Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hajdu-Bihar, Hungary.
MSK Lab, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, UK.
Cartilage. 2021 Dec;13(2_suppl):53S-67S. doi: 10.1177/1947603520903425. Epub 2020 Feb 14.
Circadian rhythms in cartilage homeostasis are hypothesized to temporally segregate and synchronize the activities of chondrocytes to different times of the day, and thus may provide an efficient mechanism by which articular cartilage can recover following physical activity. While the circadian clock is clearly involved in chondrocyte homeostasis in health and disease, it is unclear as to what roles it may play during early chondrogenesis.
The purpose of this study was to determine whether the rhythmic expression of the core circadian clock was detectable at the earliest stages of chondrocyte differentiation, and if so, whether a synchronized expression pattern of chondrogenic transcription factors and developing cartilage matrix constituents was present during cartilage formation.
Following serum shock, embryonic limb bud-derived chondrifying micromass cultures exhibited synchronized temporal expression patterns of core clock genes involved in the molecular circadian clock. We also observed that chondrogenic marker genes followed a circadian oscillatory pattern. Clock synchronization significantly enhanced cartilage matrix production and elevated , and gene expression. The observed chondrogenesis-promoting effect of the serum shock was likely attributable to its synchronizing effect on the molecular clockwork, as co-application of small molecule modulators (longdaysin and KL001) abolished the stimulating effects on extracellular matrix production and chondrogenic marker gene expression.
Results from this study suggest that a functional molecular clockwork plays a positive role in tissue homeostasis and histogenesis during early chondrogenesis.
昼夜节律被假设在软骨稳态中具有时间分离和同步软骨细胞活动的作用,使其能够在一天中的不同时间恢复关节软骨的活力。虽然昼夜节律时钟显然在健康和疾病中的软骨细胞稳态中起作用,但尚不清楚它在早期软骨发生过程中可能发挥什么作用。
本研究旨在确定核心昼夜节律时钟的节律表达是否在软骨细胞分化的最早阶段可检测到,如果是这样,在软骨形成过程中是否存在软骨形成转录因子和发育中的软骨基质成分的同步表达模式。
血清休克后,胚胎肢芽来源的软骨化微团培养物表现出参与分子昼夜节律的核心时钟基因的同步时间表达模式。我们还观察到,软骨形成标志物基因呈昼夜振荡模式。时钟同步显著增强了软骨基质的产生,并提高了 和 基因的表达。血清休克的观察到的促软骨生成作用可能归因于其对分子时钟的同步作用,因为小分子调节剂(longdaysin 和 KL001)的共同应用消除了对细胞外基质产生和软骨形成标志物基因表达的刺激作用。
本研究结果表明,功能分子时钟在早期软骨发生过程中的组织稳态和组织发生中发挥积极作用。