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Inhibitory effect of genistein on osteoclast-like cell formation in mouse marrow cultures
The effect of genistein on osteoclast-like cell formation in mouse marrow culture in vitro was investigated. The bone marrow cells were cultured for 7 days in α-minimal essential medium containing a well-known bone resorbing agent [parathyroid hormone (1–34) (PTH), prostaglandin E 2 (PGE 2), 1,25-di...
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Published in: | Biochemical pharmacology 1999-09, Vol.58 (5), p.767-772 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effect of genistein on osteoclast-like cell formation in mouse marrow culture
in vitro was investigated. The bone marrow cells were cultured for 7 days in α-minimal essential medium containing a well-known bone resorbing agent [parathyroid hormone (1–34) (PTH), prostaglandin E
2 (PGE
2), 1,25-dihydroxyvitamin D
3 (VD
3), or lipopolysaccharide (LPS)] with an effective concentration. Osteoclast-like cell formation was estimated by staining for tartrate-resistant acid phosphatase (TRACP), a marker enzyme of osteoclasts. The presence of PTH (10
−8 M), PGE
2 (10
−6 M), VD
3 (10
−8 M), or LPS (1 μg/mL) induced a remarkable increase in osteoclast-like multinucleated cells. These increases were inhibited significantly in the presence of genistein (10
−7 to 10
−5 M). The inhibitory effect of genistein (10
−5 M) was equal to that of 17 β-estradiol (10
−8 M), calcitonin (10
−9 M), or zinc sulfate (10
−5 M). Genistein (10
−5 M) significantly inhibited dibutyryl cyclic adenosine monophosphate (10
−5 M)-induced osteoclast-like cell formation. However, genistein (10
−5 M) did not inhibit phorbol 12-myristate 13-acetate-induced osteoclast-like cell formation. The present study demonstrated that genistein has a potent inhibitory effect on osteoclast-like cell formation in mouse marrow culture. The inhibitory action of genistein may involve in cyclic AMP signaling. |
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ISSN: | 0006-2952 1873-2968 |
DOI: | 10.1016/S0006-2952(99)00162-8 |