Coexpression of ERβ with ERα and progestin receptor proteins in the female rat forebrain:: Effects of estradiol treatment
Coexpression of ERβ with ERα and progestin receptor proteins in the female rat forebrain:: Effects of estradiol treatment
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DOI:
10.1210/en.142.12.5172
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发表时间:
2001-12-01
期刊:
影响因子:
4.8
通讯作者:
Blaustein, JD
中科院分区:
文献类型:
--
作者:
Gréco, B;Allegretto, EA;Blaustein, JD
Estrogen and progestin receptors (ER, PgR) play a critical role in the regulation of neuroendocrine functions in females. The neuroanatomical distribution of the recently cloned, ER beta, overlaps with both Ella and PgR. To determine whether ER beta is found within ER alpha- or PgR-containing neurons in female rat, we used dual label immunocytochemistry. ER beta -immunoreactivity (ER beta -ir) was primarily detected in the nuclei of cells in the periventricular preoptic area (PvPO), the bed nucleus of the stria terminalis (BNSTpr), the paraventricular nucleus, the supraoptic nucleus, and the medial amygdala (MEApd). Coexpression of ER beta -ir with ER alpha -ir or PgR-ir was observed in the PvPO, BNSTpr, and MEApd in ovariectomized rats. E2 treatment decreased the number of ER beta -ir cells in the PvPO and BNSTpr and the number of ER alpha -ir cells in the MEApd and paraventricular nucleus, and therefore decreased the number of cells coexpressing ER beta -ir and ER alpha -ir in the PvPO, BNSTpr, and MEApd. E2 treatment increased the amount of PgR-ir in cells of the PvPO, BNSTpr, and MEApd, a portion of which also contained ER beta. These results demonstrate that ER beta is expressed in ER alpha- or PgR-containing cells, and they suggest that E can modulate the ratios of these steroid receptors in a brain region-specific manner.