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논문검색

Basigin/CD147 Promotes the Activation of Signal Transduction Mediated by MyD88 and TRIF

초록

영어

Basigin/EMMPRIN/CD147 has been reported to be associated with inflammatory diseases and cancers. Detailed insight into this multifunctional protein in the context of cellular functions may provide a key to its pathophysiological role in many diseases. Here, we investigated the potential role of basigin in activation of the NF-B and AP-1 signaling cascades associated with the MyD88 and TRIF adaptor proteins. MyD88- and TRIF-dependent activation of NF-B signaling pathway was inhibited by basigin-specific antibody and siRNA. In addition, induction of TRIF-dependent, but MyD88-independent, AP-1 activation was inhibited by basigin-specific siRNA. Taken together, these results suggest that basigin plays a key regulatory role in activation of MyD88- and TRIF-mediated cell signaling pathways, and provide an important insight into basigin-mediated cellular processes that can serve as a guide for the development of new anti-inflammatory therapeutics via intervention in basigin-mediated cellular functions.

목차

Abstract
 1. Introduction
 2. Materials and Methods
  2.1. Flow cytometry
  2.2. Immunoblotting
  2.3. Luciferase reporter assay
  2.4. Small interfering RNA (siRNA)-directed basigin knockdown
 3. Result
  3.1. Effect of basigin on activation of the MyD88-dependent NF-B signaling pathway
  3.2. Effect of basigin on activation of the TRIF-dependent NF-B signaling pathway
  3.3. Effect of basigin on activation of the TRIF-dependent AP-1 signaling pathway
 4. Discussion
 Acknowledgements
 References

저자정보

  • Jieun Jeong Department of Systems Immunology, College of Biomedical Science, Kangwon National University, Chuncheon 200-701, Korea
  • Eunhee G. Kim Department of Systems Immunology, College of Biomedical Science, Kangwon National University, Chuncheon 200-701, Korea
  • Jae Y. Cho Department of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea
  • Eugene C. Yi Department of Molecular Medicine and Biopharmaceutical Sciences, Seoul National University, Seoul, Korea
  • Kristine M. Kim Department of Systems Immunology, College of Biomedical Science, Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon, 200-701, Korea

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