Angiotensin II is generated from angiotensin I by bone cells and stimulates osteoclastic bone resorption in vitro

• Published in: Journal of endocrinology Vol. 152; no. 1; pp. 5 - 10
• Main Authors: HATTON, R, STIMPEL, M, CHAMBERS, T. J
• Format: Journal Article
• Language: English
• Published: Colchester BioScientifica 01.01.1997; Portland Press
• Subjects: Angiotensin I - metabolism; Angiotensin II - metabolism; Angiotensin II - pharmacology; Animals; Biological and medical sciences; Bone Resorption - chemically induced; Cattle; Cells, Cultured; Coculture Techniques; Dose-Response Relationship, Drug; Fundamental and applied biological sciences. Psychology; Mice; Mice, Inbred CBA; Osteoblasts - metabolism; Osteoclasts - metabolism; Rats; Rats, Wistar; Skeleton and joints; Stimulation, Chemical; Vertebrates: osteoarticular system, musculoskeletal system; Endothelial cell; Rat; Rodentia; Resorption; Stimulation; Osteoclast; In vitro; Osteoarticular system; Renin angiotensin system; Vertebrata; Mammalia; Hormonal regulation; Bone; Angiotensin II
• DOI: 10.1677/joe.0.1520005
• ISSN: 0022-0795

Abstract During bone resorption, osteoclasts are closely associated with endothelial cells. The latter are able to produce several agents that regulate bone resorption. In view of the increasing evidence that angiotensin II, which can be generated by endothelial cells, has actions outside the traditional renin-angiotensin system, we tested the effect of angiotensin II on bone resorption. Angiotensin II showed no effect either on osteoclast formation or on bone resorption by isolated osteoclasts. However, in co-cultures of osteoclasts with calvarial or MC3T3-E1 osteoblastic cells, and in osteoclastic cultures co-cultured with other bone cells obtained by prolonged sedimentation, angiotensin II stimulated bone resorption to a similar degree to that observed with 1,25(OH)2 vitamin D3. Stimulation of resorption was noted at concentrations of 10−7 m and above. We found that angiotensin I also stimulated bone resorption in co-cultures of osteoclasts with osteoblastic cells, and that this action was inhibited by inhibitors of angiotensin-converting enzyme. These results identify angiotensin I and II as potent stimulators of osteoclastic bone resorption, and raise the possibility that bone might contain a tissue-renin-angiotensin system that might play a role in the regulation of bone resorption. Journal of Endocrinology (1997) 152, 5–10