摘要
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The homeobox A (<i>HOXA</i>) family of genes is responsible for segmental development of the female reproductive tract during embryogenesis. However, <i>HOXA10</i> has been shown to be essential not only for uterus development, bu...
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The homeobox A (<i>HOXA</i>) family of genes is responsible for segmental development of the female reproductive tract during embryogenesis. However, <i>HOXA10</i> has been shown to be essential not only for uterus development, but also for implantation. Persistent expression and steroid-dependent regulation of this gene has been demonstrated in adult human, primate, murine and canine uteri. Moreover, <i>HOXA10</i>-dependent expression of prostaglandin H synthase-2 (PGHS-2), a key enzyme in prostaglandin production, has been previously detected. The role of the <i>HOXA10</i> gene in the porcine uterus is not well established. Therefore, the present studies were undertaken to (1) examine the effect of E<sub>2</sub> and P<sub>4</sub> on HOXA10 mRNA and protein content in the endometrium collected on day 9 of the estrous cycle and (2) determine the PGHS-2 protein expression and PGE<sub>2</sub> and PGF<sub>2 alpha </sub> secretion from endometrial tissue in response to steroid treatment. Endometrial explants collected from mature gilts on day 9 of the estrous cycle were incubated with E<sub>2</sub> (1-100 nM), P<sub>4</sub> (10-1000 nM) or E<sub>2</sub> (10 nM) and P<sub>4</sub> (100 nM) for 24 h. E<sub>2</sub> alone or E<sub>2</sub> in the presence of P<sub>4</sub> increased <i>HOXA10</i> mRNA expression in the endometrium (P<0.05). The HOXA10 protein level was upregulated in response to E<sub>2</sub>, P<sub>4</sub> and both steroids administered simultaneously (P<0.05). Moreover, E<sub>2</sub> and P<sub>4</sub> stimulated PGHS-2 protein expression in cultured endometrial explants. PGE<sub>2</sub>, but not PGF<sub>2 alpha </sub>, secretion increased in the presence of E<sub>2</sub> (P<0.05). However, the release of both prostaglandins was decreased after treatment of endometrial explants with the highest dose of P<sub>4</sub> (P<0.01). These results demonstrate that E<sub>2</sub> and P<sub>4</sub> are important regulators of <i>HOXA10</i> gene expression in the adult porcine endometrium during the mid-luteal phase of the estrous cycle. Additionally, the similar profiles of endometrial HOXA10 and PGHS-2 expression in the presence of E<sub>2</sub> and P<sub>4</sub> indicate that both genes are simultaneously regulated by steroids in the porcine uterus.
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