Deanery of Biomedical Sciences, University of Edinburgh, Hugh Robson Building, George Square, Edinburgh, Scotland, EH8 9XD, UK.
Curr Rheumatol Rep. 2019 Jun 15;21(8):38. doi: 10.1007/s11926-019-0837-6.
Articular chondrocytes are exclusively responsible for the turnover of the extracellular matrix (ECM) of hyaline cartilage. However, chondrocytes are phenotypically unstable and, if they de-differentiate into hypertrophic or fibroblastic forms, will produce a defective and weak matrix. Chondrocyte volume and morphology exert a strong influence over phenotype and a full appreciation of the factors controlling chondrocyte phenotype stability is central to understanding (a) the mechanisms underlying the cartilage failure in osteoarthritis (OA), (b) the rationale for hyaline cartilage repair, and (c) the strategies for improving the engineering of resilient cartilage. The focus of this review is on the factors involved in, and the importance of regulating, chondrocyte morphology and volume as key controllers of chondrocyte phenotype.
The visualisation of fluorescently-labelled in situ chondrocytes within non-degenerate and mildly degenerate cartilage, by confocal scanning laser microscopy (CLSM) and imaging software, has identified the marked heterogeneity of chondrocyte volume and morphology. The presence of chondrocytes with cytoplasmic processes, increased volume, and clustering suggests important early changes to their phenotype. Results from experiments more closely aligned to the normal physico-chemical environment of in situ chondrocytes are emphasising the importance of understanding the factors controlling chondrocyte morphology and volume that ultimately affect phenotype. An appreciation of the importance of chondrocyte volume and morphology for controlling the chondrocyte phenotype is advancing at a rapid pace and holds particular promise for developing strategies for protecting the chondrocytes against deleterious changes and thereby maintaining healthy and resilient cartilage.
关节软骨细胞是透明软骨细胞外基质(ECM)更新的唯一来源。然而,软骨细胞表型不稳定,如果它们去分化为肥大或成纤维样形式,将产生有缺陷和脆弱的基质。软骨细胞的体积和形态对表型有很强的影响,充分了解控制软骨细胞表型稳定性的因素对于理解(a)骨关节炎(OA)软骨衰竭的机制、(b)透明软骨修复的原理以及(c)提高弹性软骨工程的策略至关重要。本综述的重点是参与和调节软骨细胞形态和体积的因素,以及软骨细胞形态和体积作为软骨细胞表型关键控制器的重要性。
通过共聚焦扫描激光显微镜(CLSM)和成像软件对非退变和轻度退变软骨中荧光标记原位软骨细胞的可视化,已经确定了软骨细胞体积和形态的明显异质性。存在具有细胞质突起、体积增加和聚集的软骨细胞表明其表型发生了重要的早期变化。更接近原位软骨细胞正常物理化学环境的实验结果强调了理解控制软骨细胞形态和体积的因素的重要性,这些因素最终影响表型。对软骨细胞体积和形态控制软骨细胞表型的重要性的认识正在迅速发展,并为开发保护软骨细胞免受有害变化的策略从而维持健康和有弹性的软骨提供了特别的希望。