Nelson Celeste M, Jean Ronald P, Tan John L, Liu Wendy F, Sniadecki Nathan J, Spector Alexander A, Chen Christopher S
Department of Biomedical Engineering, The Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11594-9. doi: 10.1073/pnas.0502575102. Epub 2005 Jul 27.
Spatial patterns of cellular growth generate mechanical stresses that help to push, fold, expand, and deform tissues into their specific forms. Genetic factors are thought to specify patterns of growth and other behaviors to drive morphogenesis. Here, we show that tissue form itself can feed back to regulate patterns of proliferation. Using micro-fabrication to control the organization of sheets of cells, we demonstrated the emergence of stable patterns of proliferative foci. Regions of concentrated growth corresponded to regions of high tractional stress generated within the sheet, as predicted by a finite-element model of multicellular mechanics and measured directly by using a micromechanical force sensor array. Inhibiting actomyosin-based tension or cadherin-mediated connections between cells disrupted the spatial pattern of proliferation. These findings demonstrate the existence of patterns of mechanical forces that originate from the contraction of cells, emerge from their multicellular organization, and result in patterns of growth. Thus, tissue form is not only a consequence but also an active regulator of tissue growth.
细胞生长的空间模式会产生机械应力,这些应力有助于推动、折叠、扩展组织并使其变形为特定形态。遗传因素被认为决定了生长模式和其他行为以驱动形态发生。在此,我们表明组织形态本身可以反馈调节增殖模式。通过微加工来控制细胞片层的组织,我们证明了增殖灶稳定模式的出现。如多细胞力学有限元模型所预测并通过微机械力传感器阵列直接测量的那样,集中生长区域对应于细胞片层内产生的高牵引应力区域。抑制基于肌动球蛋白的张力或细胞间钙黏蛋白介导的连接会破坏增殖的空间模式。这些发现证明了存在源于细胞收缩、从其多细胞组织中出现并导致生长模式的机械力模式。因此,组织形态不仅是组织生长的结果,也是其主动调节因子。