期刊文献+

Effect of tankyrase 1 on autophagy in the corpus cavernosum smooth muscle cells from ageing rats with erectile dysfunction and its potential mechanism 被引量:12

Effect of tankyrase 1 on autophagy in the corpus cavernosum smooth muscle cells from ageing rats with erectile dysfunction and its potential mechanism
下载PDF
导出
摘要 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 pres- sure 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 choosed respectively. The rat CSMCs were isolated and cultured by enzyme digestion, in which tankyrase 1 expression and autophagy quantity were compared. Tankyrase 1 over-expression was induced with plasmid transfection by Lipofectamine^TM. 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 (Thr389) 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. 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 pres- sure 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 choosed respectively. The rat CSMCs were isolated and cultured by enzyme digestion, in which tankyrase 1 expression and autophagy quantity were compared. Tankyrase 1 over-expression was induced with plasmid transfection by Lipofectamine^TM. 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 (Thr389) 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.
出处 《Asian Journal of Andrology》 SCIE CAS CSCD 2010年第5期744-752,共9页 亚洲男性学杂志(英文版)
基金 Acknowledgment We are grateful to Dr Tamotsu Yoshimori for providing the GFP-LC3 plasmid and Dr H. Seimiya for providing the tankyrase 1 plasmid. This study was supported by the National Natural Science Foundation of China (No. 30772285) and Beijing Municipal Commission of Science Technology, China (No. Z080507030808011).
关键词 ageing AUTOPHAGY corpora cavernosum corpus cavemosum smooth muscle cells erectile dysfunction SENILE TANKYRASE ageing, autophagy, corpora cavernosum, corpus cavemosum smooth muscle cells, erectile dysfunction, senile, tankyrase
  • 相关文献

参考文献3

二级参考文献17

  • 1Wu-Jiang Liu Zhong-Cheng Xin Hua Xin Yi-Ming Yuan Long Tian Ying-Lu Guo.Effects of icariin on erectile function and expression of nitric oxide synthase isoforms in castrated rats[J].Asian Journal of Andrology,2005,7(4):381-388. 被引量:23
  • 2吴小军,辛钟成,朱一辰,李东辉,高 冰.正义Tankyrase转染大鼠海绵体平滑肌细胞的作用研究[J].中国男科学杂志,2006,20(9):17-20. 被引量:2
  • 3蒋兆健,胡本容,付琴,汤强,向继洲,刘菊妍.淫羊藿苷对家兔阴茎海绵体环核苷酸水平的影响[J].华中科技大学学报(医学版),2007,36(2):166-168. 被引量:16
  • 4吴晓军 张家华 金锡御.增龄及喂养L—精氨酸对大鼠阴茎组织NOS活性的影响[J].中华泌尿外科杂志,1999,20(6):331-331.
  • 5Monga M.The aging penis:erectile dysfunction.Geriatr Nephrol Urol 1999; 9(1):27-37
  • 6吴晓军 张家华 金锡御.不同月龄大鼠阴茎组织一氧化氮及内皮素的变化[J].中华泌尿外科杂志,1999,20(7):418-418.
  • 7Bakircioglu ME,Sievert KD,Nunes L,et al.Decreased trabecular smooth muscle and caveolin-1 expression in the penile tissue of aged rats.J Urol 2001; 166(2):734-738
  • 8Smith S,Giriat I,Schmitt A,et al.Tankyrase,a poly (ADP-ribose) polymerase at human telomeres.Science 1998; 282(5393):1484-1487
  • 9金冬雁,黎孟枫等译.《分子克隆实验指南》.北京:第二版:科学出版社,1993
  • 10McCullough AR,Barada JH,Fawzy A.Achieving treatment optimization with sildenafil citrate (Viagra) in patients with erectile dysfunction.Urology 2002; 60(2 Suppl 2):28-38

共引文献16

同被引文献62

引证文献12

二级引证文献46

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部