Abstract |
Microglia participate in innate inflammatory responses within the central nervous system. The highly conserved microRNA-9 (miR-9) plays critical roles in neurogenesis as well as axonal extension. Its role in microglial inflammatory responses, however, remains poorly understood. Here we identify a unique role of miR-9 in mediating the microglial inflammatory response via distinct signalling pathways. MiR-9-mediated regulation of cellular activation involved downregulated expression of the target protein, monocyte chemotactic protein-induced protein 1 (MCPIP1) that is crucial for controlling inflammation. Results indicate that miR-9-mediated cellular activation involved signalling via the NF-κB pathway, but not the β- catenin pathway.
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Authors | Honghong Yao, Rong Ma, Lu Yang, Guoku Hu, Xufeng Chen, Ming Duan, Yeonhee Kook, Fang Niu, Ke Liao, Minggui Fu, Gang Hu, Pappachan Kolattukudy, Shilpa Buch |
Journal | Nature communications
(Nat Commun)
Vol. 5
Pg. 4386
(Jul 14 2014)
ISSN: 2041-1723 [Electronic] England |
PMID | 25019481
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- MIRN9 microRNA, mouse
- MIRN9 microRNA, rat
- MicroRNAs
- NF-kappa B
- beta Catenin
- Ribonucleases
- Zc3h12a protein, mouse
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Topics |
- Animals
- Blotting, Northern
- Blotting, Western
- Flow Cytometry
- In Situ Hybridization
- Male
- Mice
- Mice, Inbred C57BL
- MicroRNAs
(genetics, metabolism)
- Microglia
(metabolism)
- NF-kappa B
(genetics, metabolism)
- Rats
- Rats, Sprague-Dawley
- Real-Time Polymerase Chain Reaction
- Ribonucleases
(genetics, metabolism)
- Signal Transduction
(physiology)
- beta Catenin
(genetics, metabolism)
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