Desai Bimal N, Leitinger Norbert
Department of Pharmacology, University of Virginia , Charlottesville, VA , USA.
Front Immunol. 2014 Nov 27;5:580. doi: 10.3389/fimmu.2014.00580. eCollection 2014.
In addition to a fundamental role in cellular bioenergetics, the purine nucleotide adenosine triphosphate (ATP) plays a crucial role in the extracellular space as a signaling molecule. ATP and its metabolites serve as ligands for a family of receptors that are collectively referred to as purinergic receptors. These receptors were first described and characterized in the nervous system but it soon became evident that they are expressed ubiquitously. In the immune system, purinergic signals regulate the migration and activation of immune cells and they may also orchestrate the resolution of inflammation (1, 2). The intracellular signal transduction initiated by purinergic receptors is strongly coupled to Ca(2+)-signaling, and co-ordination of these pathways plays a critical role in innate immunity. In this review, we provide an overview of purinergic and Ca(2+)-signaling in the context of macrophage phenotypic polarization and discuss the implications on macrophage function in physiological and pathological conditions.
除了在细胞生物能量学中发挥基本作用外,嘌呤核苷酸三磷酸腺苷(ATP)作为一种信号分子在细胞外空间也起着至关重要的作用。ATP及其代谢产物作为一类受体的配体,这些受体统称为嘌呤能受体。这些受体最初是在神经系统中被描述和表征的,但很快就发现它们在全身广泛表达。在免疫系统中,嘌呤能信号调节免疫细胞的迁移和激活,它们还可能协调炎症的消退(1,2)。嘌呤能受体引发的细胞内信号转导与Ca(2+)信号密切相关,这些信号通路的协调在先天免疫中起着关键作用。在这篇综述中,我们概述了巨噬细胞表型极化背景下的嘌呤能和Ca(2+)信号,并讨论了其在生理和病理条件下对巨噬细胞功能的影响。