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本文引用的文献

1
Regulated transcription of human matrix metalloproteinase 13 (MMP13) and interleukin-1β (IL1B) genes in chondrocytes depends on methylation of specific proximal promoter CpG sites.人类基质金属蛋白酶 13(MMP13)和白细胞介素 1β(IL1B)基因在软骨细胞中的调控转录依赖于特定近端启动子 CpG 位点的甲基化。
J Biol Chem. 2013 Apr 5;288(14):10061-10072. doi: 10.1074/jbc.M112.421156. Epub 2013 Feb 15.
2
Epigenetic regulation during fetal femur development: DNA methylation matters.胎儿股骨发育过程中的表观遗传调控:DNA 甲基化很重要。
PLoS One. 2013;8(1):e54957. doi: 10.1371/journal.pone.0054957. Epub 2013 Jan 28.
3
Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia.评价 CNP 类似物在模拟成骨不全症的 Fgfr3 小鼠模型中的治疗潜力。
Am J Hum Genet. 2012 Dec 7;91(6):1108-14. doi: 10.1016/j.ajhg.2012.10.014. Epub 2012 Nov 29.
4
HIF1α is a central regulator of collagen hydroxylation and secretion under hypoxia during bone development.HIF1α 是骨发育过程中缺氧条件下胶原羟化和分泌的核心调节因子。
Development. 2012 Dec 1;139(23):4473-83. doi: 10.1242/dev.083881. Epub 2012 Oct 24.
5
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene.一种与 cGMP 过度产生相关的过度生长疾病,其原因是利钠肽受体 2 基因的功能获得性突变。
PLoS One. 2012;7(8):e42180. doi: 10.1371/journal.pone.0042180. Epub 2012 Aug 3.
6
Osterix regulates calcification and degradation of chondrogenic matrices through matrix metalloproteinase 13 (MMP13) expression in association with transcription factor Runx2 during endochondral ossification.成骨细胞特异性转录因子 2(Runx2)通过基质金属蛋白酶 13(MMP13)的表达,在软骨内骨化过程中调节软骨细胞基质的钙化和降解。
J Biol Chem. 2012 Sep 28;287(40):33179-90. doi: 10.1074/jbc.M111.337063. Epub 2012 Aug 6.
7
FoxA family members are crucial regulators of the hypertrophic chondrocyte differentiation program.FoxA 家族成员是肥大软骨细胞分化程序的关键调节因子。
Dev Cell. 2012 May 15;22(5):927-39. doi: 10.1016/j.devcel.2012.03.011.
8
Matrix disruptions, growth, and degradation of cartilage with impaired sulfation.基质破坏,生长和降解软骨,硫酸化受损。
J Biol Chem. 2012 Jun 22;287(26):22030-42. doi: 10.1074/jbc.M110.116467. Epub 2012 May 3.
9
cAMP response element-binding (CREB) recruitment following a specific CpG demethylation leads to the elevated expression of the matrix metalloproteinase 13 in human articular chondrocytes and osteoarthritis.特定 CpG 去甲基化后 cAMP 反应元件结合(CREB)募集导致人关节软骨细胞和骨关节炎中基质金属蛋白酶 13 的表达升高。
FASEB J. 2012 Jul;26(7):3000-11. doi: 10.1096/fj.12-206367. Epub 2012 Apr 13.
10
Sox9 directs hypertrophic maturation and blocks osteoblast differentiation of growth plate chondrocytes.Sox9 指导生长板软骨细胞的肥大成熟,并阻止成骨细胞分化。
Dev Cell. 2012 Mar 13;22(3):597-609. doi: 10.1016/j.devcel.2011.12.024.

生长板软骨发育的调控机制。

Regulatory mechanisms for the development of growth plate cartilage.

机构信息

Department of Bone and Mineral Research, Osaka Medical Center and Research Institute for Maternal and Child Health, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan,

出版信息

Cell Mol Life Sci. 2013 Nov;70(22):4213-21. doi: 10.1007/s00018-013-1346-9. Epub 2013 May 4.

DOI:10.1007/s00018-013-1346-9
PMID:23640571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11113666/
Abstract

In vertebrates, most of the skeleton is formed through endochondral ossification. Endochondral bone formation is a complex process involving the mesenchymal condensation of undifferentiated cells, the proliferation of chondrocytes and their differentiation into hypertrophic chondrocytes, and mineralization. This process is tightly regulated by various factors including transcription factors, soluble mediators, extracellular matrices, and cell-cell and cell-matrix interactions. Defects of these factors often lead to skeletal dysplasias and short stature. Moreover, there is growing evidence that epigenetic and microRNA-mediated mechanisms also play critical roles in chondrogenesis. This review provides an overview of our current understanding of the regulators for the development of growth plate cartilage and their molecular mechanisms of action. A knowledge of the regulatory mechanisms underlying the proliferation and differentiation of chondrocytes will provide insights into future therapeutic options for skeletal disorders.

摘要

在脊椎动物中,大部分骨骼是通过软骨内骨化形成的。软骨内骨的形成是一个复杂的过程,涉及未分化细胞的间充质凝聚、软骨细胞的增殖及其分化为肥大软骨细胞,以及矿化。这个过程受到转录因子、可溶性介质、细胞外基质以及细胞-细胞和细胞-基质相互作用等多种因素的严格调控。这些因素的缺陷通常会导致骨骼发育不良和身材矮小。此外,越来越多的证据表明,表观遗传和 microRNA 介导的机制也在软骨生成中发挥关键作用。本综述概述了我们目前对生长板软骨发育的调控因子及其作用的分子机制的理解。了解软骨细胞增殖和分化的调控机制将为骨骼疾病的未来治疗选择提供思路。