| Literature DB >> 27942582 |
Naoki Nakagawa1,2,3, Luke Barron4, Ivan G Gomez1,2,4, Bryce G Johnson1,2,4, Allie M Roach1,2,4, Sei Kameoka4, Richard M Jack5, Mark L Lupher5, Sina A Gharib2,6,7, Jeremy S Duffield1,2,4.
Abstract
Pentraxin-2 (PTX-2), also known as serum amyloid P component (SAP/APCS), is a constitutive, antiinflammatory, innate immune plasma protein whose circulating level is decreased in chronic human fibrotic diseases. Here we show that recombinant human PTX-2 (rhPTX-2) retards progression of chronic kidney disease in Col4a3 mutant mice with Alport syndrome, reducing blood markers of kidney failure, enhancing lifespan by 20%, and improving histological signs of disease. Exogenously delivered rhPTX-2 was detected in macrophages but also in tubular epithelial cells, where it counteracted macrophage activation and was cytoprotective for the epithelium. Computational analysis of genes regulated by rhPTX-2 identified the transcriptional regulator c-Jun along with its activator protein-1 (AP-1) binding partners as a central target for the function of rhPTX-2. Accordingly, PTX-2 attenuates c-Jun and AP-1 activity, and reduces expression of AP-1-dependent inflammatory genes in both monocytes and epithelium. Our studies therefore identify rhPTX-2 as a potential therapy for chronic fibrotic disease of the kidney and an important inhibitor of pathological c-Jun signaling in this setting.Entities:
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Year: 2016 PMID: 27942582 PMCID: PMC5135274 DOI: 10.1172/jci.insight.87446
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708