软骨发生
阿格里坎
软骨膜
化学
II型胶原
软骨细胞
细胞生物学
骨形态发生蛋白2
细胞外基质
软骨
转化生长因子β
骨膜
分子生物学
内科学
转化生长因子
生物
干细胞
解剖
体外
骨关节炎
病理
医学
生物化学
替代医学
关节软骨
作者
Keigo Hanada,Luis A. Solchaga,Arnold I. Caplan,Thomas M. Hering,Victor M. Goldberg,Jung U. Yoo,Brian Johnstone
标识
DOI:10.1002/1097-4644(20010501)81:2<284::aid-jcb1043>3.0.co;2-d
摘要
Periosteum contains osteochondral progenitor cells that can differentiate into osteoblasts and chondrocytes during normal bone growth and fracture healing. TGF-β1 and BMP-2 have been implicated in the regulation of the chondrogenic differentiation of these cells, but their roles are not fully defined. This study was undertaken to investigate the chondrogenic effects of TGF-β1 and BMP-2 on rat periosteum-derived cells during in vitro chondrogenesis in a three-dimensional aggregate culture. RT-PCR analyses for gene expression of cartilage-specific matrix proteins revealed that treatment with BMP-2 alone and combined treatment with TGF-β1 and BMP-2 induced time-dependent mRNA expression of aggrecan core protein and type II collagen. At later times in culture, the aggregates treated with BMP-2 exhibited expression of type X collagen and osteocalcin mRNA, which are markers of chondrocyte hypertrophy. Aggregates incubated with both TGF-β1 and BMP-2 showed no such expression. Treatment with TGF-β1 alone did not lead to the expression of type II or X collagen mRNA, indicating that this factor itself did not independently induce chondrogenesis in rat periosteal cells. These data were consistent with histological and immunohistochemical results. After 14 days in culture, BMP-2-treated aggregates consisted of many hypertrophic chondrocytes within a metachromatic matrix, which was immunoreactive with anti-type II and type X collagen antibodies. In contrast, at 14 days, TGF-β1+BMP-2-treated aggregates did not contain any morphologically identifiable hypertrophic chondrocytes and their abundant extracellular matrix was not immunoreactive to the anti-type X collagen antibody. Expression of BMPR-IA, TGF-β RI, and TGF-β RII receptors was detected at all times in each culture condition, indicating that the distinct responses of aggregates to BMP-2, TGF-β1 and TGF-β1+BMP-2 were not due to overt differences in receptor expression. Collectively, our results suggest that BMP-2 induces neochondrogenesis of rat periosteum-derived cells, and that TGF-β1 modulates the terminal differentiation in BMP-2 induced chondrogenesis. J. Cell. Biochem. 80:284–294, 2001. © 2001 Wiley-Liss, Inc.
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