Purpose: We hypothesized that the relationship between mechanical stress during development and embryonic and neonatal tendon formation in the mouse model might be applied to prevent disease and treat tendon regeneration in humans. In this study, we focused on movement, particularly exercise. This study aimed to explore changes in mechanical stress and reactions of muscle-tendon complexes.
Methods: We used Wild-type C57BL/6 mice. Motor Tests: the neurobehavioral development of the mouse pups was tested to evaluate their general motor function, including surface righting and ambulation. qPCR: The muscle and tendon responses were examined to determine the expression of genes associated with growth factor at nine-time points. Histology: For histological evaluation, the limbs were sectioned focus on the Achilles Tendon at 12 μm thickness, and stained with Alcian blue, Hematoxylin and eosin, and Picrosirius red to visualize collagen.
Results: We showed that movement is critical for the development of molecular mechanisms at different stages of growth. We captured four phases of changes in the mechanical force of the limbs. We suggest that tendon response to mechanical stimulation is fundamentally altered by biochemical signals. Collectively, these results show that the neonatal tendon development process goes through a continuous change in mechanical force followed by the expression of growth factor markers.
Conclusion: The results of this study demonstrated the importance of mechanical stress in TGF-β and Scx expression for tendon development. These findings may provide a therapeutic target for a disorder in children and tendon-related diseases.
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