Stress Sensor Mechanism by the Keap1-Nrf2 System
| Project/Area Number |
17K15590
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
General medical chemistry
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| Research Institution | Tohoku University |
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Principal Investigator |
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| Research Collaborator |
YAMAMOTO Masayuki
ISO Tatsuro
MURAMATSU Aki
SAITO Ryota
BAIRD Liam
SUDA Hiromi
MORITA Masanobu
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| Project Period (FY) |
2017-04-01 – 2019-03-31
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| Project Status |
Completed (Fiscal Year 2018)
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| Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2018: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | Keap1 / Nrf2 / 過酸化水素 / 遺伝子 / 発現制御 / ストレス |
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| Outline of Final Research Achievements |
The Keap1-Nrf2 system plays a central role in the oxidative stress response, however the identity of the reactive oxygen species sensor within Keap1 remains poorly understood. Here, we show that a Keap1 mutant lacking eleven cysteine residues retains the ability to target Nrf2 for degradation, but is unable to respond to cysteine-reactive Nrf2 inducers. Of the eleven mutated cysteine residues, we found that four are important for sensing hydrogen peroxide. Our analyses revealed that Keap1 utilizes the cysteine residues redundantly to set up an elaborate fail-safe mechanism in which specific combinations of these four cysteine residues can form a disulfide bond to sense hydrogen peroxide. Importantly, this sensing mechanism is distinct from that used for electrophilic Nrf2 inducers, demonstrating that Keap1 is equipped with multiple cysteine-based sensors to detect various endogenous and exogenous stresses.
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| Academic Significance and Societal Importance of the Research Achievements |
酸化ストレスに対する応答系の破綻は様々な疾患発症と密接に関わっている。このような疾患を未然に防ぐ目的で、細胞は環境ストレスに対して素早い応答で対応し、恒常性を維持している。ストレスセンサーKeap1は転写因子Nrf2の活性を制御し、酸化ストレス防御機構の中心的役割を担う鍵因子である。本研究はKeap1が酸化ストレスを感知してNrf2を制御する分子メカニズムの一端を明らかにした。
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Report
(3 results)
Research Products
(22 results)
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[Journal Article] Infiltration of M1, but not M2, macrophages is impaired after unilateral ureter obstruction in Nrf2-deficient mice.2017
Author(s)
Sogawa Y, Nagasu H, Iwae S, Ihoriya C, Itano S, Uchida A, Kidokoro K, Taniguchi S, Takahashi M, Satoh M, Sasaki T, Suzuki T, Yamamoto M, Horng T and Kashihara N.
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Journal Title
Scientific Reports
Volume: 7
Issue: 1
Pages: 8801-8801
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] The novel Nrf2 inducer TFM-735 ameliorates experimental autoimmune encephalomyelitis in mice.2017
Author(s)
Higashi C, Kawaji A, Tsuda N, Hayashi M, Saito R, Yagishita Y, Suzuki T, Uruno A, Nakamura M, Nakao K, Furusako S, Yamamoto M.
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Journal Title
Eur J Pharmacol
Volume: 802
Pages: 76-84
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] The aryl hydrocarbon receptor AhR links atopic dermatitis and air pollution via induction of the neurotrophic factor artemin.2017
Author(s)
Hidaka, T., Ogawa, E., Kobayashi, E.H., Suzuki, T., Funayama, R., Nagashima, T., Fujimura, T., Aiba, S., Nakayama, K., Okuyama, R., Yamamoto, M.
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Journal Title
Nat. Immunol.
Volume: 18
Issue: 1
Pages: 64-73
DOI
Related Report
Peer Reviewed
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