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蝾螈美西螈输卵管纤毛活动的钙依赖性

Calcium dependence of ciliary activity in the oviduct of the salamander Necturus.

作者信息

Eckert R, Murakami A

出版信息

J Physiol. 1972 Nov;226(3):699-711. doi: 10.1113/jphysiol.1972.sp010004.

DOI:10.1113/jphysiol.1972.sp010004
PMID:4637627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1331171/
Abstract
  1. Ciliary activity in the oviduct of the mud puppy Necturus maculosus was monitored by a photometric technique in normal, decalcified, and Triton X-extracted preparations to investigate the regulatory role of calcium ions.2. The frequency of ciliary beating in the isolated tissue ranged from 0 to 12 beats/sec. The frequency in any one group of cells underwent large cyclical variations with periods of 2 min or more.3. Frequency of beating reached a maximum and remained at a plateau upon addition of 1 mM caffeine. Beating temporarily ceased upon removal of the caffeine.4. Ionophoretic injection of calcium ions into an active cell bathed in Ringer solution produced an increased rate of beating. In cells rendered quiescent by prior decalcification with EGTA, injected calcium rapidly restored ciliary activity.5. Epithelia extracted in Triton X-100 were inactive until reactivated by addition of ATP and magnesium ions. The frequency of beating increased between 0.1 and 4.0 mM ATP in 1 mM magnesium, and between 0.2 and 2.5 mM magnesium in 1 mM ATP.6. The frequency of beating in the ATP-reactivated, Triton-extracted tissue was independent of the calcium ion concentration.7. Cells inactivated by decalcification were reactivated by injection of ATP or by extracellular ATP levels as low as 3 x 10(-8)M.8. It is concluded that the frequency of beating depends directly on the concentration of the available energy source, presumably ATP, and that an indirect dependence of beating frequency on calcium concentration in the living tissue results from rate-limiting effects of intracellular calcium on metabolic steps in pathways leading to ATP synthesis.
摘要
  1. 运用光度测定技术,在正常、脱钙及经 Triton X 处理的美西螈输卵管制剂中监测纤毛活动,以研究钙离子的调节作用。

  2. 分离组织中纤毛摆动频率为 0 至 12 次/秒。任何一组细胞的频率都经历 2 分钟或更长时间的大幅周期性变化。

  3. 添加 1 mM 咖啡因后,摆动频率达到最大值并保持稳定。去除咖啡因后,摆动暂时停止。

  4. 向浸浴在林格氏液中的活跃细胞进行离子电泳注射钙离子,可使摆动速率增加。在用 EGTA 预先脱钙而静止的细胞中,注入的钙离子能迅速恢复纤毛活动。

  5. 用 Triton X - 100 提取的上皮细胞无活性,直到添加 ATP 和镁离子后重新激活。在 1 mM 镁存在下,ATP 浓度在 0.1 至 4.0 mM 之间时,摆动频率增加;在 1 mM ATP 存在下,镁离子浓度在 0.2 至 2.5 mM 之间时,摆动频率增加。

  6. 在 ATP 重新激活的、经 Triton 处理的组织中,摆动频率与钙离子浓度无关。

  7. 因脱钙而失活的细胞,通过注射 ATP 或细胞外低至 3×10⁻⁸M 的 ATP 水平可重新激活。

  8. 得出结论:摆动频率直接取决于可用能量源(可能是 ATP)的浓度,而在活体组织中,摆动频率对钙浓度的间接依赖是由于细胞内钙对导致 ATP 合成途径中代谢步骤的限速作用。

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