@article{open1769,
          volume = {290},
          number = {30},
           month = {July},
          author = {Sahil Mahajan and Ankita Saini and Vemika Chandra and Ravikanth Nanduri and Rashi Kalra and Ella Bhagyaraj and Neeraj Khatri and Pawan Gupta},
            note = {Copyright of this article belongs to ASBMB.},
           title = {Nuclear Receptor Nr4a2 Promotes Alternative Polarization of Macrophages and Confers Protection in Sepsis.},
       publisher = {ASBMB},
            year = {2015},
         journal = {The Journal of biological chemistry},
           pages = {18304--14},
        keywords = {gene transcription; inflammation;macrophage ;
nuclear receptor
sepsis
Arginase 1;},
             url = {http://crdd.osdd.net/open/1769/},
        abstract = {The orphan nuclear receptor Nr4a2 is known to modulate both inflammatory and metabolic processes, but the mechanism by which it regulates innate inflammatory homeostasis has not been adequately addressed. This study shows that exposure to ligands for Toll-like receptors (TLRs) robustly induces Nr4a2 and that this induction is tightly regulated by the PI3K-Akt signaling axis. Interestingly, exogenous expression of Nr4a2 in macrophages leads to their alternative phenotype with induction of genes that are prototypical M2 markers. Moreover, Nr4a2 transcriptionally activates arginase 1 expression by directly binding to its promoter. Adoptive transfer experiments revealed that increased survival of animals in endotoxin-induced sepsis is Nr4a2-dependent. Thus our data identify a previously unknown role for Nr4a2 in the regulation of macrophage polarization.}
}