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新型嘌呤受体诱发大鼠巨核细胞胞质Ca2+振荡

Cytoplasmic Ca2+ oscillation in rat megakaryocytes evoked by a novel type of purinoceptor.

作者信息

Uneyama C, Uneyama H, Akaike N

机构信息

Department of Neurophysiology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Physiol. 1993 Oct;470:731-49. doi: 10.1113/jphysiol.1993.sp019885.

Abstract
  1. The responses of megakaryocytes isolated from rat bone marrow to externally applied adenosine triphosphate (ATP) were investigated in the whole-cell mode by the use of nystatin perforated patch-clamp technique. 2. ATP at 1-100 microM evoked periodic outward currents at a holding potential of -40 mV. The reversal potential of the currents was close to K+ equilibrium potential (EK) and the K+ channel blockers such as quinine and quinidine suppressed the currents, indicating that the outward currents are predominantly carried by K+. 3. Since it has been reported that adenosine diphosphate (ADP) evoked monophasic K+ current using a conventional whole-cell recording, we compared the results obtained by perforated and conventional patch-clamp techniques. The crucial difference between our results and previous results was due to the intracellular perfusion with internal solution containing a high concentration of EGTA by which both current shape and concentration response were modified. 4. The membrane permeable Ca2+ chelator, 1,2-bis(O-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxy methyl ester; BAPTA AM), inhibited the K+ current concentration dependently, suggesting that ATP-induced oscillatory K+ currents are caused by changes in cytoplasmic free Ca2+ concentration ([Ca2+]i). 5. With increasing ATP concentration, the frequency and the maximum amplitude of K+ current oscillation increased and the latency of current, which is the period required to activate the first K+ current after ATP application, decreased. 6. ADP, 2-methylthio-ATP and ATP-gamma-S could also evoke the periodic K+ currents, but adenosine, uridine triphosphate (UTP) and alpha-beta-methylene adenosine 5'-triphosphate (AMP-CPP) failed. 2-Methylthio-ATP was the most potent agonist; next was ADP which showed a 10-30 times stronger effect than ATP. Cross-desensitization was observed between ATP and ADP, but not between ATP or ADP and thrombin. 7. Extracellular Ca2+ was not required for the ATP-induced K+ current activation, indicating that Ca2+ released from intracellular pools induced the oscillatory response. In addition, the agonist potency increased when extracellular Ca2+ concentration ([Ca2+]o) decreased, suggesting that the principal agonists might be ATP4- and ADP3-. 8. The results suggest the presence of a novel subtype of purinoceptor in the megakaryocyte plasma membrane which induces cytoplasmic Ca2+ oscillation and evokes periodic K+ current flux.
摘要
  1. 采用制霉菌素穿孔膜片钳技术,在全细胞模式下研究了从大鼠骨髓分离的巨核细胞对外源性三磷酸腺苷(ATP)的反应。2. 1 - 100微摩尔的ATP在 - 40毫伏的钳制电位下诱发周期性外向电流。电流的反转电位接近钾离子平衡电位(EK),奎宁和奎尼丁等钾离子通道阻滞剂可抑制该电流,表明外向电流主要由钾离子携带。3. 由于已有报道称二磷酸腺苷(ADP)使用传统全细胞记录可诱发单相钾离子电流,我们比较了穿孔膜片钳技术和传统膜片钳技术获得的结果。我们的结果与先前结果的关键差异在于,用含有高浓度乙二醇双(2 - 氨基乙基醚)四乙酸(EGTA)的内部溶液进行细胞内灌注,从而改变了电流形状和浓度反应。4. 膜通透性钙离子螯合剂1,2 - 双(O - 氨基苯氧基)乙烷 - N,N,N',N' - 四乙酸(乙酰氧甲酯;BAPTA AM)浓度依赖性地抑制钾离子电流,表明ATP诱导的振荡性钾离子电流是由细胞质游离钙离子浓度([Ca2 + ]i)的变化引起的。5. 随着ATP浓度增加,钾离子电流振荡的频率和最大幅度增加,电流潜伏期(即施加ATP后激活第一个钾离子电流所需的时间)缩短。6. ADP、2 - 甲硫基ATP和ATP - γ - S也可诱发周期性钾离子电流,但腺苷、三磷酸尿苷(UTP)和α - β - 亚甲基腺苷5'-三磷酸(AMP - CPP)则不能。2 - 甲硫基ATP是最有效的激动剂;其次是ADP,其作用比ATP强10 - 30倍。在ATP和ADP之间观察到交叉脱敏,但在ATP或ADP与凝血酶之间未观察到。7. ATP诱导的钾离子电流激活不需要细胞外钙离子,表明从细胞内钙库释放的钙离子诱导了振荡反应。此外,当细胞外钙离子浓度([Ca2 + ]o)降低时,激动剂效力增加,表明主要激动剂可能是ATP4 - 和ADP3 - 。8. 结果表明,在巨核细胞质膜中存在一种新型嘌呤受体亚型,它可诱导细胞质钙离子振荡并引发周期性钾离子电流通量。

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