Anabolic Effects of 1,25-Dihydroxyvitamin D3 on Osteoblasts Are Enhanced by Vascular Endothelial Growth Factor Produced by Osteoblasts and by Growth Factors Produced by Endothelial Cells*
| Autor: | Masakazu Miura, Da Shen Wang, Kanji Sato, Hiroshi Demura |
|---|---|
| Rok vydání: | 1997 |
| Předmět: |
Vascular Endothelial Growth Factor A
medicine.medical_specialty Anabolism medicine.medical_treatment Endothelial Growth Factors Models Biological Umbilical vein chemistry.chemical_compound Endocrinology Calcitriol Internal medicine medicine Humans Receptors Growth Factor Endothelin-2 Endothelin-3 Lymphokines Osteoblasts Endothelin-1 biology Vascular Endothelial Growth Factors Growth factor Receptor Protein-Tyrosine Kinases Alkaline Phosphatase Endothelin 1 Coculture Techniques Vascular endothelial growth factor Vascular endothelial growth factor A Receptors Vascular Endothelial Growth Factor chemistry Receptors Mitogen cardiovascular system biology.protein Endothelium Vascular Antibody Thymidine |
| Zdroj: | Endocrinology. 138:2953-2962 |
| ISSN: | 1945-7170 0013-7227 |
| DOI: | 10.1210/endo.138.7.5275 |
| Popis: | Human osteoblast-like cells (HOB) produce vascular endothelial growth factor (VEGF), the steady state level of which is stimulated by 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3]. As osteoblasts and endothelial cells are proximally located in skeletal tissue, we investigated the anabolic effects of 1,25-(OH)2D3 and VEGF on HOB cocultured with endothelial cells. When HOB with high alkaline phosphatase (Al-P) activity and human umbilical vein endothelial cells (HUVEC) with little activity were cultured together, Al-P activity increased, accompanied by an increase in cell number. When HOB and HUVEC were cultured separately, 1,25-(OH)2D3 did not directly stimulate [3H]thymidine incorporation into HUVEC, but stimulated it in the presence of HOB. VEGF did not directly stimulate the Al-P activity of HOB but stimulated it in the presence of HUVEC. The conditioned medium of HOB stimulated the proliferation of HUVEC, and this was partially blocked by anti-VEGF antibody. Conversely, the conditioned medium of HUVEC increased Al-P activity and [3H]thymidine incorporation into HOB, and this was partially blocked by antiinsulin-like growth factor I antibody and BQ-123, a specific antagonist of the endothelin-1 (ET-1) receptor. 1,25-(OH)2D3 stimulated the release of VEGF and ET-1 from HOB and HUVEC, respectively. Furthermore, the 1,25-(OH)2D3-induced release of VEGF was enhanced in HOB cocultured with HUVEC. A quantitative reverse transcription-PCR study revealed that genes for VEGF receptors (Flt-1 and KDR) were expressed in HUVEC, but not in HOB, and that 1,25-(OH)2D3 increased the levels of expression of VEGF receptor genes in endothelial cells only when cocultured with HOB. In summary, we demonstrated that 1,25-(OH)2D3 exerts an anabolic effect on osteoblasts by enhancing their production of VEGF, which stimulates its receptors on endothelial cells, followed by increased production of osteotropic growth factors, such as insulin-like growth factor I and ET-1. These in vitro findings suggest that the VEGF/VEGF receptor system may be involved in both bone formation and bone remodeling in vivo. |
| Databáze: | OpenAIRE |
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