Activation of human alveolar macrophages via P2 receptors: coupling to intracellular Ca2+ increases and cytokine secretion

D Myrtek, T Muller, V Geyer, N Derr… - The Journal of …, 2008 - journals.aai.org
D Myrtek, T Muller, V Geyer, N Derr, D Ferrari, G Zissel, T Durk, S Sorichter, W Luttmann…
The Journal of Immunology, 2008journals.aai.org
Alveolar macrophages play a crucial role in the pathogenesis of inflammatory airway
diseases. By the generation and release of different inflammatory mediators they contribute
to both recruitment of different leukocytes into the lung and to airway remodeling. A potent
stimulus for the release of inflammatory cytokines is ATP, which mediates its cellular effects
through the interaction with different membrane receptors, belonging to the P2X and P2Y
families. The aim of this study was to characterize the biological properties of purinoceptors …
Abstract
Alveolar macrophages play a crucial role in the pathogenesis of inflammatory airway diseases. By the generation and release of different inflammatory mediators they contribute to both recruitment of different leukocytes into the lung and to airway remodeling. A potent stimulus for the release of inflammatory cytokines is ATP, which mediates its cellular effects through the interaction with different membrane receptors, belonging to the P2X and P2Y families. The aim of this study was to characterize the biological properties of purinoceptors in human alveolar macrophages obtained from bronchoalveolar lavages in the context of inflammatory airway diseases. The present study is the first showing that human alveolar macrophages express mRNA for different P2 subtypes, namely P2X 1, P2X 4, P2X 5, P2X 7, P2Y 1, P2Y 2, P2Y 4, P2Y 6, P2Y 11, P2Y 13, and P2Y 14. We also showed that extracellular ATP induced Ca 2+ transients and increased IL-1β secretion via P2X receptors. Furthermore, extracellular nucleotides inhibited production of IL-12p40 and TNF-α, whereas IL-6 secretion was up-regulated. In summary, our data further support the hypothesis that purinoceptors are involved in the pathogenesis of inflammatory lung diseases.
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