| Literature DB >> 27457803 |
Koichi Inoue1, Eisuke Sakuma2, Hiroyuki Morimoto3, Hayato Asai2, Yoshinori Koide3, Tiandong Leng4, Ikuo Wada3, Zhi-Gang Xiong4, Takatoshi Ueki2.
Abstract
Microglia are derived from myelogenous cells and contribute to immunological and inflammatory responses in central nervous system. They play important roles not only in infectious diseases and inflammation after stroke, but also in psychiatric diseases such as schizophrenia. While recent studies suggest the significances of serum- and glucocorticoid-inducible kinases (SGKs) in other immune cells such as macrophages, T cells and dendritic cells, their role in microglia remains unknown. Here we, for the first time, report that SGK1 and SGK3 are expressed in multiple microglial cell lines. An SGK inhibitor, gsk650394, inhibits cell viability. In addition, lipopolysaccharide-induced expression of inflammatory regulators iNOS and TNFα was enhanced by gsk650394. Furthermore, translocation of NF-κB was enhanced by gsk650394. Taken together, these findings suggest that SGKs may play an important role in regulating microglial viability and inflammatory responses.Entities:
Keywords: Inflammation; Microglia; NF-κB; SGK1; iNOS
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Year: 2016 PMID: 27457803 PMCID: PMC4996278 DOI: 10.1016/j.bbrc.2016.07.094
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575