Nishimura Riko, Hata Kenji, Nakamura Eriko, Murakami Tomohiko, Takahata Yoshifumi
Department of Molecular and Cellular Biochemistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Histochem Cell Biol. 2018 Apr;149(4):353-363. doi: 10.1007/s00418-017-1628-7. Epub 2018 Jan 8.
Transcription factors play important roles in the regulation of cartilage development by controlling the expression of chondrogenic genes. Genetic studies have revealed that Sox9/Sox5/Sox6, Runx2/Runx3 and Osterix in particular are essential for the sequential steps of cartilage development. Importantly, these transcription factors form network systems that are also required for appropriate cartilage development. Molecular cloning approaches have largely contributed to the identification of several transcriptional partners for Sox9 and Runx2 during cartilage development. Although the importance of a negative-feedback loop between Indian hedgehog (Ihh) and parathyroid hormone-related protein (PTHrP) in chondrocyte hypertrophy has been well established, recent studies indicate that several transcription factors interact with the Ihh-PTHrP loop and demonstrated that Ihh has multiple functions in the regulation of cartilage development. The most common cartilage disorder, osteoarthritis, has been reported to result from the pathological action of several transcription factors, including Runx2, C/EBPβ and HIF-2α. On the other hand, NFAT family members appear to play roles in the protection of cartilage from osteoarthritis. It is also becoming important to understand the homeostasis and regulation of articular chondrocytes, because they have different cellular and molecular features from chondrocytes of the growth plate. This review summarizes the regulation and roles of transcriptional network systems in cartilage development and their pathological roles in osteoarthritis.
转录因子通过控制软骨生成基因的表达,在软骨发育的调控中发挥重要作用。遗传学研究表明,Sox9/Sox5/Sox6、Runx2/Runx3和Osterix尤其对软骨发育的连续步骤至关重要。重要的是,这些转录因子形成了对适当软骨发育也必不可少的网络系统。分子克隆方法在很大程度上有助于鉴定软骨发育过程中Sox9和Runx2的几个转录伙伴。尽管印度刺猬因子(Ihh)和甲状旁腺激素相关蛋白(PTHrP)之间的负反馈环在软骨细胞肥大中的重要性已得到充分证实,但最近的研究表明,几种转录因子与Ihh-PTHrP环相互作用,并证明Ihh在软骨发育调控中具有多种功能。据报道,最常见的软骨疾病骨关节炎是由包括Runx2、C/EBPβ和HIF-2α在内的几种转录因子的病理作用引起的。另一方面,NFAT家族成员似乎在保护软骨免受骨关节炎影响方面发挥作用。了解关节软骨细胞的稳态和调控也变得很重要,因为它们具有与生长板软骨细胞不同的细胞和分子特征。本综述总结了转录网络系统在软骨发育中的调控和作用及其在骨关节炎中的病理作用。