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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Lysophospholipids induce membrane hyperpolarization in microglia by activation of IKCa1 Ca(2+)-dependent K(+) channels.
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Lysophospholipids induce membrane hyperpolarization in microglia by activation of IKCa1 Ca(2+)-dependent K(+) channels.

机译:溶血磷脂通过激活IKCa1 Ca(2+)依赖的K(+)通道,诱导小胶质细胞膜超极化。

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Effects of the lysophospholipids sphingosine-1-phosphate and lysophosphatidic acid were studied in cultured murine microglia using the patch-clamp and video imaging techniques. Both lysophospholipids induced transient membrane hyperpolarization and K(+) current activation. The lysophospholipid-induced K(+) current was blocked by charybdotoxin or iberiotoxin, but was unaffected by apamin. In recordings with 1 microM intracellular free Ca(2+), Ca(2+)-dependent K(+) currents of microglia showed a similar pharmacological profile to lysophospholipid-induced currents. The Ca(2+)-dependent K(+) channels activated in microglia by lysophospholipids are most likely encoded by the IKCa1 channel gene. The presence of IKCa1 mRNA in microglia was demonstrated by reverse transcriptase-polymerase chain reaction studies. Ca(2+) imaging experiments revealed increases in the intracellular free Ca(2+) concentration of microglia to a mean value of about 400 nM after application of 1 microM sphingosine-1-phosphate or 1 microM lysophosphatidic acid. We suggest that the transient membrane hyperpolarization seen in microglia following exposure to sphingosine-1-phosphate or lysophosphatidic acid is caused by activation of IKCa1 Ca(2+)-dependent K(+) channels. Increases in the concentration of intracellular free Ca(2+) evoked by the lysophospholipids are sufficient to activate microglial Ca(2+)-dependent K(+) channels.
机译:使用膜片钳和视频成像技术在培养的鼠小胶质细胞中研究了溶血磷脂-1-磷酸鞘氨醇和溶血磷脂酸的作用。两种溶血磷脂诱导瞬时膜超极化和K(+)电流激活。溶血磷脂诱导的K(+)电流被charybdotoxin或iberiotoxin所阻止,但不受apamin影响。在具有1 microM胞内游离Ca(2+)的记录中,小胶质细胞的Ca(2+)依赖性K(+)电流显示出与溶血磷脂诱导的电流相似的药理作用。由溶血磷脂在小胶质细胞中激活的Ca(2+)依赖性K(+)通道最有可能由IKCa1通道基因编码。逆转录酶-聚合酶链反应研究证明了IKCa1 mRNA在小胶质细胞中的存在。 Ca(2+)成像实验显示,应用1 microM鞘氨醇-1-磷酸或1 microM溶血磷脂酸后,小胶质细胞内游离Ca(2+)浓度增加到平均值约为400 nM。我们建议在小胶质细胞暴露于鞘氨醇-1-磷酸或溶血磷脂酸后看到的瞬时膜超极化是由IKCa1 Ca(2+)依赖性K(+)通道的激活引起的。溶血磷脂引起的细胞内游离Ca(2+)浓度的增加足以激活小胶质细胞Ca(2+)依赖性K(+)通道。

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