Hetzl Amanda Cia, Montico Fabio, Kido Larissa Akemi, Cagnon Valéria Helena Alves
Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Structural and Cellular Biology Postgraduate Program, Brazil.
Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Structural and Cellular Biology Postgraduate Program, Brazil.
Tissue Cell. 2016 Jun;48(3):189-96. doi: 10.1016/j.tice.2016.03.008. Epub 2016 Mar 19.
The aim of this study was to characterize and relate the prolactin (PR), epidermal growth factor receptor (EGFR), α-actin and vimentin immunoreactivity in the prostate of elderly rats subjected to steroid hormonal imbalance. Senile and young rats were divided into the young group (YNG), the senile group (SE), the castrated group (CAS), the estrogen-deficient group (ED), the castrated+estrogen group (CASE), and the estrogen-deficient+androgen group (EDTEST). PR and EGFR increased in the estrogen and androgen ablation groups. In addition, EGFR influenced the immunolocalization by changing it from the prostatic stroma to the epithelium in elderly rats. Hormone ablation in elderly rats, not only related to androgen but also estrogen, led to increased stromal EGFR immunolocalization. The α-actin pattern decreased in the groups with estrogenic imbalance. Moreover, vimentin increased in the senile and estrogen deficient group. To conclude, we can suggest that EGFR contributed towards the proliferative process in the prostate, by means however, of different mechanisms, considering the androgenic and estrogenic pathways. Also, our results indicated that prolactin could be activated not only in an androgen-independent pathway but also in an estrogen independent pathway. Finally, PR and vimentin immunolocalization increase, in the prostatic stroma in the group showing estrogenic ablation, could be one of the factors which contribute to the reactive stroma formation.
本研究的目的是对遭受类固醇激素失衡的老年大鼠前列腺中的催乳素(PR)、表皮生长因子受体(EGFR)、α-肌动蛋白和波形蛋白免疫反应性进行表征并建立联系。将老年和年轻大鼠分为年轻组(YNG)、老年组(SE)、去势组(CAS)、雌激素缺乏组(ED)、去势+雌激素组(CASE)以及雌激素缺乏+雄激素组(EDTEST)。在雌激素和雄激素切除组中,PR和EGFR增加。此外,EGFR通过改变老年大鼠前列腺基质到上皮的免疫定位来影响免疫定位。老年大鼠的激素切除不仅与雄激素有关,还与雌激素有关,导致基质EGFR免疫定位增加。在雌激素失衡组中,α-肌动蛋白模式减少。此外,波形蛋白在老年和雌激素缺乏组中增加。总之,我们可以认为,考虑到雄激素和雌激素途径,EGFR通过不同机制对前列腺的增殖过程有促进作用。此外,我们的结果表明,催乳素不仅可以在雄激素非依赖途径中被激活,还可以在雌激素非依赖途径中被激活。最后,在雌激素切除组的前列腺基质中PR和波形蛋白免疫定位增加,可能是促成反应性基质形成的因素之一。