Serum autoantibodies in pristane induced lupus are regulated by neutrophil gelatinase associated lipocalin

Copyright © 2014 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 154(2014), 1 vom: 15. Sept., Seite 49-65
1. Verfasser: Pawar, Rahul D (VerfasserIn)
Weitere Verfasser: Goilav, Beatrice, Xia, Yumin, Zhuang, Haoyang, Herlitz, Leal, Reeves, Westley H, Putterman, Chaim
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Autoantibodies Lipocalin-2 NGAL Pristane SLE Acute-Phase Proteins LCN2 protein, human mehr... Lipocalins Proto-Oncogene Proteins Terpenes Interleukin-12 187348-17-0 pristane 26HZV48DT1
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245 1 0 |a Serum autoantibodies in pristane induced lupus are regulated by neutrophil gelatinase associated lipocalin 
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520 |a The onset of autoantibodies in systemic autoimmunity can be the result of a breakdown in tolerance at multiple checkpoints. Genetic, hormonal, and immunological factors can combine with environmental influences to accelerate the onset of disease and aggravate disease outcome. Here, we describe a novel mechanism relating to the regulatory role of Neutrophil Gelatinase Associated Lipocalin (NGAL) in modulating the levels of autoantibodies in pristane induced lupus. Following a single injection of pristane intraperitoneally, NGAL expression was induced in both the serum and spleen. Furthermore, NGAL deficient mice were more susceptible to the induction of pristane stimulated autoimmunity, and displayed higher numbers of autoantibody secreting cells and increased expression of activation induced cytidine deaminase (AID) and other inflammatory mediators in the spleen. In contrast, kidney damage was milder in NGAL deficient mice, indicating that NGAL was detrimental in autoantibody mediated kidney disease. These studies indicate that NGAL plays differential roles in different tissues in the context of lupus, and suggest a previously unrecognized role for NGAL in adaptive immunity 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Autoantibodies 
650 4 |a Lipocalin-2 
650 4 |a NGAL 
650 4 |a Pristane 
650 4 |a SLE 
650 7 |a Acute-Phase Proteins  |2 NLM 
650 7 |a Autoantibodies  |2 NLM 
650 7 |a LCN2 protein, human  |2 NLM 
650 7 |a Lipocalin-2  |2 NLM 
650 7 |a Lipocalins  |2 NLM 
650 7 |a Proto-Oncogene Proteins  |2 NLM 
650 7 |a Terpenes  |2 NLM 
650 7 |a Interleukin-12  |2 NLM 
650 7 |a 187348-17-0  |2 NLM 
650 7 |a pristane  |2 NLM 
650 7 |a 26HZV48DT1  |2 NLM 
700 1 |a Goilav, Beatrice  |e verfasserin  |4 aut 
700 1 |a Xia, Yumin  |e verfasserin  |4 aut 
700 1 |a Zhuang, Haoyang  |e verfasserin  |4 aut 
700 1 |a Herlitz, Leal  |e verfasserin  |4 aut 
700 1 |a Reeves, Westley H  |e verfasserin  |4 aut 
700 1 |a Putterman, Chaim  |e verfasserin  |4 aut 
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773 1 8 |g volume:154  |g year:2014  |g number:1  |g day:15  |g month:09  |g pages:49-65 
856 4 0 |u http://dx.doi.org/10.1016/j.clim.2014.06.007  |3 Volltext 
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