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豚鼠巨核细胞可通过激活钙依赖性钾电导对外部二磷酸腺苷作出反应。

Guinea-pig megakaryocytes can respond to external ADP by activating Ca2(+)-dependent potassium conductance.

作者信息

Kawa K

机构信息

Department of Pharmacology, Gunma University School of Medicine, Maebashi, Japan.

出版信息

J Physiol. 1990 Dec;431:207-24. doi: 10.1113/jphysiol.1990.sp018327.

Abstract
  1. The responses of megakaryocytes to adenosine diphosphate (ADP) were studied using whole-cell patch electrodes and a Ca2(+)-sensitive fluorescent dye, Fura-2. Megakaryocytes (diameter, 17-42 microns) were mechanically dissociated from the bone marrow of adult guinea-pigs and ADP (1-10 microM) was pressure-applied to megakaryocytes under recording. 2. In megakaryocytes immersed in standard saline, ADP evoked an obvious outward current at a membrane potential of -63 mV. The current was identified as a K(+)-carried current, since the reversal potential depended distinctly on the external K+ concentration, but it showed no changes after removal of external Na+. The amplitude of evoked K+ currents showed considerable intercell variation, which is presumably due to differences of current density in the membrane. 3. During application of ADP, the evoked K+ current was not sustained but slowly decayed to become negligible within 10-20 s, suggesting the appearance of desensitization. The response of the megakaryocyte to ADP recovered slowly and returned to an original level after 4-5 min of continuous washing. 4. When the intracellular free Ca2+ concentration ([Ca2+]i) was measured using the Ca2(+)-sensitive fluorescent dye, Fura-2, application of 10 microM-ADP induced an increase of [Ca2+]i by about 5-fold, which was followed by a gradual decay to the original level within 30-50 s. Roles of internal Ca2+ for activating the K+ current were confirmed by observing (1) enhancement of evoked currents by the use of internal saline containing no Ca2+ chelators and (2) generation of prolonged K+ current by application of a Ca2+ ionophore, A23187, to the megakaryocyte. 5. In a fraction of the megakaryocytes, spontaneous hyperpolarization of the resting membrane potential was observed. The hyperpolarization seemed to result from the activation of K+ channels in the membrane, which was caused by spontaneous release of Ca2+ from the internal storage site. 6. It was concluded that megakaryocytes of the guinea-pig can respond to external ADP by increasing [Ca2+]i and consequently by activating Ca2(+)-dependent K+ channels in the membrane.
摘要
  1. 使用全细胞膜片电极和Ca2(+)敏感荧光染料Fura-2研究了巨核细胞对二磷酸腺苷(ADP)的反应。从成年豚鼠骨髓中机械分离出巨核细胞(直径17 - 42微米),并在记录过程中向巨核细胞施加压力注入ADP(1 - 10微摩尔)。2. 在浸于标准盐溶液中的巨核细胞中,ADP在膜电位为 - 63毫伏时诱发明显的外向电流。该电流被确定为K(+)携带电流,因为其反转电位明显取决于外部K+浓度,但去除外部Na+后无变化。诱发的K+电流幅度在细胞间有相当大的差异,这可能是由于膜电流密度不同所致。3. 在施加ADP期间,诱发的K+电流并非持续存在,而是在10 - 20秒内缓慢衰减至可忽略不计,提示出现脱敏现象。巨核细胞对ADP的反应恢复缓慢,持续冲洗4 - 5分钟后恢复到原始水平。4. 当使用Ca2(+)敏感荧光染料Fura-2测量细胞内游离Ca2+浓度([Ca2+]i)时,施加10微摩尔 - ADP会使[Ca2+]i增加约5倍,随后在30 - 50秒内逐渐衰减至原始水平。通过观察(1)使用不含Ca2+螯合剂的内部盐溶液增强诱发电流以及(2)向巨核细胞施加Ca2+离子载体A23187产生延长的K+电流,证实了内部Ca2+在激活K+电流中的作用。5. 在一部分巨核细胞中,观察到静息膜电位的自发性超极化。这种超极化似乎是由膜中K+通道的激活引起的,而这是由内部储存部位的Ca2+自发释放所导致的。6. 得出结论,豚鼠巨核细胞可通过增加[Ca2+]i并因此激活膜中Ca2(+)依赖性K+通道来响应外部ADP。

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