过氧化氢诱导条件下人黑素细胞树突变化及其胞内Ca2+浓度变化的研究
DOI:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:


Study on morphological alterations of dendrites and intracellular calcium concentration of human melanocytes induced by hydrogen perioxide
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:通过体外过氧化氢诱导模拟体内氧化压力条件下,联合观察人黑素细胞树突变化及其细胞内Ca2+浓度变化,初步说明黑素细胞经表皮丢失病理生理学基础-方法:采用常规分离培养人黑素细胞,分别用终浓度为0.1%和0.05%的H2O2作用于黑素细胞培养基中,于30-60-90-120和150 min后观察黑素细胞的树突变化,并通过目镜标尺测定树突变化率-另用Flu-3/AM染色,流式细胞术测定黑素细胞内钙离子荧光强度值-结果:使用不同浓度的H2O2诱导黑素细胞后树突显著回缩,0.1%H2O2对树突缩短作用强于0.05%H2O2;细胞内钙离子的荧光探针检测显示黑素细胞经过H2O2诱导后细胞内钙离子浓度升高,并且钙离子出现的峰值在诱导30 min时,早于黑素细胞树突缩短变化第1高峰60 min节点-结论:黑素细胞树突缩短可能与细胞内钙离子堆积,不能发生钙内流有关-

    Abstract:

    Objective: To elucidate pathophysiology of melanocytorrhagy by investigating morphological alterations of dendrites and intracellular calcium concentration(Ca2+) of human melanocytes induced by hydrogen perioxide(H2O2) in vitro. Methods:Melanocytes were cultured routinely, and 0.1% and 0.05% H2O2 were added to culture medium respectively. Dendrites’ length was observed at 30,60,90,120 and 150 min after treatment,and measured accurately by microscope optical ruler. Intracellular calcium was detected with Flu-3/AM probe by flow cytometry. Results:H2O2 induced a notable retraction of dendrites,of which concentration 0.1% had more potent effect than 0.05%. Intracellular calcium was up-regulated with the inducement of H2O2 detected by Flu-3/AM probe. Calcium peak presented was at 30 min after treatment, which is earlier than the first retraction peak of dendrites at 60 min. Conclusion:The results suggest retraction of dendrites might be related to accumulation of intracellular calcium, which led to failure of reflux of calcium.

    参考文献
    相似文献
    引证文献
引用本文

鲁 严,周梅华,吴 迪,王大光,朱 丰.过氧化氢诱导条件下人黑素细胞树突变化及其胞内Ca2+浓度变化的研究[J].南京医科大学学报(自然科学版),2011,(3):360-363

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2010-09-23
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期:
  • 出版日期:
通知关闭
郑重声明