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肌腱愈合会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。

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

机构信息

McKay Orthopedic Research Laboratory, University of Pennsylvania, 110 Stemmler Hall, 3450 Hamilton Walk, Philadelphia, PA 19104-6081, USA.

Department of Biomedical Engineering, Drexel University, Philadelphia, PA, USA.

出版信息

J R Soc Interface. 2018 Feb;15(139). doi: 10.1098/rsif.2017.0880.

Abstract

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.

摘要

在束、纤维和原纤维水平的机械加载下,肌腱的细胞外基质经历多种多尺度变化。例如,肌腱的拉伸加载会增加其刚度,组织胶原纤维,并增加加载方向上的细胞应变。尽管施加的宏观应变与未受伤肌腱中的细胞和核应变相关,但肌腱愈合过程中的多尺度反应仍然未知,可能会影响细胞的机械感受和反应。因此,本研究评估了未受伤和愈合肌腱对准静态拉伸加载的多尺度结构-功能机制。我们发现,肌腱愈合会影响机械加载的宏观力学和结构响应,这表现在应变硬化和胶原纤维重新排列的减少。在微观和纳米尺度上,与未受伤的肌腱相比,愈合导致胶原纤维的无序化增加、核的无序化增加、核纵横比随加载的变化减少以及压痕模量降低。总之,这项工作支持了在肌腱愈合过程中核应变传递衰减的新概念,并确定了可能起作用的几个多尺度特性。我们的工作还为肌腱细胞在细胞输送治疗后可能经历的生物力学微环境提供了基准。

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