Bone morphogenetic protein 2 increases insulin-like growth factor I and II transcripts and polypeptide levels in bone cell cultures
Open Access
- 1 December 1994
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Bone and Mineral Research
- Vol. 9 (12) , 1999-2005
- https://doi.org/10.1002/jbmr.5650091221
Abstract
Insulin-like growth factors (IGF) I and II are among the most prevalent growth factors secreted by bone cells and are presumed to act as autocrine regulators of bone formation. Certain growth factors, synthesized by skeletal cells and known to stimulate the replication but not the differentiated function of cells of the osteoblastic lineage, have been shown to inhibit skeletal IGF-I and II synthesis. We postulated that growth factors with limited mitogenic activity and with differentiation-inducing properties, such as bone morphogenetic protein (BMP) 2, have the opposite effect and enhance IGF-I and II synthesis. We tested the effects of BMP-2 on IGF-I and II mRNA expression and polypeptide concentrations in cultures of osteoblast-enriched (OB) cells from 22 day fetal rat calvariae. Steady-state IGF-I and II mRNA levels were determined by northern blot analysis, and IGF-I and II concentrations were determined in acidified and fractionated culture medium by a specific radioimmunoassay. After 24-48 h of treatment, BMP-2 at 3.3 nM increased IGF-I and II transcripts by up to twofold and polypeptide levels by up to fourfold. BMP-2 was a more potent stimulator of IGF-II synthesis, and it was active at doses as low as 0.03 nM for IGF-II mRNA and 0.3 nM for IGF-II protein, whereas a dose of 3.3 nM was required to observe the effect on IGF-I synthesis. The effects of BMP-2 on IGF-I and II transcripts and polypeptide levels were dependent on protein synthesis and decreased in the presence of cycloheximide at 3.6 μM. In conclusion, BMP-2 increases skeletal IGF-I and II synthesis by increasing IGF-I and II transcript levels, and this effect may contribute to its actions on selected aspects of OB cell differentiated function.Keywords
Funding Information
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 42424, DK 45227)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases. (AR 21707)
This publication has 38 references indexed in Scilit:
- Expression of Bone Morphogenic Protein 7 mRNA in MDCK CellsBiochemical and Biophysical Research Communications, 1993
- Biosynthesis and in vivo localization of the decapentaplegic-Vg-related protein, DVR-6 (bone morphogenetic protein-6).The Journal of cell biology, 1993
- Bone morphogenetic proteins (BMP-2 and BMP-3) promote growth and expression of the differentiated phenotype of rabbit chondrocytes and osteoblastic MC3T3-E1 cells in vitroJournal of Bone and Mineral Research, 1991
- Bone morphogenetic protein-2b stimulation of growth and osteogenic phenotypes in rat osteoblast-like cells: Comparison with TGF-β1Journal of Bone and Mineral Research, 1991
- Relative binding and biochemical effects of heterodimeric and homodimeric isoforms of platelet‐derived growth factor in osteoblast‐enriched cultures from fetal rat boneJournal of Cellular Physiology, 1991
- Bone morphogenetic protein-2 stimulates alkaline phosphatase activity and collagen synthesis in cultured osteoblastic cells, MC3T3-E1Biochemical and Biophysical Research Communications, 1991
- Novel Regulators of Bone Formation: Molecular Clones and ActivitiesScience, 1988
- Primary structure of human skeletal growth factor: homology with human insulin-like growth factor-IIBiochimica et Biophysica Acta (BBA) - General Subjects, 1988
- Effects of bone associated growth factors on dna, collagen and osteocalcin synthesis in cultured fetal rat calvariaeBone, 1988
- Comparing the Means of Several GroupsNew England Journal of Medicine, 1985