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Tendon healing affects the multiscale mechanical structural and compositional response of tendon to quasi-static tensile loading

机译:肌腱愈合影响肌腱对准静态拉伸载荷的多尺度力学结构和组成响应

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摘要

Tendon experiences a variety of multiscale changes to its extracellular matrix during mechanical loading at the fascicle, fibre and fibril levels. For example, tensile loading of tendon increases its stiffness, with organization of collagen fibres, and increases cell strain in the direction of loading. Although applied macroscale strains correlate to cell and nuclear strains in uninjured tendon, the multiscale response during tendon healing remains unknown and may affect cell mechanosensing and response. Therefore, this study evaluated multiscale structure–function mechanisms in response to quasi-static tensile loading in uninjured and healing tendons. We found that tendon healing affected the macroscale mechanical and structural response to mechanical loading, evidenced by decreases in strain stiffening and collagen fibre realignment. At the micro- and nanoscales, healing resulted in increased collagen fibre disorganization, nuclear disorganization, decreased change in nuclear aspect ratio with loading, and decreased indentation modulus compared to uninjured tendons. Taken together, this work supports a new concept of nuclear strain transfer attenuation during tendon healing and identifies several multiscale properties that may contribute. Our work also provides benchmarks for the biomechanical microenvironments that tendon cells may experience following cell delivery therapies.
机译:肌腱在纤维束,纤维和原纤维水平的机械加载过程中会经历多种细胞外基质的多尺度变化。例如,肌腱的拉伸载荷随着胶原纤维的组织而增加了其刚度,并且在载荷方向上增加了细胞应变。尽管所施加的宏观应变与未损伤的肌腱中的细胞和核应变相关,但是在肌腱愈合期间的多尺度响应仍然未知,并且可能影响细胞的机械传感和响应。因此,本研究评估了对未受伤和愈合的肌腱准静态拉伸载荷的响应的多尺度结构-功能机制。我们发现,肌腱愈合影响了对机械负荷的宏观力学和结构响应,这由应变变硬和胶原纤维重新排列的减少证明。与未受伤的肌腱相比,在微米和纳米尺度上,愈合导致胶原纤维分解度增加,核分解度降低,核长径比随载荷的变化减小,压痕模量降低。综上所述,这项工作支持了腱修复过程中核应变传递衰减的新概念,并确定了可能有贡献的多个多尺度特性。我们的工作还为腱细胞在细胞递送疗法后可能经历的生物力学微环境提供了基准。

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