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山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (1): 21-26.doi: 10.6040/j.issn.1671-7554.0.2014.581

• 基础医学 • 上一篇    下一篇

四甲基吡啶卟啉-光动力疗法对人宫颈永生化上皮H8细胞的作用

宗丽菊1, 张友忠1, 王颉1, 吴淑霞1, 刘洪丽1, 张璐2   

  1. 1. 山东大学齐鲁医院妇产科, 山东 济南 250012;
    2. 兰州大学第一临床医学院, 甘肃 兰州 730000
  • 收稿日期:2014-09-05 修回日期:2014-10-29 发布日期:2015-01-10
  • 通讯作者: 张友忠。E-mail:zhangyouzhong@vip.sina.com E-mail:zhangyouzhong@vip.sina.com
  • 基金资助:
    国家自然科学基金(81072122)

Effects of TMPyP4-PDT on human immortal cervical epithelial H8 cells

ZONG Liju1, ZHANG Youzhong1, WANG Jie1, WU Shuxia1, LIU Hongli1, ZHANG Lu2   

  1. 1. Department of Gynecology and Obstetrics, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China;
    2. The First Clinical Medical College of Lanzhou University, Lanzhou 730000, Gansu, China
  • Received:2014-09-05 Revised:2014-10-29 Published:2015-01-10

摘要: 目的 探讨四甲基吡啶卟啉-光动力疗法(TMPyP4-PDT)对人宫颈永生化上皮H8细胞增殖和凋亡的影响。方法 显微镜下观察TMPyP4-PDT后H8细胞形态学变化;采用细胞活力试剂盒(CCK-8)检测细胞的增殖活力;Annexin V-FITC/PI双染试剂盒检测细胞凋亡率;免疫细胞化学SABC法检测TMPyP4-PDT对H8细胞p16INK4a蛋白的表达变化;蛋白免疫印迹法(Western blotting)检测人端粒酶逆转录酶(hTERT)、p21蛋白的表达。结果 TMPyP4-PDT可抑制H8细胞的增殖,诱导细胞凋亡,且在一定范围呈TMPyP4剂量依赖性;免疫细胞化学SABC法结果显示,TMPyP4-PDT可降低细胞p16INK4a蛋白的阳性率;Western blotting结果表明,TMPyP4-PDT下调 hTERT的表达,上调p21的表达。结论 TMPyP4-PDT可抑制H8细胞的增殖,诱导H8细胞的凋亡,其作用机制可能与下调p16INK4a、hTERT及上调p21的表达有关。

关键词: 四甲基吡啶卟啉-光动力疗法, H8细胞, 人端粒酶逆转录酶, p21蛋白, p16INK4a蛋白, 宫颈肿瘤

Abstract: Objective To investigate the effects of photosensitizer 5, 10, 15, 20-Tetrakis (1-methylpyridinium-4-yl) porphyrin based-photodynamic therapy (TMPyP4-PDT) on the proliferation and apoptosis of human immortal cervical epithelial H8 cells. Methods The morphological changes were observed by inverted microscope. Proliferative viability was evaluated with Cell Counting Kit-8. Apoptosis was assessed by Annexin V-FITC/PI Apoptosis Detection Kit. The p16INK4a expression was evaluated by immunocytochemistry Strept Avidin-Biotin-enzyme Complex (SABC) method. Human telomerase reverse transcriptase (hTERT) and p21 expression were analyzed by Western blotting. Results TMPyP4-PDT could inhibit H8 cellular proliferative viability and induce apoptosis in a TMPyP4 dose-dependent manner. Immunocytochemistry analysis revealed that TMPyP4-PDT could reduce the positive rate of p16INK4a protein in H8 cells. Western blotting results indicated that TMPyP4-PDT could downregulate hTERT protein expression while upregulate p21 protein in H8 cells. Conclusion TMPyP4-PDT can inhibit H8 cell proliferation and induce apoptosis. The possible mechanism is related to down-regulation of p16INK4a and hTERT, as well as up-regulation of p21 protein.

Key words: 5, 10, 15, 20-Tetrakis (1-methylpyridinium-4-yl) porphyrin- photodynamic therapy, p21 protein, Cervix neoplasms, H8 cells, Human telomerase reverse transcriptase, p16INK4a protein

中图分类号: 

  • R454.2
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