlike the engineered macroscopic structures that we commonly build, biological structures are dynamic and self-organize: they sculpt themselves and change their own architecture, and they have structural building blocks that generate force and constantly come on and off. A description of such structures defies current traditional mechanical frameworks. It requires approaches that account for active force-generating parts and for the formation of spatial and temporal patterns utilizing a diverse array of building blocks. In this Perspective, we term this framework "emergent mechanics." Through examples at molecular, cellular, and tissue scales, we highlight challenges and opportunities in quantitatively understanding the emergent mechanics of biological structures and the need for new conceptual frameworks and experimental tools on the way ahead.
机械力在从分子到细胞和组织的所有尺度上构建生命。尽管我们在揭示生命个体组成部分的力学原理方面取得了显著进展,但我们对这些组成部分如何产生更大尺度生物结构的力学原理的理解仍然不足。与我们通常构建的工程宏观结构不同,生物结构是动态且自组织的:它们塑造自身并改变自身结构,并且它们具有能够产生力且不断开启和关闭的结构组成部分。对这类结构的描述超出了当前传统力学框架的范畴。它需要考虑主动产生力的部分以及利用各种组成部分形成空间和时间模式的方法。在这篇观点文章中,我们将这个框架称为“涌现力学”。通过分子、细胞和组织尺度的实例,我们强调了在定量理解生物结构的涌现力学方面所面临的挑战和机遇,以及在未来道路上对新的概念框架和实验工具的需求。