Department of Orthopedic Surgery, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Department of Orthopedic Surgery, Qingdao Municipal Hospital, University of Health and Rehabilitation Sciences, Qingdao, China.
Front Endocrinol (Lausanne). 2024 Nov 6;15:1485876. doi: 10.3389/fendo.2024.1485876. eCollection 2024.
Tendons are fibrous connective tissues that transmit force from muscles to bones. Despite their ability to withstand various loads, tendons are susceptible to significant damage. The healing process of tendons and ligaments connected to bone surfaces after injury presents a clinical challenge due to the intricate structure, composition, cellular populations, and mechanics of the interface. Inflammation plays a pivotal role in tendon healing, creating an inflammatory microenvironment through cytokines and immune cells that aid in debris clearance, tendon cell proliferation, and collagen fiber formation. However, uncontrolled inflammation can lead to tissue damage, and adhesions, and impede proper tendon healing, culminating in scar tissue formation. Therefore, precise regulation of inflammation is crucial. This review offers insights into the impact of inflammation on tendon-bone healing and its underlying mechanisms. Understanding the inflammatory microenvironment, cellular interactions, and extracellular matrix dynamics is essential for promoting optimal healing of tendon-bone injuries. The roles of fibroblasts, inflammatory cytokines, chemokines, and growth factors in promoting healing, inhibiting scar formation, and facilitating tissue regeneration are discussed, highlighting the necessity of balancing the suppression of detrimental inflammatory responses with the promotion of beneficial aspects to enhance tendon healing outcomes. Additionally, the review explores the significant implications and translational potential of targeted inflammatory modulation therapies in refining strategies for tendon-bone healing treatments.
肌腱是一种纤维结缔组织,将力量从肌肉传递到骨骼。尽管它们能够承受各种负荷,但肌腱很容易受到严重的损伤。受伤后与骨表面相连的肌腱和韧带的愈合过程是一个临床挑战,因为其结构、组成、细胞群体和界面力学都很复杂。炎症在肌腱愈合中起着关键作用,通过细胞因子和免疫细胞产生炎症微环境,有助于清除碎片、肌腱细胞增殖和胶原纤维形成。然而,失控的炎症会导致组织损伤和粘连,并阻碍适当的肌腱愈合,最终形成疤痕组织。因此,精确调节炎症至关重要。本综述探讨了炎症对肌腱-骨愈合的影响及其潜在机制。了解炎症微环境、细胞相互作用和细胞外基质动力学对于促进肌腱-骨损伤的最佳愈合至关重要。讨论了成纤维细胞、炎症细胞因子、趋化因子和生长因子在促进愈合、抑制疤痕形成和促进组织再生方面的作用,强调了抑制有害炎症反应和促进有益方面的必要性,以提高肌腱愈合效果。此外,该综述探讨了靶向炎症调节治疗在改进肌腱-骨愈合治疗策略方面的重要意义和转化潜力。