Hashimoto Megumi, Nakasa Tomoyuki, Hikata Tomohiro, Asahara Hiroshi
Department of Regenerative Medicine, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-Ku, Tokyo 157-8535, Japan.
Med Res Rev. 2008 May;28(3):464-81. doi: 10.1002/med.20113.
This review article presents the current understanding of the molecular basis of articular cartilaginous homeostasis, and outlines potential areas to focus on within the developing field of therapeutics for cartilage disorders. Articular cartilage, an integral component of joints in extremities and the vertebral column, is essential for locomotion. Disturbance of joint development or cartilage homeostasis causes congenital osteocartilaginous dysplasia or osteoarthritic diseases, respectively. Symptomatic treatments and surgical replacement of joints are effective but can also be problematic in terms of quality of life over time. Recently, new insights into the molecular biological basis of chondrocyte differentiation and cartilage homeostasis have been reported. While joint formation is regulated by several growth factors such as Wnts (wingless-related MMTV integration site) and Gdfs (growth and differentiation factors), the pathology of osteoarthritis is now interpreted as the disruption of balance between anabolic and catabolic signals. Current findings in molecular biology on joint development are reviewed concisely to aid in the understanding of the molecular network that governs articular cartilage development and homeostasis.
这篇综述文章介绍了目前对关节软骨稳态分子基础的理解,并概述了在软骨疾病治疗这一发展中的领域内需要关注的潜在领域。关节软骨是四肢关节和脊柱的一个组成部分,对运动至关重要。关节发育紊乱或软骨稳态破坏分别导致先天性骨软骨发育不良或骨关节炎疾病。对症治疗和关节手术置换是有效的,但随着时间的推移,在生活质量方面也可能存在问题。最近,关于软骨细胞分化和软骨稳态分子生物学基础的新见解已有报道。虽然关节形成受多种生长因子如Wnts(无翅相关MMTV整合位点)和Gdfs(生长和分化因子)的调节,但骨关节炎的病理现在被解释为合成代谢和分解代谢信号之间平衡的破坏。本文简要综述了分子生物学在关节发育方面的当前研究结果,以帮助理解控制关节软骨发育和稳态的分子网络。