Orr Brigid, Grace O Cathal, Vanpoucke Griet, Ashley George R, Thomson Axel A
Medical Research Council Human Reproductive Sciences Unit, Centre for Reproductive Biology, The Queen's Medical Research Institute, Little France Crescent, Edinburgh EH16 4TJ, United Kingdom.
Endocrinology. 2009 Jan;150(1):463-72. doi: 10.1210/en.2008-0383. Epub 2008 Sep 18.
Notch1 signaling is involved in epithelial growth and differentiation of prostate epithelia, and we have examined the role that notch signaling plays in the stroma of the developing prostate. We initially observed expression of delta-like 1 (Dlk1) and Notch2 in gene profiling studies of prostatic mesenchyme, and anticipated that they might be expressed in a key subset of inductive mesenchyme. Using quantitative RT-PCR, Northern blotting, and whole mount in situ hybridization, we confirmed that both Dlk1 and Notch2 mRNAs showed a restricted expression pattern within subsets of the stroma during prostate development. Localization of Dlk1 and Notch2 proteins mirrored the transcript expression, and showed both distinct and overlapping expression patterns within the stroma. Dlk1 and Notch2 were coexpressed in condensed inductive mesenchyme of the ventral mesenchymal pad (VMP), and were partially colocalized in the smooth muscle (SM) layer of the urethral stroma. In addition, Dlk1 was not expressed in SM adjacent to the VMP in female urethra. The function of notch signaling was examined using organ cultures of prostate rudiments and a small molecule inhibitor of notch receptor activity. Inhibition of notch signaling led to a loss of stromal tissue in both prostate and female VMP cultures, suggesting that this pathway was required for stromal survival. Inhibition of notch signaling also led to changes in both epithelial and stromal differentiation, which was evident in altered distributions of SM alpha-actin and p63 in prostates grown in vitro. The effects of notch signaling upon the stroma were only evident in the presence of testosterone, in contrast to effects upon epithelial differentiation.
Notch1信号通路参与前列腺上皮细胞的生长和分化,我们已经研究了Notch信号通路在发育中的前列腺基质中所起的作用。我们最初在前列腺间充质的基因谱研究中观察到delta样1(Dlk1)和Notch2的表达,并预计它们可能在诱导性间充质的一个关键亚群中表达。通过定量RT-PCR、Northern印迹和全组织原位杂交,我们证实Dlk1和Notch2 mRNA在前列腺发育过程中在基质亚群内呈现出受限的表达模式。Dlk1和Notch2蛋白的定位反映了转录本的表达,并在基质内显示出不同和重叠的表达模式。Dlk1和Notch2在腹侧间充质垫(VMP)的浓缩诱导性间充质中共表达,并在尿道基质的平滑肌(SM)层中部分共定位。此外,Dlk1在雌性尿道中与VMP相邻的SM中不表达。使用前列腺原基的器官培养物和Notch受体活性的小分子抑制剂来研究Notch信号通路的功能。Notch信号通路的抑制导致前列腺和雌性VMP培养物中的基质组织丢失,表明该通路是基质存活所必需的。Notch信号通路的抑制还导致上皮和基质分化的改变,这在体外培养的前列腺中平滑肌α-肌动蛋白和p63分布的改变中很明显。与对上皮分化的影响相反,Notch信号通路对基质的影响仅在睾酮存在的情况下才明显。