1. MDA5 and ISG56 mediate CXCL10 expression induced by toll-like receptor 4 activation in U373MG human astrocytoma cells.
- Author
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Imaizumi T, Murakami K, Ohta K, Seki H, Matsumiya T, Meng P, Hayakari R, Xing F, Aizawa-Yashiro T, Tatsuta T, Yoshida H, and Kijima H
- Subjects
- Adaptor Proteins, Signal Transducing, Astrocytes immunology, Astrocytes metabolism, Astrocytoma immunology, Cells, Cultured, Humans, Interferon-Induced Helicase, IFIH1, Lipopolysaccharides immunology, NF-kappa B immunology, NF-kappa B metabolism, RNA-Binding Proteins, Signal Transduction, p38 Mitogen-Activated Protein Kinases metabolism, Astrocytoma metabolism, Chemokine CXCL10 metabolism, DEAD-box RNA Helicases metabolism, Toll-Like Receptor 4 metabolism, Transcription Factors metabolism
- Abstract
Toll-like receptor (TLR) 4 is a pattern recognition receptor, and recognizes not only bacterial lipopolysaccharide (LPS) but also endogenous danger-associated molecular patterns released from dying or injured cells. It has been reported that TLR4 signaling in astrocytes plays an important role in various neurological diseases. However, details of TLR4 signaling in astrocytes are not fully elucidated. In the present study, we demonstrated that TLR4 signaling, induced by LPS, increases the expression of melanoma differentiation-associated gene 5 (MDA5) and interferon (IFN)-stimulated gene 56 (ISG56) in U373MG human astrocytoma cells. We also found that nuclear factor-κB, p38 mitogen-activated protein kinase and IFN-β are involved in the expression of MDA5 and ISG56 induced by LPS. RNA interference experiments revealed that MDA5 and ISG56 positively regulate the LPS-induced expression of a chemokine CXCL10, but not CCL2. In addition, it was suggested that MDA5 and ISG56 constitute a positive feedback loop. These results suggest that MDA5 and ISG56 may contribute not only to physiological inflammatory reactions but also to the pathogenesis of various neurological diseases elicited by TLR4 in astrocytes, at least in part, by regulating the expression of CXCL10., (Copyright © 2013 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.)
- Published
- 2013
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