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Multiple G-protein-coupling specificity of β-adrenoceptor in macrophages

机译:β-肾上腺素受体在巨噬细胞中的多种G蛋白偶联特异性

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摘要

Adrenergic signalling of the immune system is one of the important modulator pathways of the inflammatory immune response realized via G protein-mediated pathways. The resulted signal depends on the type of the receptor-coupled G-protein (GPCR) that, according to the classical paradigm in the case of β-adrenergic receptor (β-AR), is Gs-type. Recently, alternate and/or multiple G protein coupling specificity of GPCRs have been demonstrated including a switch from Gs to Gi binding. The possibility of a Gs/Gi switch and its role in the immune response of macrophages has not been investigated yet. In this study, we demonstrate that β-adrenergic stimulation itself is able to induce a transient mitogen-activated protein kinase phosphorylation in murine peritoneal macrophages in a pertussis toxin-sensitive manner, suggesting that the Gs/Gi switch also occurs in the immune system. Although this process is very rapid, it can influence different signalling pathways and can reprogramme effector functions suggesting that sympathetic modulation of the defence mechanism of the innate immune system has an additional, Gs/Gi switch-dependent component.
机译:免疫系统的肾上腺素信号传导是通过G蛋白介导的途径实现的炎性免疫反应的重要调节剂途径之一。产生的信号取决于受体偶联的G蛋白(GPCR)的类型,根据经典范例,在β肾上腺素能受体(β-AR)的情况下,该蛋白是Gs型。近来,已经证明了GPCR的交替和/或多种G蛋白偶联特异性,包括从Gs到Gi结合的转变。 Gs / Gi开关的可能性及其在巨噬细胞免疫应答中的作用尚未进行研究。在这项研究中,我们证明β-肾上腺素能刺激本身能够以百日咳毒素敏感的方式在鼠腹膜巨噬细胞中诱导瞬时的促分裂原活化的蛋白激酶磷酸化,表明Gs / Gi开关也发生在免疫系统中。尽管此过程非常迅速,但它可以影响不同的信号传导途径,并且可以重编程效应子功能,这提示先天免疫系统防御机制的交感神经调节具有额外的Gs / Gi开关依赖性成分。

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