Mechanical forces play an important role in regulating tissue development and homeostasis in multiple cell types including bone, joint, epithelial and vascular cells, and are also implicated in the development of diseases, e.g. osteoporosis, cardiovascular disease and osteoarthritis. Defining the mechanisms by which cells sense and respond to mechanical forces therefore has important implications for our understanding of tissue function in health and disease and may lead to the identification of targets for therapeutic intervention. Mechanoactivation of the Wnt signalling pathway was first identified in osteoblasts with a key role for β-catenin demonstrated in loading-induced osteogenesis. Since then, mechanoregulation of the Wnt pathway has also been observed in stem cells, epithelium, chondrocytes and vascular and lymphatic endothelium. Wnt can signal through both canonical and non-canonical pathways, and evidence suggests that both can mediate responses to mechanical strain, stretch and shear stress. This review will discuss our current understanding of the activation of the Wnt pathway in response to mechanical forces.
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Cover Image
Cover Image
The image represents talin in focal adhesions. Talin is a mechanosensitive molecule that connects the integrin receptors in the cell membrane with the cytoskeleton. It is exposed to mechanical stretching, which induces the unfolding of its structure. This controls talin's interaction with other proteins, such as Deleted in Liver Cancer (DLC), which is a tumour suppressor and negative regulator of cell contractility. To learn more about this, please see the articles in this issue by Burridge (pages 673–675), Barnett and Kanchanawong (pages 677–680), and Popa and Berkovich (pages 687–699). The image was prepared by Magdalena von Essen, background picture: Vesa Hytönen.
Mechanoactivation of Wnt/β-catenin pathways in health and disease Available to Purchase
Armando del Río Hernández, Christina M. Warboys; Mechanoactivation of Wnt/β-catenin pathways in health and disease. Emerg Top Life Sci 21 December 2018; 2 (5): 701–712. doi: https://doi.org/10.1042/ETLS20180042
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