2013 Fiscal Year Final Research Report
Analysis of the role of transcription factor Nrf2 for arteriosclerosis through chronic inflammatory status
Project/Area Number |
24790305
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Pathological medical chemistry
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Research Institution | Tohoku University |
Principal Investigator |
HARADA Nobuhiko 東北大学, 医学(系)研究科(研究院), 助教 (20431439)
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Project Period (FY) |
2012-04-01 – 2014-03-31
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Keywords | マクロファージ / 慢性炎症 |
Research Abstract |
It has become widely accepted that macrophages exhibit heterogeneity in the atherosclerotic plaques during the progression of atherosclerosis. Plaque-associated macrophages can undergo pro- (M1) and anti-inflammatory (M2) polarization depending on the inflammatory status.To clarify the roles of Nrf2 in atherogenesis, we used an ApoE and Nrf2 double KO mouse model. As a result, we have clarified the role of Nrf2 in the M1 macrophage cells during the development of atherosclerosis in late stage, which indicates that Nrf2 may influence the inflammatory reactions in the plaques. The paper containing these results was accepted for publication in FRBM.
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[Journal Article] Nrf2 in bone marrow derived cells positively contributes to the advanced stage of atherosclerotic plaque formation2012
Author(s)
Nobuhiko Harada, Koichi Ito, Tomonori Hosoya, Junsei Mimura, Atsushi Maruyama, Noriko Noguchi, Ken - ichi Yagami, Naoki Morito, Satoru Takahashi, Jon M. Maher, Masayuki Yamamoto, Ken Itoh
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Journal Title
Free Radical Biology and Medicine
Volume: 53
Pages: 2256-2262
DOI
Peer Reviewed
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