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钙调神经磷酸酶是丽蝇唾液腺中肌醇三磷酸/钙离子信号通路负反馈回路的一部分。

Calcineurin is part of a negative feedback loop in the InsP3/Ca²⁺ signalling pathway in blowfly salivary glands.

作者信息

Heindorff Kristoffer, Baumann Otto

机构信息

Institute of Biochemistry and Biology, Department of Animal Physiology, University of Potsdam, Karl-Liebknecht-Str. 24/25, 14476 Potsdam, Germany.

Institute of Biochemistry and Biology, Department of Animal Physiology, University of Potsdam, Karl-Liebknecht-Str. 24/25, 14476 Potsdam, Germany.

出版信息

Cell Calcium. 2014 Sep;56(3):215-24. doi: 10.1016/j.ceca.2014.07.009. Epub 2014 Jul 25.

Abstract

The ubiquitous InsP3/Ca(2+) signalling pathway is modulated by diverse mechanisms, i.e. feedback of Ca(2+) and interactions with other signalling pathways. In the salivary glands of the blowfly Calliphora vicina, the hormone serotonin (5-HT) causes a parallel rise in intracellular [Ca(2+)] and [cAMP] via two types of 5-HT receptors. We have shown recently that cAMP/protein kinase A (PKA) sensitizes InsP3-induced Ca(2+) release. We have now identified the protein phosphatase that counteracts the effect of PKA on 5-HT-induced InsP3/Ca(2+) signalling. We demonstrate that (1) tautomycin and okadaic acid, inhibitors of protein phosphatases PP1 and PP2A, have no effect on 5-HT-induced Ca(2+) signals; (2) cyclosporin A and FK506, inhibitors of Ca(2+)/calmodulin-activated protein phosphatase calcineurin, cause an increase in the frequency of 5-HT-induced Ca(2+) oscillations; (3) the sensitizing effect of cyclosporin A on 5-HT-induced Ca(2+) responses does not involve Ca(2+) entry into the cells; (4) cyclosporin A increases InsP3-dependent Ca(2+) release; (5) inhibition of PKA abolishes the effect of cyclosporin A on the 5-HT-induced Ca(2+) responses, indicating that PKA and calcineurin act antagonistically on the InsP3/Ca(2+) signalling pathway. These findings suggest that calcineurin provides a negative feedback on InsP3/Ca(2+) signalling in blowfly salivary glands, counteracting the effect of PKA and desensitizing the signalling cascade at higher 5-HT concentrations.

摘要

普遍存在的肌醇三磷酸/钙离子(InsP3/Ca(2+))信号通路受多种机制调控,即钙离子的反馈作用以及与其他信号通路的相互作用。在丽蝇(Calliphora vicina)的唾液腺中,激素血清素(5-羟色胺,5-HT)通过两种类型的5-HT受体使细胞内[Ca(2+)]和[cAMP]平行升高。我们最近发现,环磷酸腺苷/蛋白激酶A(cAMP/PKA)使InsP3诱导的Ca(2+)释放敏感化。我们现已确定了一种蛋白磷酸酶,它可抵消PKA对5-HT诱导的InsP3/Ca(2+)信号传导的影响。我们证明:(1)蛋白磷酸酶PP1和PP2A的抑制剂 tautomycin和冈田酸对5-HT诱导的Ca(2+)信号无影响;(2)Ca(2+)/钙调蛋白激活的蛋白磷酸酶钙调神经磷酸酶的抑制剂环孢菌素A和FK506会使5-HT诱导的Ca(2+)振荡频率增加;(3)环孢菌素A对5-HT诱导的Ca(2+)反应的敏感化作用不涉及Ca(2+)进入细胞;(4)环孢菌素A增加InsP3依赖性Ca(2+)释放;(5)抑制PKA可消除环孢菌素A对5-HT诱导的Ca(2+)反应的影响,表明PKA和钙调神经磷酸酶在InsP3/Ca(2+)信号通路上起拮抗作用。这些发现表明,钙调神经磷酸酶对丽蝇唾液腺中的InsP3/Ca(2+)信号传导提供负反馈,抵消PKA的作用,并在较高5-HT浓度下使信号级联脱敏。

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