Opposite effects of osteogenic protein and transforming growth factor β on chondrogenesis in cultured long bone rudiments

• Published in: Journal of bone and mineral research Vol. 9; no. 6; pp. 771 - 780
• Main Authors: Dieudonné, S.C., Semeins, C.M., Goei, S.W., Vukicevic, S., Nulend, Klein J., Sampath, T.K., Helder, M., Burger, E.H.
• Format: Journal Article
• Language: English
• Published: Washington, DC John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR) 01-06-1994; American Society for Bone and Mineral Research
• Subjects: Animals; Biological and medical sciences; Bone Development - drug effects; Bone Morphogenetic Protein 7; Bone Morphogenetic Proteins; Calcium - metabolism; Cartilage - drug effects; Cartilage - embryology; Embryology: invertebrates and vertebrates. Teratology; Experimental organogenesis; Fundamental and applied biological sciences. Psychology; Glycosaminoglycans - metabolism; Humans; Metatarsal Bones - drug effects; Metatarsal Bones - embryology; Metatarsal Bones - metabolism; Mice; Organ Culture Techniques; Organogenesis. Physiological fonctions; Proteins - pharmacology; Recombinant Proteins - pharmacology; Transforming Growth Factor beta - pharmacology; Human; Embryonic development; Transforming growth factor β; Rodentia; Tissue culture; In vitro; Biological activity; Cartilage; Vertebrata; Mammalia; Bone morphogenetic protein; Mouse; Bone; Chondrogenesis; Comparative study; Osteogenesis
• ISSN: 0884-0431; 1523-4681
• DOI: 10.1002/jbmr.5650090603

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‐β1 and porcine TGF‐β1 and β2. Cartilage formation was determined by measurement of longitudinal growth of whole bone rudiments during culture and by the incorporation of 35SO4 into glycosaminoglycans. Mineralization was monitored by 45Ca 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‐β1 and β2 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.