| First Author | Lindberg MK | Year | 2001 |
| Journal | J Endocrinol | Volume | 171 |
| Issue | 2 | Pages | 229-36 |
| PubMed ID | 11691642 | Mgi Jnum | J:72536 |
| Mgi Id | MGI:2153222 | Doi | 10.1677/joe.0.1710229 |
| Citation | Lindberg MK, et al. (2001) Estrogen receptor specificity in the regulation of the skeleton in female mice. J Endocrinol 171(2):229-36 |
| abstractText | There are two known estrogen receptors, estrogen receptor-alpha (ERalpha) and estrogen receptor-beta (ERbeta), which may mediate the actions of estrogen. The aim of the present study was to compare fat content, skeletal growth and adult bone metabolism in female mice lacking ERalpha (ERKO), ERbeta (BERKO) or both ERs (DERKO). We demonstrate that endogenous estrogens decrease the fat content in female mice via ERalpha and not ERbeta. Interestingly, the longitudinal bone growth was decreased in ERKO, increased in BERKO, but was intermediate in DERKO females, demonstrating that ERalpha and ERbeta exert opposing effects in the regulation of longitudinal bone growth. The effects on longitudinal bone growth were correlated with similar effects on serum levels of IGF-I. A complex regulation of the trabecular bone mineral density (BMD), probably caused by a disturbed feedback regulation of estrogen and testosterone, was observed in female ER-inactivated mice. Nevertheless, a partial functional redundancy for ERalpha and ERbeta in the maintenance of the trabecular BMD was observed in the female mice at 60 days of age. Thus, ERalpha and ERbeta may have separate effects (regulation of fat), opposing effects (longitudinal bone growth) or partial redundant effects (trabecular BMD at 60 days of age), depending on which parameter is studied. |
