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P2-嘌呤受体的激活触发了哺乳动物少突胶质细胞中肌醇三磷酸(InsP3)敏感的内部储存库释放钙离子(Ca2+)。

Activation of P2-purinoreceptors triggered Ca2+ release from InsP3-sensitive internal stores in mammalian oligodendrocytes.

作者信息

Kirischuk S, Scherer J, Kettenmann H, Verkhratsky A

机构信息

Max-Delbrück Center for Molecular Medicine, Berlin-Buch, Germany.

出版信息

J Physiol. 1995 Feb 15;483 ( Pt 1)(Pt 1):41-57. doi: 10.1113/jphysiol.1995.sp020566.

Abstract
  1. The subcellular characteristics of an ATP-induced elevation of the cytoplasmic free calcium concentration ([Ca2+]i) were studied in cultured cells of the oligodendrocyte lineage obtained from mouse cortex and rabbit retina, as well as in oligodendrocytes from mouse corpus callosum slices, using laser scanning confocal microfluorometry. 2. With the stage- and lineage-specific antibodies O4 and O10, three developmental stages within the oligodendrocyte lineage were distinguished prior to Ca2+ recording. 3. Bath application of 1-100 microM ATP induced a transient increase of [Ca2+]i in late precursors and oligodendrocytes but not in early glial precursor cells from retinal and cortical cultures and from corpus callosum slices. This effect of ATP was observed in Ca(2+)-free extracellular solution, suggesting that the ATP-mediated elevation of [Ca2+]i is due to a Ca2+ liberation from intracellular stores. 4. In both late precursors and oligodendrocytes from retina, the amplitude of ATP-induced [Ca2+]i transients was significantly higher in processes as compared with the soma; in cortical cultures such an uneven response was only observed in oligodendrocytes, while in immature cells responses in soma and processes were of similar amplitude. 5. The rank order of potency for the purine and pyrimidine nucleotides was UTP > or = ATP > ADP >> AMP = adenosine = Me-ATP for retinal oligodendrocytes, and ADP > or = ATP >> UTP = AMP = adenosine = Me-ATP for cortical oligodendrocytes. The response to ATP and related nucleotides was blocked by suramin, indicating the involvement of a P2-purinoreceptor in the ATP-mediated [Ca2+]i response. 6. ATP-induced elevation of the cytosolic Ca2+ concentration was inhibited by incubating cells with thapsigargin (10 microM) and by intracellular administration of heparin (1 microM). These findings indicate that ATP triggers a release of Ca2+ ions from InsP3-sensitive internal stores. 7. The ATP receptors may play a role in neuron-glial signal transfer; ATP is released as neurotransmitter, but also under pathological conditions from damaged cells.
摘要
  1. 利用激光扫描共聚焦显微荧光测定法,对从小鼠皮质和兔视网膜获取的少突胶质细胞系培养细胞以及小鼠胼胝体切片中的少突胶质细胞进行研究,以探讨ATP诱导的细胞质游离钙浓度([Ca2+]i)升高的亚细胞特征。2. 使用阶段和谱系特异性抗体O4和O10,在记录Ca2+之前区分少突胶质细胞系中的三个发育阶段。3. 浴加1 - 100微摩尔ATP可诱导晚期前体细胞和少突胶质细胞中[Ca2+]i短暂升高,但视网膜和皮质培养物以及胼胝体切片中的早期神经胶质前体细胞中则无此现象。在无钙细胞外溶液中也观察到ATP的这种作用,这表明ATP介导的[Ca2+]i升高是由于细胞内储存库释放Ca2+所致。4. 在视网膜的晚期前体细胞和少突胶质细胞中,与胞体相比,ATP诱导的[Ca2+]i瞬变幅度在突起中显著更高;在皮质培养物中,这种不均匀反应仅在少突胶质细胞中观察到,而在未成熟细胞中,胞体和突起中的反应幅度相似。5. 对于视网膜少突胶质细胞,嘌呤和嘧啶核苷酸的效力顺序为UTP≥ATP>ADP>>AMP = 腺苷 = Me - ATP,而对于皮质少突胶质细胞,效力顺序为ADP≥ATP>>UTP = AMP = 腺苷 = Me - ATP。对ATP及相关核苷酸的反应被苏拉明阻断,表明P2嘌呤受体参与了ATP介导的[Ca2+]i反应。6. 用毒胡萝卜素(10微摩尔)孵育细胞以及细胞内注射肝素(1微摩尔)可抑制ATP诱导的胞质Ca2+浓度升高。这些发现表明ATP触发了从肌醇三磷酸敏感的内部储存库释放Ca2+离子。7. ATP受体可能在神经元 - 神经胶质信号传递中起作用;ATP作为神经递质释放,但在病理条件下也可从受损细胞释放。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/834e/1157870/be36288d147f/jphysiol00325-0046-a.jpg

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