Ligament Cell Biology: Effect of Mechanical Loading.

IF 2.5 Q3 CELL BIOLOGY
Mikołaj Stańczak, Maciej Biały, Magdalena Hagner-Derengowska
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引用次数: 0

Abstract

Ligaments are biomechanically specialized connective tissues that maintain joint stability and guide motion under complex loading conditions. At the cellular and molecular levels, ligament homeostasis is governed by fibroblast-like cells (ligamentocytes) embedded in an intricately organized ECM composed predominantly of type I collagen, with contributions from type III collagen, elastin, proteoglycans, and glycoproteins. These cells continuously sense and respond to mechanical stimuli-tension, compression, and shear-through mechanotransduction pathways involving integrins, focal adhesions, cytoskeletal remodeling, and mechanosensitive ion channels. Downstream signaling cascades, including MAPKs and PI3K/AKT, integrate biomechanical cues with growth factor and cytokine signaling to fine-tune gene expression, collagen fibrillogenesis, and ECM turnover. Distinct from tendons, ligaments must adapt to multidirectional loads, resulting in unique ECM compositions and cellular phenotypes. Appropriate mechanical loading maintains collagen alignment, promotes ECM integrity, and stabilizes the ligament cell phenotype. By contrast, insufficient or excessive load alters the molecular balance, triggering catabolic processes, inflammation, and disorganized ECM assembly. This delicate equilibrium also underlies the ligamentization observed in ACL graft remodeling, where controlled mechanical environments and molecular interventions accelerate the acquisition of ligamentous properties. Emerging insights into transcriptional and epigenetic regulation, growth factor-mediated cues, and cytokine-driven responses offer avenues to engineer ligament-like tissues and optimize recovery strategies. By leveraging molecular knowledge of cell-matrix interactions, growth factor profiles, and genetic/epigenetic modulators, clinicians and researchers can design tailored loading protocols, biomimetic scaffolds, and regenerative therapies. These approaches aim to restore ligament functionality, enhance graft integration, and prevent degenerative changes, ultimately improving patient outcomes in ligament injury repair and reconstruction.

韧带细胞生物学:机械负荷的影响。
韧带是生物力学上专门的结缔组织,在复杂的负载条件下维持关节稳定性和引导运动。在细胞和分子水平上,韧带的内稳态是由成纤维细胞样细胞(韧带细胞)控制的,这些细胞嵌入在由I型胶原组成的复杂组织的ECM中,其中包括III型胶原、弹性蛋白、蛋白聚糖和糖蛋白。这些细胞通过包括整合素、局灶黏附、细胞骨架重塑和机械敏感离子通道在内的机械转导途径,不断感知和响应机械刺激——张力、压缩和剪切。下游信号级联,包括MAPKs和PI3K/AKT,将生物力学信号与生长因子和细胞因子信号结合起来,微调基因表达、胶原纤维形成和ECM转换。与肌腱不同,韧带必须适应多向负荷,从而产生独特的ECM成分和细胞表型。适当的机械负荷维持胶原排列,促进ECM的完整性,并稳定韧带细胞表型。相反,负荷不足或负荷过大会改变分子平衡,引发分解代谢过程、炎症和ECM组装紊乱。这种微妙的平衡也是在ACL移植物重塑中观察到的韧带化的基础,在这种情况下,受控的机械环境和分子干预加速了韧带特性的获得。对转录和表观遗传调控、生长因子介导的线索和细胞因子驱动的反应的新见解为设计韧带样组织和优化恢复策略提供了途径。通过利用细胞-基质相互作用、生长因子谱和遗传/表观遗传调节剂的分子知识,临床医生和研究人员可以设计定制的加载方案、仿生支架和再生疗法。这些方法旨在恢复韧带功能,增强移植物整合,防止退行性改变,最终改善韧带损伤修复和重建的患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
86
审稿时长
1 months
期刊介绍: Cellular Physiology and Biochemistry is a multidisciplinary scientific forum dedicated to advancing the frontiers of basic cellular research. It addresses scientists from both the physiological and biochemical disciplines as well as related fields such as genetics, molecular biology, pathophysiology, pathobiochemistry and cellular toxicology & pharmacology. Original papers and reviews on the mechanisms of intracellular transmission, cellular metabolism, cell growth, differentiation and death, ion channels and carriers, and the maintenance, regulation and disturbances of cell volume are presented. Appearing monthly under peer review, Cellular Physiology and Biochemistry takes an active role in the concerted international effort to unravel the mechanisms of cellular function.
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