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四肢骨骼的形态发生与畸形发生

Morphogenesis and dysmorphogenesis of the appendicular skeleton.

作者信息

Shum Lillian, Coleman Cynthia M, Hatakeyama Yuji, Tuan Rocky S

机构信息

Cartilage Biology and Orthopaedics Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Building 50, Room 1503, MSC 8022, Bethesda, MD 20892, USA.

出版信息

Birth Defects Res C Embryo Today. 2003 May;69(2):102-22. doi: 10.1002/bdrc.10012.

Abstract

Cartilage patterning and differentiation are prerequisites for skeletal development through endochondral ossification (EO). Multipotential mesenchymal cells undergo a complex process of cell fate determination to become chondroprogenitors and eventually differentiate into chondrocytes. These developmental processes require the orchestration of cell-cell and cell-matrix interactions. In this review, we present limb bud development as a model for cartilage patterning and differentiation. We summarize the molecular and cellular events and signaling pathways for axis patterning, cell condensation, cell fate determination, digit formation, interdigital apoptosis, EO, and joint formation. The interconnected nature of these pathways underscores the effects of genetic and teratogenic perturbations that result in skeletal birth defects. The topics reviewed also include limb dysmorphogenesis as a result of genetic disorders and environmental factors, including FGFR, GLI3, GDF5/CDMP1, Sox9, and Cbfa1 mutations, as well as thalidomide- and alcohol-induced malformations. Understanding the complex interactions involved in cartilage development and EO provides insight into mechanisms underlying the biology of normal cartilage, congenital disorders, and pathologic adult cartilage.

摘要

软骨的模式形成和分化是通过软骨内成骨(EO)进行骨骼发育的先决条件。多能间充质细胞经历复杂的细胞命运决定过程,成为软骨祖细胞并最终分化为软骨细胞。这些发育过程需要细胞间和细胞与基质相互作用的协调。在本综述中,我们将肢芽发育作为软骨模式形成和分化的模型。我们总结了轴模式形成、细胞凝聚、细胞命运决定、指(趾)形成、指间细胞凋亡、EO和关节形成的分子和细胞事件以及信号通路。这些通路的相互联系性质强调了导致骨骼出生缺陷的遗传和致畸扰动的影响。所综述的主题还包括由遗传疾病和环境因素导致的肢体畸形发生,包括FGFR、GLI3、GDF5/CDMP1、Sox9和Cbfa1突变,以及沙利度胺和酒精诱导的畸形。了解软骨发育和EO中涉及的复杂相互作用,有助于深入了解正常软骨生物学、先天性疾病和病理性成人软骨的潜在机制。

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