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滑膜关节的发育

Development of synovial joints.

作者信息

Archer Charles W, Dowthwaite Gary P, Francis-West Philippa

机构信息

School of Biosciences, Cardiff Institute of Tissue Engineering and Repair, Cardiff University, Museum Avenue, Cardiff, CF1 3US, UK.

出版信息

Birth Defects Res C Embryo Today. 2003 May;69(2):144-55. doi: 10.1002/bdrc.10015.

Abstract

Synovial joints arise through two main processes. In long bone elements, cartilaginous differentiation occurs across the locations of the prospective joints that then segment secondarily. This process occurs through the development of a noncartilaginous region known as the interzone. The interzone becomes an important signaling center to the opposing elements, which can regulate growth through such factors as GDF-5. The interzone also expresses bone morphogenetic proteins (BMPs) and their antagonists, such as noggin. Overexpression of BMPs, or the loss of noggin leads to joint fusions. The interzone also expresses Wnt-14, which appears to be specific for this region in the developing anlagen, and regulates its nonchondrogenic nature. Cavitation of the joint follows, driven by selective high-level synthesis of hyaluronan by interzone cells and presumptive synovial cells. In addition, as the interzone disperses during cavity enlargement, data are now accruing that suggest that both the synovium and articular cartilage develop from this population. Finally, the development of articular cartilage progresses through appositional growth driven by a progenitor/stem cell subpopulation that resides in the articular surface. The individual elements of the skeleton are connected together at regions termed joints or articulations. Classically, there are three broad categories of joints: immovable joints (syntharthroses); mixed articulations, in which the range of movement is limited (amphiarthroses); and the movable, or synovial, joints (diarthroses). This review concentrates on the development of the synovial joints.

摘要

滑膜关节通过两个主要过程形成。在长骨元件中,软骨分化发生在未来关节的位置,然后这些位置会进行二次分割。这个过程通过一个称为中间带的非软骨区域的发育而发生。中间带成为对相对元件的重要信号中心,它可以通过诸如生长分化因子5(GDF-5)等因子调节生长。中间带还表达骨形态发生蛋白(BMPs)及其拮抗剂,如头蛋白。BMPs的过度表达或头蛋白的缺失会导致关节融合。中间带还表达Wnt-14,它似乎在发育中的原基中对该区域具有特异性,并调节其非软骨生成的性质。随后,在中间带细胞和假定的滑膜细胞选择性高水平合成透明质酸的驱动下,关节发生空化。此外,随着中间带在腔扩大过程中分散,现在有越来越多的数据表明滑膜和关节软骨都由这一群细胞发育而来。最后,关节软骨的发育通过位于关节表面的祖细胞/干细胞亚群驱动的附加生长而进行。骨骼的各个元件在称为关节或关节连接的区域连接在一起。传统上,关节有三大类:不动关节(纤维连结);运动范围有限的混合关节(微动关节);以及可动的或滑膜关节(滑膜关节)。本综述集中于滑膜关节的发育。

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