𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stimulation of glucocorticoid-induced tumor necrosis factor receptor family-related protein ligand (GITRL) induces inflammatory activation of microglia in culture

✍ Scribed by Heehong Hwang; Shinrye Lee; Won-Ha Lee; Ho-Jae Lee; Kyoungho Suk


Book ID
102909218
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
526 KB
Volume
88
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Glucocorticoid‐induced tumor necrosis factor receptor family‐related protein ligand (GITRL) is a member of the tumor necrosis factor superfamily (TNFSF) and is known to act as a costimulator in the immune system by binding to GITR. GITRL is expressed in endothelial cells, dendritic cells, macrophages, and B cells, but it is not known whether GITRL is expressed in brain microglia cells. Here, we investigated the expression of GITR and GITRL and their potential role in microglia cells. Using BV‐2 mouse microglia cells and mouse primary microglia cultures, we have demonstrated that 1) both GITR and GITRL are expressed in microglia cells; 2) stimulation of GITRL induces inflammatory activation of microglia on the basis of production of nitric oxide (NO) and expression of inducible nitric oxide synthase, cyclooxygenase‐2, CD40, and matrix metalloproteinase‐9; 3) GITRL‐mediated microglial NO production partially depends on p38 MAPK, JNK, and nuclear factor‐κB pathways; and 4) GITRL stimulation also induces microglia cell death. These results indicate that GITR and GITRL are functionally expressed on brain microglia and that the stimulation of GITRL can induce inflammatory activation of microglia. The GITR/GITRL system may play an important role in neuroinflammation. © 2010 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


p38 Mitogen-activated protein kinase mod
✍ J. Lee; J.-S. Shin; J.Y. Park; D. Kwon; S.-J. Choi; S.-J. Kim; I.-H. Choi 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 239 KB

## Abstract This study describes the involvement of the p38 mitogen‐activated protein kinase (MAPK) during interferon‐γ (IFN‐γ) signaling in fetal brain astrocytes. In some pathological conditions of brain, p38 MAPK transduces stress‐related signals, increases expression of proinflammatory cytokine