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培养的皮质星形胶质细胞中 A1 和 A2 腺苷受体对 ATP 诱导的钙信号的差异调节

Differential modulation of ATP-induced calcium signalling by A1 and A2 adenosine receptors in cultured cortical astrocytes.

作者信息

Alloisio Susanna, Cugnoli Carlo, Ferroni Stefano, Nobile Mario

机构信息

Institute of Biophysics, CNR, Via De Marini 6, 16149 Genoa, Italy.

出版信息

Br J Pharmacol. 2004 Mar;141(6):935-42. doi: 10.1038/sj.bjp.0705707. Epub 2004 Mar 1.

Abstract
  1. Despite the accumulating evidence that under various pathological conditions the extracellular elevation of adenine-based nucleotides and nucleosides plays a key role in the control of astroglial reactivity, how these signalling molecules interact in the regulation of astrocyte function is still largely elusive. 2. The action of the nucleoside adenosine in the modulation of the intracellular calcium signalling (Ca(2+)) elicited by adenosine 5'-triphosphate (ATP)-induced activation of P2 purinoceptors was investigated on neocortical type-1 astrocytes in primary culture by using single-cell microfluorimetry. 3. Astrocyte challenge with ATP (1-10 microm) elicited biphasic Ca(2+) responses consisting of an initial peak followed by a sustained elevation. The stable adenosine analogue 2-chloroadenosine (2-ClA) potentiated the transient Ca(2+) rise induced by activation of metabotropic P2Y receptors. Among the various P1 receptor agonists tested, the nonselective agonist 5'-N-ethylcarboxamidoadenosine (NECA) mimicked the 2-ClA action, whereas the selective A1 R(-) N6-(2-phenylisopropyl)-adenosine (R-PIA), the A2A 2-[4-(2-carboxyethyl)phenethylamino]-5'-N-ethylcarboxamidoadenosine (CGS-21680) and A3 1-deoxy-1-(6-[([3-lodophenyl]methyl)-amino]-9H-purin-9-yl)-N-methyl-beta-d-ribofuranuronamide (IB-MECA) agonists were ineffective. 4. Application of R-PIA>NECA>or=2-ClA depressed the Ca(2+) plateau reversibly. Moreover, in the presence of R-PIA or 2-ClA, the prolonged Ca(2+) signal was maintained by application of the A1 antagonist 1,3-diethyl-8-phenylxanthine (DPX). Finally, preincubation of the astrocytes with pertussis toxin abrogated the 2-ClA inhibition of the ATP-elicited sustained Ca(2+) rise without affecting the transient Ca(2+) potentiation. 5. Taken together, these findings indicate that stimulation of A1 and A2 adenosine receptors mediates a differential modulation of Ca(2+) signalling elicited by P2 purinoceptors. Since variations in Ca(2+) dynamics also affect cell proliferation and differentiation, our data suggest that tuning of the extracellular levels of adenosine may be relevant for the control of astrogliosis mediated by adenine nucleotides.
摘要
  1. 尽管越来越多的证据表明,在各种病理条件下,细胞外腺嘌呤核苷酸和核苷的升高在星形胶质细胞反应性的控制中起关键作用,但这些信号分子如何在星形胶质细胞功能调节中相互作用仍 largely 难以捉摸。2. 通过单细胞微荧光法,研究了核苷腺苷对原代培养的新皮质 1 型星形胶质细胞中由腺苷 5'-三磷酸(ATP)诱导的 P2 嘌呤受体激活所引发的细胞内钙信号(Ca(2+))的调节作用。3. 用 ATP(1 - 10 微摩尔)刺激星形胶质细胞引发双相Ca(2+)反应,包括一个初始峰值,随后是持续升高。稳定的腺苷类似物 2 - 氯腺苷(2 - ClA)增强了由代谢型 P2Y 受体激活诱导的短暂Ca(2+)升高。在测试的各种 P1 受体激动剂中,非选择性激动剂 5'-N - 乙基羧酰胺腺苷(NECA)模拟了 2 - ClA 的作用,而选择性 A1 R(-) N6-(2 - 苯基异丙基)-腺苷(R - PIA)、A2A 2-[4-(2 - 羧乙基)苯乙氨基]-5'-N - 乙基羧酰胺腺苷(CGS - 21,680)和 A3 1 - 脱氧 - 1-(6 - [([3 - 碘苯基]甲基)-氨基]-9H - 嘌呤 - 9 - 基)-N - 甲基 - β - d - 核糖呋喃酰胺(IB - MECA)激动剂无效。4. 应用 R - PIA > NECA > 或 = 2 - ClA 可逆地抑制Ca(2+)平台期。此外,在存在 R - PIA 或 2 - ClA 的情况下,通过应用 A1 拮抗剂 1,3 - 二乙基 - 8 - 苯基黄嘌呤(DPX)维持延长的Ca(2+)信号。最后,用百日咳毒素预孵育星形胶质细胞消除了 2 - ClA 对 ATP 引发的持续Ca(2+)升高的抑制作用,而不影响短暂的Ca(2+)增强作用。5. 综上所述,这些发现表明,A1 和 A2 腺苷受体的刺激介导了对由 P2 嘌呤受体引发的Ca(2+)信号的差异调节。由于Ca(2+)动力学的变化也影响细胞增殖和分化,我们的数据表明,调节细胞外腺苷水平可能与控制由腺嘌呤核苷酸介导的星形胶质细胞增生有关。

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