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大鼠腹膜肥大细胞中Na+/H(+)交换的双重调节:蛋白激酶C和钙在细胞内pH调节及组胺释放中的作用

Dual regulation of the Na+/H(+)-exchange in rat peritoneal mast cells: role of protein kinase C and calcium on pHi regulation and histamine release.

作者信息

Friis U G, Johansen T

机构信息

Department of Pharmacology, Odense University, Denmark.

出版信息

Br J Pharmacol. 1996 Jul;118(6):1327-34. doi: 10.1111/j.1476-5381.1996.tb15541.x.

Abstract
  1. The purpose of this study was to compare the actions of phorbol 12-myristate 13-acetate (PMA) and ionomycin on Na+/H+ exchange activation and histamine release to that of compound 48/80 in order to study the possible relationship between pHi and secretion of histamine in rat peritoneal mast cells. 2. Resting pHi in mast cells suspended in a bicarbonate-free physiological salt solution amounted to 6.73 +/- 0.05 (mean +/- s.d., n = 52). 3. PMA (20 nM) induced a substantial but rather slow increase in pHi. This response was very sensitive to inhibition by staurosporine, very sensitive to inhibition by 5-(N,N-hexamethylene)amiloride (HMA), insensitive to the absence of extracellular calcium (without EGTA), and sensitive to partial depletion of intracellular calcium with EGTA. 4. Ionomycin (1 microM) induced a biphasic change in pHi that was sensitive to inhibition by HMA, insensitive to staurosporine. In the absence of extracellular calcium using EGTA, the biphasic response disappeared, leaving only a slow, and diminished change in pHi. 5. The effects of ionomycin and PMA on pHi were additive. 6. Addition of the secretagogue compound 48/80 (1 microgram ml-1) increased pHi, substantially, delta pHi amounting to 0.29 +/- 0.05 pH-units (n = 4). The biphasic pHi-response was insensitive to the absence of extracellular calcium (without EGTA). The initial fast response in pHi was, however, inhibited by HMA, not staurosporine. 7. The finding that staurosporine and HMA each inhibited approximately half of the compound 48/80-induced pHi-response, whereas both inhibitors completely abolished the compound 48/80-induced pHi-response seems to indicate that two independent pathways for the activation of the Na+/H+ exchange were stimulated by compound 48/80. 8. The histamine release induced via both PKC activation (using PMA) and calcium (using ionomycin) were much larger than the sum of each activation pathway, whereas in the absence of extracellular calcium using EGTA, the histamine release in response to PMA and ionomycin was completely abolished. 9. The compound 48/80-induced histamine release was partially sensitive to inhibition by HMA (approximately 30% inhibition) and partially sensitive to inhibition by staurosporine (approximately 50% inhibition). Preincubation with staurosporine and HMA before stimulation with compound 48/80 showed the same degree of inhibition as observed after staurosporine alone, even though this combination of drugs completely inhibited the pHi-response. Furthermore, compound 48/80-induced histamine release was not dependent on the presence of extracellular calcium (with and without EGTA). 10. In spite of the similarities in second messenger pathways for pHi regulation and histamine release, it is, however, not very likely that these two processes are directly related. It is, however, possible, that an increase in pHi plays a permissive, rather than an essential role for histamine release in rat peritoneal mast cells. This hypothesis was supported by the finding that preincubation with the Na+/H+ exchange-inhibitor HMA inhibited 30% of the compound 48/80-induced histamine secretion.
摘要
  1. 本研究的目的是比较佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)和离子霉素对Na⁺/H⁺交换激活及组胺释放的作用与化合物48/80的作用,以研究大鼠腹膜肥大细胞中细胞内pH值(pHi)与组胺分泌之间的可能关系。2. 悬浮于无碳酸氢盐生理盐溶液中的肥大细胞静息pHi为6.73±0.05(平均值±标准差,n = 52)。3. PMA(20 nM)引起pHi显著但相当缓慢的升高。该反应对星形孢菌素的抑制非常敏感,对5 -(N,N - 六亚甲基)氨氯吡咪(HMA)的抑制非常敏感,对细胞外钙缺失(无EGTA)不敏感,对用EGTA部分耗尽细胞内钙敏感。4. 离子霉素(1 μM)引起pHi的双相变化,对HMA的抑制敏感,对星形孢菌素不敏感。在使用EGTA使细胞外钙缺失的情况下,双相反应消失,仅留下pHi缓慢且减弱的变化。5. 离子霉素和PMA对pHi的作用是相加的。6. 添加促分泌剂化合物48/80(1 μg/ml)使pHi显著升高,ΔpHi达0.29±0.05 pH单位(n = 4)。双相pHi反应对细胞外钙缺失(无EGTA)不敏感。然而,pHi的初始快速反应受HMA抑制,不受星形孢菌素抑制。7. 星形孢菌素和HMA各自抑制化合物48/80诱导的pHi反应的约一半,而两种抑制剂均完全消除化合物48/80诱导的pHi反应,这一发现似乎表明化合物48/80刺激了两条独立的Na⁺/H⁺交换激活途径。8. 通过蛋白激酶C激活(使用PMA)和钙(使用离子霉素)诱导的组胺释放远大于各激活途径释放之和,而在使用EGTA使细胞外钙缺失的情况下,对PMA和离子霉素的组胺释放完全被消除。9. 化合物48/80诱导的组胺释放对HMA抑制部分敏感(约30%抑制),对星形孢菌素抑制部分敏感(约50%抑制)。在用化合物48/80刺激前用星形孢菌素和HMA预孵育显示出与单独使用星形孢菌素后观察到的相同程度的抑制,尽管这种药物组合完全抑制了pHi反应。此外,化合物48/80诱导的组胺释放不依赖于细胞外钙的存在(有和无EGTA)。10. 尽管在pHi调节和组胺释放的第二信使途径方面存在相似性,但这两个过程不太可能直接相关。然而,pHi升高在大鼠腹膜肥大细胞组胺释放中可能起允许作用而非关键作用。这一假设得到以下发现的支持:用Na⁺/H⁺交换抑制剂HMA预孵育可抑制30%的化合物48/80诱导的组胺分泌。

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