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软骨发育与疾病中的转录网络系统

Transcriptional network systems in cartilage development and disease.

作者信息

Nishimura Riko, Hata Kenji, Nakamura Eriko, Murakami Tomohiko, Takahata Yoshifumi

机构信息

Department of Molecular and Cellular Biochemistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

出版信息

Histochem Cell Biol. 2018 Apr;149(4):353-363. doi: 10.1007/s00418-017-1628-7. Epub 2018 Jan 8.

DOI:10.1007/s00418-017-1628-7
PMID:29308531
Abstract

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.

摘要

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。

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Transcriptional network systems in cartilage development and disease.软骨发育与疾病中的转录网络系统
Histochem Cell Biol. 2018 Apr;149(4):353-363. doi: 10.1007/s00418-017-1628-7. Epub 2018 Jan 8.
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The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6.转录因子Sox9在软骨细胞分化途径的连续步骤中发挥着重要作用,并且是Sox5和Sox6表达所必需的。
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C/EBPβ and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2α as the inducer in chondrocytes.C/EBPβ 和 RUNX2 通过 MMP-13 作为靶点和 HIF-2α 作为诱导物在软骨细胞中合作降解软骨。
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ALK2 functions as a BMP type I receptor and induces Indian hedgehog in chondrocytes during skeletal development.ALK2作为一种骨形态发生蛋白(BMP)I型受体,在骨骼发育过程中诱导软骨细胞产生印度刺猬蛋白。
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Sox5 and Sox6 are needed to develop and maintain source, columnar, and hypertrophic chondrocytes in the cartilage growth plate.Sox5和Sox6是软骨生长板中发育和维持源细胞、柱状细胞和肥大软骨细胞所必需的。
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Parathyroid hormone-related protein is induced by hypoxia and promotes expression of the differentiated phenotype of human articular chondrocytes.甲状旁腺激素相关蛋白由缺氧诱导,并促进人关节软骨细胞分化表型的表达。
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PTHrP and skeletal development.甲状旁腺激素相关蛋白与骨骼发育
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Regulation of Cartilage Development and Diseases by Transcription Factors.转录因子对软骨发育和疾病的调控
J Bone Metab. 2017 Aug;24(3):147-153. doi: 10.11005/jbm.2017.24.3.147. Epub 2017 Aug 31.
2
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N Engl J Med. 2017 Feb 16;376(7):652-662. doi: 10.1056/NEJMoa1608345.
3
Achondroplasia: Development, pathogenesis, and therapy.软骨发育不全:发育、发病机制及治疗
Int J Mol Sci. 2023 Nov 11;24(22):16209. doi: 10.3390/ijms242216209.
4
Roles of Skeletal Muscle in Development: A Bioinformatics and Systems Biology Overview.骨骼肌在发育中的作用:生物信息学与系统生物学概述
Adv Anat Embryol Cell Biol. 2023;236:21-55. doi: 10.1007/978-3-031-38215-4_2.
5
Single‑cell sequencing, genetics, and epigenetics reveal mesenchymal stem cell senescence in osteoarthritis (Review).单细胞测序、遗传学和表观遗传学揭示骨关节炎中间充质干细胞衰老(综述)。
Int J Mol Med. 2024 Jan;53(1). doi: 10.3892/ijmm.2023.5326. Epub 2023 Nov 8.
6
The role of E3 ubiquitin ligases in bone homeostasis and related diseases.E3泛素连接酶在骨稳态及相关疾病中的作用。
Acta Pharm Sin B. 2023 Oct;13(10):3963-3987. doi: 10.1016/j.apsb.2023.06.016. Epub 2023 Jul 6.
7
Multiple roles of ALK3 in osteoarthritis.ALK3在骨关节炎中的多种作用。
Bone Joint Res. 2023 Jul 3;12(7):397-411. doi: 10.1302/2046-3758.127.BJR-2022-0310.R1.
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Augmentation of BMP Signaling in Cranial Neural Crest Cells Leads to Premature Cranial Sutures Fusion through Endochondral Ossification in Mice.颅骨神经嵴细胞中骨形态发生蛋白信号增强通过软骨内成骨导致小鼠颅骨缝过早融合。
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