›› 2009, Vol. 40 ›› Issue (2): 223-227.doi: 10.3969/j.issn.0529-1356.2009.02. 011

• 论著 • 上一篇    下一篇

姜黄素诱导永生化人HaCaT细胞凋亡

杨海波1 ;李祺福1* ;石松林1 ;李钟洙2 ;宋建晔1 ;刘用金1   

  1. 1.厦门大学生命科学学院 教育部细胞生物学与肿瘤细胞工程重点实验室,福建 厦门 361005;2.厦门市第一医院皮肤科,福建 厦门 361005
  • 收稿日期:2007-12-24 修回日期:2008-03-09 出版日期:2009-04-06
  • 通讯作者: 李祺福

Curcumin induces apoptosis of immortalized human epithelial cell line HaCaT

  1. 1.Laboratory of Cell Biology, Key Laboratory of Ministry of Education for Cell Biology and Tumor Cell Engineering,School of Life Sciences,Xiamen University, Fujian Xiamen 361005, China;2.Department of Derma Laboratory,the First Hospital of Xiamen, Fujian Xiamen 361005, China
  • Received:2007-12-24 Revised:2008-03-09 Online:2009-04-06
  • Contact: LI Qi-fu

关键词: 姜黄素, 上皮细胞, 流式细胞术, 琼脂糖凝胶电泳

Abstract: Objective To study the apoptosis effect of curcumin(Cur) on the immortalized human epithelial cell line HaCaT. Methods The apoptosis effect were detected cell by cell count, flow cytometry analysis, DNA gel electrophoresis, Hoechst33258 staining,HE staining, and electron microscopy. Results After treated with 7.5mg/L curcumin the proliferation of HaCaT cells were inhibited, and the inhibitory rate was 83.03%. The results of flow cytometry analysis showed that curcumin could induced the emergence of the phase of apoptosis, and the rate was 13.1%,the cell cycle were arrested in GSUB>2/SUB>/M phase. Agarose gel electrophoresis revealed that cell DNA fragment exhibited characteristic “DNA ladder”. Cell nucleus concentrated and appeared granular fluorescence by Hoechst33258 staining. Light microscope and electron microscope showed that the cells treated with curcumin shrinked, cell nucleus concerntrated.chromatin agglutinated, mitochondria swelled, and apoptosis body formed. Conclusion This study suggests that curcumin could induce apoptosis of immortalized human epithelial cell line HaCaT effectively, and provided an important foundation for further studying the consenescence and apoptosis mechanisms of the epid

Key words: Curcumin, Epidermis cell, Flow cytometry, DNA gel electrophoresis

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