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Opposite effects of osteogenic protein and transforming growth factor β on chondrogenesis in cultured long bone rudiments
Author(s) -
Dieudonné S.C.,
Semeins C.M.,
Goei S.W.,
Vukicevic S.,
Nulend Klein J.,
Sampath T.K.,
Helder M.,
Burger E.H.
Publication year - 1994
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650090603
Subject(s) - cartilage , chondrogenesis , chemistry , endocrinology , bone growth , medicine , glycosaminoglycan , bone morphogenetic protein , transforming growth factor , transforming growth factor beta , endochondral ossification , anatomy , biology , biochemistry , gene
Osteogenic protein‐1 (OP‐1, also called BMP‐7) is a bone morphogenetic member of the TGF‐β superfamily. In the present study, we examined the effect of recombinant human OP‐1 on cartilage and bone formation in organ cultures of metatarsal long bones of mouse embryos and compared the OP‐1 effects with those of human TGF‐β 1 and porcine TGF‐β 1 and β 2 . Cartilage formation was determined by measurement of longitudinal growth of whole bone rudiments during culture and by the incorporation of 35 SO 4 into glycosaminoglycans. Mineralization was monitored by 45 Ca incorporation in the acid‐soluble fraction and by measuring the length of the calcifying center of the rudiment. Toluidine blue‐stained histologic sections were used for quantitative histomorphometric analysis. We found that OP‐1 stimulated cartilage growth as determined by sulfate incorporation and that it increased remarkably the width of the long bones ends compared with controls. This effect was partly caused by differentiation of perichondrial cells into chondrocytes, resulting in increased appositional growth. In contrast to OP‐1, TGF‐β 1 and β 2 inhibited cartilage growth and reduced the length of whole bone rudiments compared with controls. In the ossifying center of the bone rudiments, both OP‐1 and TGF‐β inhibited cartilage hypertrophy, growth of the bone collar, and matrix mineralization. These data demonstrate that OP‐1 and TGF‐β exhibit opposite effects on cartilage growth but similar effects on osteogenesis in embryonic mouse long bone cultures. Since both OP‐1 and TGF‐β have been demonstrated in embryonic cartilage and bone, these results suggest that they act as autocrine or paracrine regulators of embryonic bone development.