Physics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.
Group for Computational Life Sciences, Division of Physical Chemistry, Ruđer Bošković Institute, Zagreb 10000, Croatia.
Proc Natl Acad Sci U S A. 2024 Nov 5;121(45):e2308126121. doi: 10.1073/pnas.2308126121. Epub 2024 Oct 28.
Despite the primary role of cell proliferation in tissue development and homeostatic maintenance, the interplay between cell density, cell mechanoresponse, and cell growth and division is not yet understood. In this article, we address this issue by reporting on an experimental investigation of cell proliferation on all time- and length-scales of the development of a model tissue, grown on collagen-coated glass or deformable substrates. Through extensive data analysis, we demonstrate the relation between mechanoresponse and probability for cell division, as a function of the local cell density. Motivated by these results, we construct a minimal model of cell division in tissue environment that can recover the data. By parameterizing the growth and the dividing phases of the cell cycle, and introducing such a proliferation model in dissipative particle dynamics simulations, we recover the mechanoresponsive, time-dependent density profiles in 2D tissues growing to macroscopic scales. The importance of separating the cell population into growing and dividing cells, each characterized by a particular time scale, is further emphasized by calculations of density profiles based on adapted Fisher-Kolmogorov equations. Together, these results show that the mechanoresponse on the level of a constitutive cell and its proliferation results in a matrix-sensitive active pressure. The latter evokes massive cooperative displacement of cells in the invading tissue and is a key factor for developing large-scale structures in the steady state.
尽管细胞增殖在组织发育和动态平衡维持中起着主要作用,但细胞密度、细胞力学响应、细胞生长和分裂之间的相互作用还没有被理解。在本文中,我们通过报告在胶原蛋白涂覆的玻璃或可变形基底上生长的模型组织的发育的所有时间和长度尺度上的细胞增殖的实验研究来解决这个问题。通过广泛的数据分析,我们展示了力学响应与细胞分裂概率之间的关系,作为局部细胞密度的函数。受这些结果的启发,我们构建了一个细胞分裂的最小模型,该模型可以恢复数据。通过对细胞周期的生长和分裂阶段进行参数化,并在耗散粒子动力学模拟中引入这种增殖模型,我们在生长到宏观尺度的二维组织中恢复了力学响应的、时变的密度分布。通过基于适应性 Fisher-Kolmogorov 方程的密度分布计算,进一步强调了将细胞群体分为生长细胞和分裂细胞的重要性,每个细胞都有特定的时间尺度。总之,这些结果表明,在组成型细胞的水平上的力学响应及其增殖导致了对基质敏感的主动压力。后者在入侵组织中引发大量的细胞协同位移,是在稳态中形成大尺度结构的关键因素。