Cell-cycle control by physiological matrix elasticity and in vivo tissue stiffening

Background—A number of adhesion-mediated signaling pathways and cell cycle events have been identified that regulate cell proliferation, yet studies to date have been unable to determine which of these pathways control mitogenesis in response to physiologically relevant changes in tissue elasticity. In this report, we have used hydrogel-based substrata matched to biological tissue stiffness to investigate the effects of matrix elasticity on the cell cycle. Results—We find that physiological tissue stiffness acts as a cell cycle inhibitor in mammary epithelial cells and vascular smooth muscle cells; subcellular analysis in these cells, mouse embryo fibroblasts, and osteoblasts shows that cell cycle control by matrix stiffness is widely conserved. Remarkably, most mitogenic events previously documented as ECM/integrin-dependent proceed normally when matrix stiffness is altered in the range that controls mitogenesis. These include ERK activity, immediately-early gene expression, and cdk inhibitor expression. In contrast, FAK-dependent Rac activation, Rac-dependent cyclin D1 gene induction, and cyclin D1-dependent Rb phosphorylation are strongly inhibited at physiological tissue stiffness and rescued when the matrix is stiffened in vitro. Importantly, the combined use of atomic force microscopy and fluorescence imaging in the mouse shows that comparable increases in tissue stiffness occur at sites of cell proliferation in vivo. Conclusion—Matrix remodeling associated with pathogenesis is, in itself, a positive regulator of the cell cycle through a highly selective effect on integrin-dependent signaling to FAK, Rac, and cyclin D1