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Phosphocholine-Modified Macromolecules and Canonical Nicotinic Agonists Inhibit ATP-Induced IL-1 beta Release
University of Giessen, Germany.
University of Giessen, Germany.
University of Giessen, Germany.
University of Giessen, Germany; University of Giessen, Germany.
Vise andre og tillknytning
2015 (engelsk)Inngår i: Journal of Immunology, ISSN 0022-1767, E-ISSN 1550-6606, Vol. 195, nr 5, s. 2325-2334Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

IL-1 beta is a potent proinflammatory cytokine of the innate immune system that is involved in host defense against infection. However, increased production of IL-1 beta plays a pathogenic role in various inflammatory diseases, such as rheumatoid arthritis, gout, sepsis, stroke, and transplant rejection. To prevent detrimental collateral damage, IL-1 beta release is tightly controlled and typically requires two consecutive danger signals. LPS from Gram-negative bacteria is a prototypical first signal inducing pro-IL-1 beta synthesis, whereas extracellular ATP is a typical second signal sensed by the ATP receptor P2X7 that triggers activation of the NLRP3-containing inflammasome, proteolytic cleavage of pro-IL-1 beta by caspase-1, and release of mature IL-1 beta. Mechanisms controlling IL-1 beta release, even in the presence of both danger signals, are needed to protect from collateral damage and are of therapeutic interest. In this article, we show that acetylcholine, choline, phosphocholine, phosphocholine-modified LPS from Haemophilus influenzae, and phosphocholine-modified protein efficiently inhibit ATP-mediated IL-1 beta release in human and rat monocytes via nicotinic acetylcholine receptors containing subunits alpha 7, alpha 9, and/or alpha 10. Of note, we identify receptors for phosphocholine-modified macromolecules that are synthesized by microbes and eukaryotic parasites and are well-known modulators of the immune system. Our data suggest that an endogenous anti-inflammatory cholinergic control mechanism effectively controls ATP-mediated release of IL-1 beta and that the same mechanism is used by symbionts and misused by parasites to evade innate immune responses of the host.

sted, utgiver, år, opplag, sider
AMER ASSOC IMMUNOLOGISTS , 2015. Vol. 195, nr 5, s. 2325-2334
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-121432DOI: 10.4049/jimmunol.1400974ISI: 000360014200045PubMedID: 26202987OAI: oai:DiVA.org:liu-121432DiVA, id: diva2:855127
Merknad

Funding Agencies|University Medical Centre Giessen and Marburg; Landes-Offensive zur Entwicklung Wissenschaftlich-Okonomischer Exzellenz of the State of Hesse (Nonneuronal Cholinergic Systems); German Research Foundation [GR 1094/6-1]

Tilgjengelig fra: 2015-09-18 Laget: 2015-09-18 Sist oppdatert: 2017-12-04

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