Andrology Center, First Hospital, Peking University, Beijing 100009, China.
Asian J Androl. 2010 Sep;12(5):744-52. doi: 10.1038/aja.2010.44. Epub 2010 Jul 26.
This study compared tankyrase 1 expression and autophagy quantity between erectile dysfunction (ED) and non-ED rats' corpus cavernosum smooth muscle cells (CSMCs). This study aslo explored the effect and possible mechanism of tankyrase 1 on autophagy and cell proliferation in ageing ED rats' CSMCs. The intracavernous pressure and mean systemic arterial pressure were measured to investigate erectile function so that eight 24-month-old ED and eight 8-month-old male Wistar rats were chosen respectively. The rat CSMCs were isolated and cultured by enzyme digestion, in which tankyrase 1 expression and autophagy quantity were compared. Tankyrase 1 overexpression was induced with plasmid transfection by Lipofectamine. The effect of tankyrase 1 overexpression on proliferation, autophagy and mTOR pathway in 24-month-old ED rats' CSMCs was measured by the cell growth curve in MTT assay, cell cycle analysis in flow cytometry (FCM), key protein expression in Western blot, autophagy quantity in transmission electron microscopy, monodansylcadaverine staining and GFP-LC3 fluorescence. The primary CSMCs were confirmed by immunofluorescence, and the purity was 99.1% in FCM. Compared with that of 8-month-old rats, tankyrase 1 expression and autophagy quantity significantly decreased in 24-month-old ED rats' primary CSMCs (P < 0.01). Tankyrase 1 overexpression significantly increased the growth rate (P < 0.05) and increased the S phase of cell cycle (P < 0.01). The autophagosome quantity was remarkably increased (P < 0.01), LC3-I/II and Beclin 1 were upregulated (P < 0.01 and P < 0.05), and p-p70S6K (Thr(389)) was downregulated in 24-month-old ED rat CSMCs (P < 0.05). In conclusion, Tankyrase 1 and autophagy decrease in the CSMCs from aging rats with ED, and tankyrase 1 may have a positive effect on proliferation by enhancing autophagy and regulating the mTOR signalling pathway.
本研究比较了勃起功能障碍(ED)和非 ED 大鼠海绵体平滑肌细胞(CSMC)中 tankyrase 1 的表达和自噬量。本研究还探讨了 tankyrase 1 对衰老 ED 大鼠 CSMC 中自噬和细胞增殖的影响及其可能机制。通过测量阴茎海绵体内压和平均系统动脉压来评估勃起功能,因此分别选择了 8 只 24 月龄的 ED 大鼠和 8 只 8 月龄的雄性 Wistar 大鼠。通过酶消化法分离培养大鼠 CSMC,比较 tankyrase 1 的表达和自噬量。通过脂质体转染质粒诱导 tankyrase 1 过表达。通过 MTT 比色法细胞生长曲线、流式细胞术(FCM)细胞周期分析、Western blot 关键蛋白表达、透射电镜观察自噬体数量、单丹磺酰尸胺染色和 GFP-LC3 荧光观察,测量 tankyrase 1 过表达对 24 月龄 ED 大鼠 CSMC 增殖、自噬和 mTOR 通路的影响。免疫荧光鉴定原代 CSMC,FCM 鉴定纯度为 99.1%。与 8 月龄大鼠相比,24 月龄 ED 大鼠原代 CSMC 中 tankyrase 1 的表达和自噬量明显降低(P < 0.01)。Tankyrase 1 过表达显著增加细胞生长速度(P < 0.05),并增加细胞周期的 S 期(P < 0.01)。自噬体数量显著增加(P < 0.01),LC3-I/II 和 Beclin 1 上调(P < 0.01 和 P < 0.05),p-p70S6K(Thr(389))下调(P < 0.05)。综上所述,ED 老年大鼠 CSMC 中 tankyrase 1 和自噬减少,tankyrase 1 可能通过增强自噬和调节 mTOR 信号通路对增殖产生积极影响。