2006 Fiscal Year Final Research Report Summary
Biological function of Ah receptor
| Project/Area Number |
17590112
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Environmental pharmacy
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| Research Institution | Research Institute for Clinical Oncology, Saitama Cancer Center |
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Principal Investigator |
IKUTA Togo Institute for Clinical Oncology, Saitama Cancer Center, Researcher, 臨床腫瘍研究所, 主任研究員 (00262072)
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| Co-Investigator(Kenkyū-buntansha) |
KOIKE Manabu Radiation Effect Mechanisms Research Group, National Institute of Radiological Sciences, Researcher, 生体影響機構, 研究員 (70280740)
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| Project Period (FY) |
2005 – 2006
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| Keywords | skin / keratinocyte / epidermal-mesenchymal transition / wound healing |
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| Research Abstract |
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor which was initially identified as an intracellular mediator of the xenobiotic signaling pathway. We previously showed that AhR localizes predominantly in the cytoplasm under high cell densities of a keratinocytes cell line, HaCaT, but accumulates in the nucleus at low cell densities through modulation of its nuclear export activity. In the current report, we show that the Slug, which is a member of the snail/slug family of zinc finger transcriptional repressors critical for induction of epithelial-mesenchymal transitions (EMT), is activated transcriptionally in accordance with nuclear accumulation of AhR. By reporter assay of the promoter of the Slug gene, gel shift and chromatin immunoprecipitation analyses showed that AhR directly binds to xenobiotic responsive element 5 at-0.7 kb of the gene. AhR-targeted gene silencing by small interfering RNA duplexes led to the abolishment of not only CYP1A1 but also Slug induction by 3-methycholanthrene. The Slug was co-localized to the AhR at the wound margins of HaCaT cells, where apparent nuclear distribution of AhR and Slug was observed. The induced Slug was associated with reduction of an epithelial marker of cytokeratin-18 and with an increase in the mesenchymal marker, fibronectin. Surprisingly, TGF-β1-triggering EMT shows nuclear accumulation of AhR, suggesting that TGF-β-and AhR-directed EMTs share, in part, common molecular mechanisms. Taken together, these findings suggest that AhR participated in Slug induction, which, in turn, regulates cellular physiology including cell adhesion and migration.
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