Tam Kenneth T, Baar Keith
Biomedical Engineering Graduate Group, University of California Davis, Davis, CA 95616, USA; Department of Neurobiology, Physiology and Behavior, University of California Davis, Davis, CA 95616, USA.
Biomedical Engineering Graduate Group, University of California Davis, Davis, CA 95616, USA; Department of Neurobiology, Physiology and Behavior, University of California Davis, Davis, CA 95616, USA; Department of Physiology and Membrane Biology, University of California Davis, Davis, CA 95616, USA; VA Northern California Health Care System, Mather, CA 95655, USA.
Matrix Biol. 2025 Feb;135:39-54. doi: 10.1016/j.matbio.2024.12.001. Epub 2024 Dec 5.
Tendon and ligament injuries are highly prevalent but heal poorly, even with proper care. Restoration of native tissue function is complicated by the fact that these tissues vary anatomically in terms of their mechanical properties, composition, and structure. These differences develop as adaptations to diverse mechanical demands; however, pathology may alter the loads placed on the tissue. Musculoskeletal loads can be generally categorized into tension, compression, and shear. Each of these regulate distinct molecular pathways that are involved in tissue remodeling, including many of the canonical tenogenic genes. In this review, we provide a perspective on the stage-specific regulation of mechanically sensitive pathways during development and maturation of tendon and ligament tissue, including scleraxis, mohawk, and others. Furthermore, we discuss structural features of healing and diseased tendon that may contribute to aberrant loading profiles, and how the associated disturbance in molecular signaling may contribute to incomplete healing or the formation of degenerative phenotypes. The perspectives provided here draw from studies spanning in vitro, animal, and human experiments of healthy and diseased tendon to propose a more targeted approach to advance rehabilitation, orthobiologics, and tissue engineering.
肌腱和韧带损伤非常普遍,即使得到妥善护理,愈合情况也很差。由于这些组织在力学性能、组成和结构方面存在解剖学差异,恢复其天然组织功能变得很复杂。这些差异是作为对不同力学需求的适应而产生的;然而,病理情况可能会改变施加在组织上的负荷。肌肉骨骼负荷通常可分为张力、压缩力和剪切力。这些负荷各自调节参与组织重塑的不同分子途径,包括许多典型的肌腱生成基因。在本综述中,我们阐述了在肌腱和韧带组织发育和成熟过程中机械敏感途径的阶段特异性调节,包括硬骨素、莫霍克基因等。此外,我们讨论了愈合和患病肌腱的结构特征,这些特征可能导致异常的负荷分布,以及分子信号传导中的相关紊乱如何可能导致愈合不完全或退行性表型的形成。这里提供的观点来自对健康和患病肌腱的体外、动物和人体实验的研究,旨在提出一种更具针对性的方法,以推进康复、 orthobiologics(这个词不太常见,可能有误,暂保留英文)和组织工程。