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在DDT1MF-2细胞中,通过百日咳毒素敏感和不敏感的G蛋白与磷脂酶C偶联的受体之间的细胞内串扰。

Intracellular cross-talk between receptors coupled to phospholipase C via pertussis toxin-sensitive and insensitive G-proteins in DDT1MF-2 cells.

作者信息

Dickenson J M, Hill S J

机构信息

Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham.

出版信息

Br J Pharmacol. 1993 Jul;109(3):719-24. doi: 10.1111/j.1476-5381.1993.tb13633.x.

Abstract
  1. The effect on intracellular free calcium concentration ([Ca2+]i) of simultaneous activation of receptors coupled to phospholipase C via pertussis toxin (PTX)-sensitive and -insensitive G-proteins has been investigated in the hamster vas deferens smooth muscle cell line, DDT1MF-2. 2. In fura-2-loaded DDT1MF-2 cells, activation of adenosine A1-receptors (which are linked to PTX-sensitive G-proteins) with a maximal concentration of N6-cyclopentyladenosine (CPA; 300 nM) increased [Ca2+]i from 121 +/- 5 nM to 254 +/- 20 nM (n = 8). These experiments were performed in the presence of extracellular Ca2+. Stimulation of histamine H1-receptors (which are linked to PTX-insensitive G-proteins) with a low concentration of histamine (1 microM) increased [Ca2+]i from 128 +/- 8 nM to 150 +/- 13 nM (n = 8). When combined, CPA (300 nM) and histamine (1 microM) synergistically raised [Ca2+]i from 134 +/- 6 nM to 607 +/- 61 nM (n = 8). 3. Removal of extracellular Ca2+ (experiments performed in Ca(2+)-free buffer containing 0.1 mM EGTA) had no effect on the synergistic interaction between CPA (300 nM) and histamine (1 microM). 4. The addition of maximal concentrations of CPA (300 nM) and histamine (100 microM) resulted in a rise in [Ca2+]i which was additive when compared to the Ca2+ responses obtained with the two agonists alone. Low (30 nM) and subthreshold (3 nM) concentrations of CPA did not alter the Ca2+ response elicited by maximal concentrations of histamine (100 microM). 5. Subthreshold concentrations of CPA (3 nM) and low concentrations of histamine (1 microM) elicited synergistic rises in [Ca2+]i. 6 Synergistic Ca2+ responses were not observed between histamine Hl- and ATP-receptors when cells were simultaneously stimulated with either 1 microM or 10 microM of each agonist.7 These data suggest that adenosine A1-receptors linked to PTX-sensitive G-protein(s) and histamine H14-receptors linked to PTX-insensitive G-proteins interact synergistically to raise [Ca2+]i. In contrast,activation of ATP-receptors which are linked to PTX-insensitive G-protein(s) do not interact synergically with histamine H1-receptors.
摘要
  1. 我们在仓鼠输精管平滑肌细胞系DDT1MF-2中,研究了通过百日咳毒素(PTX)敏感和不敏感的G蛋白偶联受体同时激活对细胞内游离钙浓度([Ca2+]i)的影响。2. 在装载fura-2的DDT1MF-2细胞中,用最大浓度的N6-环戊基腺苷(CPA;300 nM)激活腺苷A1受体(与PTX敏感的G蛋白相连),使[Ca2+]i从121±5 nM增加到254±20 nM(n = 8)。这些实验是在细胞外存在Ca2+的情况下进行的。用低浓度组胺(1 μM)刺激组胺H1受体(与PTX不敏感的G蛋白相连),使[Ca2+]i从128±8 nM增加到150±13 nM(n = 8)。当CPA(300 nM)和组胺(1 μM)联合使用时,协同使[Ca2+]i从134±6 nM升高到607±61 nM(n = 8)。3. 去除细胞外Ca2+(在含有0.1 mM EGTA的无Ca2+缓冲液中进行实验)对CPA(300 nM)和组胺(1 μM)之间的协同相互作用没有影响。4. 添加最大浓度的CPA(300 nM)和组胺(100 μM)导致[Ca2+]i升高,与单独使用两种激动剂获得的Ca2+反应相比,这种升高是相加的。低浓度(30 nM)和阈下浓度(3 nM)的CPA不会改变最大浓度组胺(100 μM)引起的Ca2+反应。5. 阈下浓度的CPA(3 nM)和低浓度组胺(1 μM)引起[Ca2+]i的协同升高。6. 当用1 μM或10 μM的每种激动剂同时刺激细胞时,组胺H1受体和ATP受体之间未观察到协同的Ca2+反应。7. 这些数据表明,与PTX敏感的G蛋白相连的腺苷A1受体和与PTX不敏感的G蛋白相连的组胺H1受体相互协同作用以升高[Ca2+]i。相比之下,与PTX不敏感的G蛋白相连的ATP受体激活后不会与组胺H1受体发生协同作用。

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