Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.
Cells. 2024 Mar 14;13(6):512. doi: 10.3390/cells13060512.
Hypoxia-inducible factor-1 (HIF-1) is a heterodimer transcription factor composed of an alpha and a beta subunit. HIF-1α is a master regulator of cellular response to hypoxia by activating the transcription of genes that facilitate metabolic adaptation to hypoxia. Since chondrocytes in mature articular cartilage reside in a hypoxic environment, HIF-1α plays an important role in chondrogenesis and in the physiological lifecycle of articular cartilage. Accumulating evidence suggests interactions between the HIF pathways and the circadian clock. The circadian clock is an emerging regulator in both developing and mature chondrocytes. However, how circadian rhythm is established during the early steps of cartilage formation and through what signaling pathways it promotes the healthy chondrocyte phenotype is still not entirely known. This narrative review aims to deliver a concise analysis of the existing understanding of the dynamic interplay between HIF-1α and the molecular clock in chondrocytes, in states of both health and disease, while also incorporating creative interpretations. We explore diverse hypotheses regarding the intricate interactions among these pathways and propose relevant therapeutic strategies for cartilage disorders such as osteoarthritis.
缺氧诱导因子-1(HIF-1)是由一个α亚基和一个β亚基组成的异二聚体转录因子。HIF-1α通过激活促进细胞对缺氧适应的基因的转录,是细胞对缺氧反应的主要调节因子。由于成熟关节软骨中的软骨细胞处于缺氧环境中,HIF-1α在软骨发生和关节软骨的生理生命周期中发挥重要作用。越来越多的证据表明 HIF 途径与生物钟之间存在相互作用。生物钟是发育中和成熟软骨细胞中的新兴调节因子。然而,在软骨形成的早期阶段,生物钟是如何建立的,以及它通过什么信号通路促进健康的软骨细胞表型,目前还不完全清楚。这篇叙述性综述旨在对 HIF-1α 和软骨细胞中分子钟在健康和疾病状态下的动态相互作用的现有理解进行简要分析,同时也纳入了创造性的解释。我们探讨了这些途径之间复杂相互作用的各种假设,并提出了针对骨关节炎等软骨疾病的相关治疗策略。