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Publication : Increased nucleolar localization of SpiA3G in classically but not alternatively activated macrophages.

First Author  Konjar S Year  2010
Journal  FEBS Lett Volume  584
Issue  11 Pages  2201-6
PubMed ID  20338168 Mgi Jnum  J:172943
Mgi Id  MGI:5009356 Doi  10.1016/j.febslet.2010.03.031
Citation  Konjar S, et al. (2010) Increased nucleolar localization of SpiA3G in classically but not alternatively activated macrophages. FEBS Lett 584(11):2201-6
abstractText  Macrophages play a key role in innate immune response to pathogens and in tissue homeostasis, inflammation and repair. A serpin A3G (SpiA3G) is highly induced in classically activated macrophages. We show increased localization of SpiA3G in the nucleolus and co-localization with cathepsin L, upon classical, but not alternative activation of macrophages. Despite the increased expression of cathepsin L in the nuclei of classically activated macrophages, no cathepsin activity was detected. Since only pro-inflammatory, but not anti-inflammatory stimuli induce increased nucleolar localization of SpiA3G, we propose that SpiA3g translocation into the nucleolus is important in host defense against pathogens.
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