›› 2002, Vol. 22 ›› Issue (3): 138-140.

• 论文 • 上一篇    下一篇

小鼠粗线期精母细胞钙离子通道膜片箝方法的建立

  

  1. 南京医科大学毒理学研究所神经毒理室,南京 210029
  • 收稿日期:2002-04-30 出版日期:2002-01-25 发布日期:2013-03-19
  • 基金资助:

    国家自然科学基金资助项目(30170811)

Study on Ca2++ Channels of Mouse Pachytene Spermatocytes Using Patch Clamp

  1. Nanjing Medical University,Nanjing 210029,China
  • Received:2002-04-30 Online:2002-01-25 Published:2013-03-19

摘要: 应用机械分离获得小鼠单个精母细胞,采用全细胞膜片箝技术记录Ca2++离子通道电流。结果表明:①阻断K+电流后,当钳制电位-90mV、指令电压-60~+10mV、步阶电压10mV时,可记录到内向电流;②内向电流在-30~-40mV达到最大值;③在细胞外液中加入4μmol/LTTX,对记录电流无影响,表明此电流不含有Na+电流成分,为Ca2++电流。

关键词: 精母细胞, 全细胞膜片箝技术, 钙离子通道

Abstract: Ca2+currents were obtained in acutely dissociated mouse spermatogenic cells using whole-cell patch clamp technique. The results indicated that inward currents were recorded when K+ currents were blocked by Cs+and TEA+stepping membrane potential to voltage between —80 and +10 mV,in 10 mV increments from a holding potential of —90 mV,the peak amplitude occurred at between —30 mV and —40 mV,and the inward currents remained unchanged in the presence of 4 μmol/L tetrodoxin (TTX),a special sodium channels blocker,suggesting that it was generated by opening Ca2+channels other than Na+channels.

Key words: Spermatocyte, Whole-cell patch clamp technique, Ca2+channels