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Breast epithelial cells sense the stiffness of the extracellular matrix through Rho-mediated contractility. In turn, matrix stiffness regulates RhoA activity. However, the upstream signaling mechanisms are poorly defined. Here we demonstrate that the Rho exchange factor GEF-H1 mediates RhoA activation in response to extracellular matrix stiffness. We demonstrate the novel finding that microtubule stability is diminished by a stiff three-dimensional (3D) extracellular matrix, which leads to the activation of GEF-H1. Surprisingly, activation of the mitogen-activated protein kinase kinase/extracellular signal-regulated kinase pathway did not contribute to stiffness-induced GEF-H1 activation. Loss of GEF-H1 decreases cell contraction of and invasion through 3D matrices. These data support a model in which matrix stiffness regulates RhoA through microtubule destabilization and the subsequent release and activation of GEF-H1.
MAP Kinase Signaling System, Protein Stability, Epithelial Cells, Articles, Microtubules, Biomechanical Phenomena, Extracellular Matrix, Mice, Mammary Glands, Animal, Cell Movement, Gene Knockdown Techniques, Animals, Guanine Nucleotide Exchange Factors, Humans, RNA Interference, Extracellular Signal-Regulated MAP Kinases, rhoA GTP-Binding Protein, Cells, Cultured, Rho Guanine Nucleotide Exchange Factors
MAP Kinase Signaling System, Protein Stability, Epithelial Cells, Articles, Microtubules, Biomechanical Phenomena, Extracellular Matrix, Mice, Mammary Glands, Animal, Cell Movement, Gene Knockdown Techniques, Animals, Guanine Nucleotide Exchange Factors, Humans, RNA Interference, Extracellular Signal-Regulated MAP Kinases, rhoA GTP-Binding Protein, Cells, Cultured, Rho Guanine Nucleotide Exchange Factors
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influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
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