Cell signaling in tenocytes: Response to load and ligands in health and disease

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Abstract

Signaling in tenocytes during development, homeostasis and injury involves multiple and redundant pathways. Given that tendons transmit mechanical forces from muscle to bone to effect movement, a key function for tenocytes is the detection of and response to mechanical stimulation. Mechanotransduction involves matrix-integrin-cytoskeleton to nucleus signaling, gap junction intercellular communication, changes in intracellular calcium (Ca2+), activation of receptors and their pathways, and responses to biochemical factors such as hormones, growth factors, adenosine triphosphate (ATP) and its derivatives, and neuromodulators. The primary cilium also plays a key role in the detection of mechanical signals. During development, transforming growth factor-β (TGF-β), bone morphogenetic protein (BMP), and hedgehog (Hh) signaling modulate tendon differentiation and formation. The response to injury is complex and varied involving not only inflammatory mediators such as interleukin-1β but also mechanosensing. This chapter reviews the signaling pathways tenocytes use during mechanotransduction, development and in response to injury.

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Wall, M. E., Dyment, N. A., Bodle, J., Volmer, J., Loboa, E., Cederlund, A., … Banes, A. J. (2016). Cell signaling in tenocytes: Response to load and ligands in health and disease. Advances in Experimental Medicine and Biology. Springer New York LLC. https://doi.org/10.1007/978-3-319-33943-6_7

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