Regulatory mechanisms for the development of growth plate cartilage

被引:68
作者
Michigami, Toshimi [1 ,2 ]
机构
[1] Osaka Med Ctr, Dept Bone & Mineral Res, Izumi, Osaka 5941101, Japan
[2] Res Inst Maternal & Child Hlth, Izumi, Osaka 5941101, Japan
关键词
Chondrocyte; Transcription factors; Growth factors; Extracellular matrix; Differentiation; MATRIX-METALLOPROTEINASE; 13; HYPERTROPHIC CHONDROCYTE DIFFERENTIATION; AUTOSOMAL SEX REVERSAL; FACTOR RECEPTOR-3; NATRIURETIC PEPTIDE; ENDOCHONDRAL OSSIFICATION; MICE LACKING; CAMPOMELIC DYSPLASIA; DEVELOPMENT SUGGESTS; INTEGRIN EXPRESSION;
D O I
10.1007/s00018-013-1346-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:4213 / 4221
页数:9
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