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巨噬细胞集落刺激因子(M-CSF)与结缔组织生长因子/CCN2(CTGF/CCN2)在关节软骨细胞中的协同作用:对关节软骨代谢可能的再生作用

Collaborative action of M-CSF and CTGF/CCN2 in articular chondrocytes: possible regenerative roles in articular cartilage metabolism.

作者信息

Nakao Kyouji, Kubota Satoshi, Doi Hideyuki, Eguchi Takanori, Oka Morihiko, Fujisawa Takuo, Nishida Takashi, Takigawa Masaharu

机构信息

Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine and Dentistry, 2-5-1 Shikata-cho, Okayama 700-8525, Japan.

出版信息

Bone. 2005 May;36(5):884-92. doi: 10.1016/j.bone.2004.10.015. Epub 2005 Apr 7.

Abstract

It is known that expression of the macrophage colony-stimulating factor (M-CSF) gene is induced in articular chondrocytes upon inflammation. However, the functional role of M-CSF in cartilage has been unclear. In this study, we describe possible roles of M-CSF in the protection and maintenance of the articular cartilage based on the results of experiments using human chondrocytic cells and rat primary chondrocytes. Connective tissue growth factor (CTGF/CCN2) is known to be a potent molecule to regenerate damaged cartilage by promoting the growth and differentiation of articular chondrocytes. Here, we uncovered the fact that M-CSF induced the mRNA expression of the ctgf/ccn2 gene in those cells. Enhanced production of CTGF/CCN2 protein by M-CSF was also confirmed. Furthermore, M-CSF could autoactivate the m-csf gene, forming a positive feed-back network to amplify and prolong the observed effects. Finally, promotion of proteoglycan synthesis was observed by the addition of M-CSF. These findings taken together indicate novel roles of M-CSF in articular cartilage metabolism in collaboration with CTGF/CCN2, particularly during an inflammatory response. Such roles of M-CSF were further supported by the distribution of M-CSF producing chondrocytes in experimentally induced rat osteoarthritis cartilage in vivo.

摘要

已知巨噬细胞集落刺激因子(M-CSF)基因的表达在炎症发生时会在关节软骨细胞中被诱导。然而,M-CSF在软骨中的功能作用尚不清楚。在本研究中,我们基于使用人软骨细胞和大鼠原代软骨细胞的实验结果,描述了M-CSF在关节软骨保护和维持中的可能作用。已知结缔组织生长因子(CTGF/CCN2)是一种通过促进关节软骨细胞的生长和分化来再生受损软骨的有效分子。在此,我们发现M-CSF在这些细胞中诱导了ctgf/ccn2基因的mRNA表达。还证实了M-CSF增强了CTGF/CCN2蛋白的产生。此外,M-CSF可自激活m-csf基因,形成一个正反馈网络以放大和延长观察到的效应。最后,通过添加M-CSF观察到蛋白聚糖合成的促进作用。综合这些发现表明,M-CSF在与CTGF/CCN2协同作用的关节软骨代谢中具有新作用,特别是在炎症反应期间。M-CSF产生软骨细胞在实验诱导的大鼠骨关节炎软骨中的体内分布进一步支持了M-CSF的这种作用。

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