Shi Yun-Feng, Yu Dian-Jun, Jiang Chen-Yi, Wang Xing-Jie, Zhu Yi-Ping, Zhao Rui-Zhe, Lv Zhong, Sun Xiao-Wen
Department of Urology, Shanghai General Hospital of Nanjing Medical University, Shanghai, China.
Department of Urology, Wujin Hospital Affiliated Jiangsu University, Changzhou, China.
Prostate. 2018 Feb;78(3):193-201. doi: 10.1002/pros.23456. Epub 2017 Nov 23.
Increased prostatic smooth muscle tone and hyperplastic growth contribute to urethral obstruction and voiding symptoms in benign prostatic hyperplasia (BPH). It has been suggested that different proliferative potential of stromal cells between transition zone (TZ) and adjoining regions of the prostate plays a significant role in the development of BPH. However, the molecular mechanisms of this hyperplastic process remain unclear. We found tumor necrosis factor receptor-associated factor 6 (TRAF6) highly expressed in TZ stromal cells compared to peripheral zone (PZ) stromal cells by gene array analyzes. Therefore, we aim to study the potential mechanisms of stromal TRAF6 in promoting BPH progression.
Stromal cells obtained from BPH-derived primary cultures. The TRAF6-siRNA vector were constructed and transfected into cultured human BPH primary TZ stromal cells, and TRAF6-overexpressing vector were constructed and transfected into cultured human BPH primary PZ stromal cells. Stromal cells were recombined with BPH-1 cells then subcutaneously inoculated into the kidney capsule of male nude mice. Cell proliferation was evaluated by CCK-8 assay. Multiple proteins in the Akt/mTOR pathway were assessed using western blot.
TRAF6 levels were increased in TZ stroma compared with PZ stroma of BPH. The in vitro cell culture and in vivo cell recombination revealed that selective downregulation of TRAF6 in TZ stromal cells led to suppression of the proliferation, while upregulation of TRAF6 in PZ stromal cells enhanced the proliferation. We found that the Phosphorylation and Ubiquitination of Akt as well as the Phosphorylation of mTOR, P70 were decreased when TRAF6 was downregulated in primary cultured TZ stromal cells of BPH.
TRAF6 can promote the proliferation of stromal cells of BPH via Akt/mTOR signaling. Our results may make stromal TRAF6 responsible for zonal characteristic of BPH and as a promising therapeutic strategy for BPH treatment.
前列腺平滑肌张力增加和增生性生长导致良性前列腺增生(BPH)患者出现尿道梗阻和排尿症状。有研究表明,前列腺移行区(TZ)和相邻区域的基质细胞增殖潜能不同,在BPH的发生发展中起重要作用。然而,这种增生过程的分子机制尚不清楚。通过基因芯片分析,我们发现与外周区(PZ)基质细胞相比,肿瘤坏死因子受体相关因子6(TRAF6)在TZ基质细胞中高表达。因此,我们旨在研究基质TRAF6促进BPH进展的潜在机制。
从BPH原代培养物中获取基质细胞。构建TRAF6-siRNA载体并转染至培养的人BPH原代TZ基质细胞,构建TRAF6过表达载体并转染至培养的人BPH原代PZ基质细胞。将基质细胞与BPH-1细胞重组,然后皮下接种到雄性裸鼠的肾包膜。通过CCK-8法评估细胞增殖。使用蛋白质印迹法评估Akt/mTOR通路中的多种蛋白质。
与BPH的PZ基质相比,TZ基质中TRAF6水平升高。体外细胞培养和体内细胞重组显示,TZ基质细胞中TRAF6的选择性下调导致增殖受到抑制,而PZ基质细胞中TRAF6的上调增强了增殖。我们发现,在BPH原代培养的TZ基质细胞中,当TRAF6下调时,Akt的磷酸化和泛素化以及mTOR、P70的磷酸化均降低。
TRAF6可通过Akt/mTOR信号促进BPH基质细胞增殖。我们的结果可能使基质TRAF6成为BPH区域特征的原因,并成为BPH治疗的一种有前景的治疗策略。