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首页> 外文期刊>Developmental biology >Sonic hedgehog-patched Gli signaling in the developing rat prostate gland: lobe-specific suppression by neonatal estrogens reduces ductal growth and branching
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Sonic hedgehog-patched Gli signaling in the developing rat prostate gland: lobe-specific suppression by neonatal estrogens reduces ductal growth and branching

机译:发育中的大鼠前列腺中以音速刺猬修补的Gli信号:新生儿雌激素对肺叶的特异性抑制作用会减少导管的生长和分支

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While prostate gland development is dependent on androgens, other hormones including retinoids and estrogens can influence this process. Brief exposure to high-dose estrogen during the neonatal period in rats leads to permanent, lobe-specific aberrations in the prostate gland, a phenomenon referred to as developmental estrogenization.. We have previously shown that this response is mediated through alterations in steroid receptor expression;, however, further downstream mechanisms remain unclear. Herein, we examined Sonic hedgehog (Shh)-patched (ptc)-gli in the developing rat prostate gland, its role in branching morphogenesis, and the effects of neonatal estrogens on its expression and localization to determine whether a disturbance in this signaling pathway is involved in mediating the estrogenized phenotype. Shh was expressed in epithelial cells at the distal tips of elongating ducts in discreet, heterogeneous foci, while ptc and gli1-3 were expressed in the adjacent mesenchymal cells in the developing gland. The addition of Shh protein to cultured neonatal prostates reduced ductal growth and branching, decreased Fgf10 transcript, and increased Bmp4 expression in the adjacent mesenchyme. Shh-induced growth suppression was reversed by exogenous Fgf10, but not noggin, indicating that Fgf10 suppression is the proximate cause of the growth inhibition. A model is proposed to show how highly localized Shh expression along with regulation of downstream morphogens participates in dichotomous branching during prostate morphogenesis. Neonatal exposure to high-dose estradiol suppressed Shh, ptc, gli1, and gli3 expressions and concomitantly blocked ductal branching in the dorsal and lateral prostate lobes specifically. In contrast, ventral lobe branching and Shh-ptc-gli expression were minimally affected by estrogen exposure. Organ culture studies with lateral prostates confirmed that estradiol suppressed Shh-ptc-gli expression directly at the prostatic level. Taken together, the present findings indicate that lobe-specific decreases in Shh-ptc-gli expression are involved in mediating estradiol-induced suppression of dorsal and lateral lobe ductal growth and branching during prostate morphogenesis. (C) 2004 Elsevier Inc. All rights reserved.
机译:尽管前列腺的发育依赖于雄激素,但其他激素(包括类维生素A和雌激素)也会影响这一过程。在大鼠的新生儿期短暂暴露于高剂量雌激素会导致前列腺中永久性的,叶特异性畸变,这种现象称为发育雌激素化。我们以前已经表明,这种反应是通过类固醇受体表达的改变介导的;但是,进一步的下游机制仍不清楚。本文中,我们检查了发育中的大鼠前列腺中音速刺猬(Shh)修补的(ptc)-gli,其在分支形态发生中的作用以及新生雌激素对其表达和定位的影响,以确定该信号传导途径是否受到干扰参与介导雌激素表型。 Shh在离散的异质病灶的延长管末端的上皮细胞中表达,而ptc和gli1-3在发育腺的相邻间充质细胞中表达。 Shh蛋白添加到培养的新生儿前列腺中减少了导管的生长和分支,减少了Fgf10转录,并增加了相邻间充质中的Bmp4表达。 Shh诱导的生长抑制被外源Fgf10逆转,但noggin不能逆转,表明Fgf10抑制是生长抑制的最直接原因。提出了一个模型来显示在前列腺形态发生过程中高度定位的Shh表达以及下游形态发生因子的调控如何参与二分性分支。新生儿暴露于大剂量雌二醇会抑制Shh,ptc,gli1和gli3的表达,并特别地阻断了背侧和外侧前列腺叶的导管分支。相反,雌激素暴露对腹叶分支和Shh-ptc-gli表达的影响最小。前列腺侧面器官的培养研究证实,雌二醇直接在前列腺水平上抑制Shh-ptc-gli表达。两者合计,目前的发现表明,Shh-ptc-gli表达的叶特异性降低参与介导雌二醇诱导的前列腺形态发生过程中对背侧和旁叶导管的生长和分支的抑制。 (C)2004 Elsevier Inc.保留所有权利。

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