Hetzl A C, Montico F, Lorencini R M, Kido L A, Cândido E M, Cagnon V H A
Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), P.O. Box 6109, Campinas, SP, 13083-865, Brazil.
Histochem Cell Biol. 2014 May;141(5):531-42. doi: 10.1007/s00418-013-1173-y. Epub 2013 Dec 22.
The aim was to characterize and correlate steroid hormone receptors with the FGF2, FGF7 and FGF8 reactivities in the prostatic epithelium and stroma in senile rats. Fifty male senile rats and 10 young male rats were divided into the young (YNG), the senile groups (SE), the castrated group (CAS), the estrogen-deficient group (ED), the castrated + estrogen group (CASE), and the estrogen-deficient + androgen group (EDTEST). The ventral prostate was submitted to immunohistochemical and Western blotting analyses. The results showed decreased AR and ERβ levels and increased ERα in the senile animals in relation to YNG group. Increased ERα and ERβ reactivities presenting differential localization were characterized in the CASE group compared to the CAS group. Increased FGF2 level was observed in the stroma of the CAS and ED groups in relation to the SE group and in the epithelium of the ED group in relation to the other groups. Increased and differential immunolocalization of FGF7 levels were observed in the CAS, ED and CASE groups. The FGF8 levels showed differential localization in the CAS and ED groups compared to the senile group. The intense hormone ablation was favorable to the autocrine signaling of FGF2 and FGF8. FGF7 could be activated in the androgen-independent via considering the increased FGF7 in the castrated rats. We concluded that hormone ablation in senescence was favorable to activation or/and to fibroblast signaling in the prostatic microenvironment.
目的是在老年大鼠的前列腺上皮和基质中,对类固醇激素受体进行表征,并将其与FGF2、FGF7和FGF8的反应性相关联。将50只雄性老年大鼠和10只年轻雄性大鼠分为年轻组(YNG)、老年组(SE)、去势组(CAS)、雌激素缺乏组(ED)、去势+雌激素组(CASE)和雌激素缺乏+雄激素组(EDTEST)。对腹侧前列腺进行免疫组织化学和蛋白质印迹分析。结果显示,与YNG组相比,老年动物体内AR和ERβ水平降低,ERα升高。与CAS组相比,CASE组中ERα和ERβ反应性增加且呈现不同定位。与SE组相比,CAS组和ED组基质中FGF2水平升高,与其他组相比,ED组上皮中FGF2水平升高。在CAS、ED和CASE组中观察到FGF7水平增加且免疫定位不同。与老年组相比,CAS组和ED组中FGF8水平呈现不同定位。强烈的激素去除有利于FGF2和FGF8的自分泌信号传导。考虑到去势大鼠中FGF7增加,FGF7可能在雄激素非依赖性途径中被激活。我们得出结论,衰老过程中的激素去除有利于前列腺微环境中激活或/和成纤维细胞信号传导。