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Mechanical Control of Myotendinous Junction Formation and Tendon Differentiation During Development

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Specialty Cell Biology
Date 2017 Apr 8
PMID 28386542
Citations 19
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Abstract

The development of the musculoskeletal system is a great model to study the interplay between chemical and mechanical inter-tissue signaling in cell adhesion, tissue morphogenesis and differentiation. In both vertebrates and invertebrates (e.g., ) the formation of muscle-tendon interaction generates mechanical forces which are required for myotendinous junction maturation and tissue differentiation. In addition, these forces must be withstood by muscles and tendons in order to prevent detachment from each other, deformation or even losing their integrity. Extracellular matrix remodeling at the myotendinous junction is key to resist mechanical load generated by muscle contraction. Recent evidences in vertebrates indicate that mechanical forces generated during junction formation regulate chemical signaling leading to extracellular matrix remodeling, however, the mechanotransduction mechanisms associated to this response remains elusive. In addition to extracellular matrix remodeling, the ability of tendon-cells to bear mechanical load depends on rearrangement of tendon cell cytoskeleton, thus studying the molecular mechanisms involved in this process is critical to understand the contribution of mechanical forces to the development of the musculoskeletal system. Here, we review recent findings regarding the role of chemical and mechanical signaling in myotendinous junction formation and tendon differentiation, and discuss molecular mechanisms of mechanotransduction that may allow tendon cells to withstand mechanical load during development of the musculoskeletal system.

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References
1.
Farge E . Mechanical induction of Twist in the Drosophila foregut/stomodeal primordium. Curr Biol. 2003; 13(16):1365-77. DOI: 10.1016/s0960-9822(03)00576-1. View

2.
Gilsohn E, Volk T . Slowdown promotes muscle integrity by modulating integrin-mediated adhesion at the myotendinous junction. Development. 2010; 137(5):785-94. DOI: 10.1242/dev.043703. View

3.
North T, Goessling W, Peeters M, Li P, Ceol C, Lord A . Hematopoietic stem cell development is dependent on blood flow. Cell. 2009; 137(4):736-48. PMC: 2722870. DOI: 10.1016/j.cell.2009.04.023. View

4.
Chanana B, Graf R, Koledachkina T, Pflanz R, Vorbruggen G . AlphaPS2 integrin-mediated muscle attachment in Drosophila requires the ECM protein Thrombospondin. Mech Dev. 2007; 124(6):463-75. DOI: 10.1016/j.mod.2007.03.005. View

5.
Takagi J, Strokovich K, Springer T, Walz T . Structure of integrin alpha5beta1 in complex with fibronectin. EMBO J. 2003; 22(18):4607-15. PMC: 212714. DOI: 10.1093/emboj/cdg445. View