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Gender-dependent expression of murine Irf5 gene: implications for sex bias in autoimmunity Free
Hui Shen1,+, Ravichandran Panchanathan1,+, Priya Rajavelu1, Xin Duan1, Karen A. Gould2, and Divaker Choubey1,3,*
1Department of Environmental Health, University of Cincinnati, 3223 Eden Avenue, P.O. Box 670056, Cincinnati, OH 45267, USA
2Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE 68198-5805, USA
3Cincinnati VA Medical Center, Cincinnati, OH 45220, USA *Correspondence to:Divaker Choubey, Tel: +1-513-558-1014; Fax: +1-513-558-0925; E-mail: divaker.choubey@uc.edu
J Mol Cell Biol, Volume 2, Issue 5, October 2010, 284-290,  https://doi.org/10.1093/jmcb/mjq023
Keyword: lupus susceptibility, gender bias, estrogen, interferon, IRF5
Molecular mechanisms that contribute to sex bias in the development of systemic lupus erythematosus (SLE), an autoimmune disease, remain unknown. We found that the expression levels of interferon regulatory factor 5 (IRF5), a lupus susceptibility factor, depend on gender of mice. We found that steady-state levels of the Irf5 mRNA were relatively higher in splenic cells from certain autoimmune-prone mice (for example, NZB and NZB/W F1) than in non-autoimmune C57BL/6 mice. Additionally, levels of Irf5 mRNA and protein were higher in females than in strain and age-matched males. Accordingly, splenic cells from estrogen receptor-alpha (ERα) knockout, when compared with the wild-type (ERα+/+), female mice expressed relatively lower levels of Irf5 mRNA and the treatment of splenic cells with 17β-estradiol increased the levels. Furthermore, splenic B cells from the female mice had relatively more IRF5 protein in the nucleus than the male mice. Collectively, our observations demonstrate a gender bias in the expression and sub-cellular localization of the murine IRF5.