日本毒性学会学術年会
The 6th International Congress of Asian Society of Toxicology
セッションID: SL2
会議情報

Special Lecture
Cellular adaptive response to environmental toxicants and other noxious stimuli
*Young-Joon SURH
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会議録・要旨集 フリー

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抄録
Living organisms are constantly subjected to diverse types of stress both external and internal sources. While excessive stress leads to necrotic or apoptotic death, moderate amounts of noxious stimuli may render the cells adaptive or tolerant to ongoing or subsequent insults. Such adaptive survival response normally accompanies de novo synthesis of proteins through activation of distinct stress-responsive signaling. One of the key signaling molecules involved in cellular adaptation or tolerance to a wide array of noxious stmuli is nuclear transcription factor erythroid 2p45 (NF-E2)-related factor 2 (Nrf2). Our previous studies have revealed that Nrf2 plays a pivotal role in cellular stress response. Nrf2 is sequestered in the cytoplasm as an inactive complex with the inhibitory protein Keap1. Upon activation, Nrf2 binds to antioxidant responsive element (ARE) or electrophile responsive element (EpRE), leading to the coordinated up-regulation of down-stream target genes that boost cellular antioxidant/cytoprotective potential. Many chemopreventive natural products can induce ARE/EpRE-driven upregulation of antioxidant/phase-2 detoxifying enzymes or other cytoprotective proteins, thereby fortifying cellular defence against oxidative, nitrosative and inflammatory insults. Cysteine thiols present in Keap1 functions as a redox sensor in transcriptional regulation of a distinct set of stress responsive/cytoprotective proteins. Some chemopreventive/chemoprotective natural products can induce ARE/EpRE-driven upregulation of cytoprotective gene expression, thereby fortifying cellular defence against oxidative, nitrosative and inflammatory insults. Supported by the Global Core Research Center (GCRC) grant, National Research Foundation-MEST, Republic of Korea.
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© 2012 日本毒性学会
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