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Slc11a1 (Nramp-1) gene modulates immune-inflammation genes in macrophages during pristane-induced arthritis in mice.

Authors:
Mara A Correa Tatiane Canhamero Andrea Borrego Iana S S Katz José R Jensen José Luiz Guerra Wafa H K Cabrera Nancy Starobinas Jussara G Fernandes Orlando G Ribeiro Olga M Ibañez Marcelo De Franco

Inflamm Res 2017 Nov 1;66(11):969-980. Epub 2017 Jul 1.

Laboratório de Imunogenética, Instituto Butantan, Avenida Vital Brasil 1500, São Paulo, SP, 05503000, Brazil.

Objective And Design: Pristane-induced arthritis (PIA) in AIRmax mice homozygous for Slc11a1 R and S alleles was used to characterize the influence of Slc11a1 gene polymorphism on immune responses during disease manifestation. Previous reports demonstrated that the presence of the Slc11a1 S allele increased the incidence and severity of PIA in AIRmax , suggesting that this gene could interact with inflammatory loci to modulate PIA. We investigated the effects of Slc11a1 alleles on the activation of phagocytes during PIA.

Treatment: Mice were injected intraperitoneally with two doses of 0.5 mL of mineral oil pristane at 60-day intervals. Arthritis development was accompanied for 180 days.

Results: AIRmax mice showed differential peritoneal macrophage gene expression profiles during PIA, with higher expression and production of HO, NO, IL-1β, IL-6, TNF-α, and several chemokines. The presence of the Slc11a1 R allele, on the other hand, diminished the intensity of macrophage activation, restricting arthritis development.

Conclusion: Our data demonstrated the fine-tuning roles of Slc11a1 alleles modulating macrophage activation, and consequent PIA susceptibility, in those mouse lines.

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http://dx.doi.org/10.1007/s00011-017-1077-8DOI Listing
November 2017

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