Hsp90 controls immune response through spatio-temporal regulation of chaperoned molecule via targeting dendritic cells
| Project/Area Number |
21790359
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Human pathology
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| Research Institution | Sapporo Medical University |
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Principal Investigator |
OKUYA Koichi Sapporo Medical University, 医学部, 研究員 (70457703)
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| Project Period (FY) |
2009 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2009: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | Hsp90 / 樹状細胞 / 初期エンドソーム / 腫瘍免疫 |
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| Research Abstract |
Recent studies have suggested that Toll-like recepor 9 (TLR9) signaling in early endosomes leads to interferon-a production by plasmacytoid dendritic cells (pDCs), whereas TLR9 signaling in late endosomes induces pDC maturation, IL-6 and TNF-a secretion. Here we show that human DNA as well as CpG-oligodeoxynucleotides (ODNs) in complex with heat shock protein 90 (Hsp90) stimulate pDCs to produce large quantities of IFN-a. The Hsp90-CpG-A complexes are targeted into the Rab5^+, EEA1^+- "static" early endosome after internalization by DCs, suggesting that preferential sorting of Hsp90 chaperoned self-DNA/CpG-ODNs to the static endosome is required for signaling through TLR9 for IFN-a production. Thus, extracellular Hsp90 converts inert self-DNA/CpG-ODNs into a potent trigger of IFN-a production via spatiotemporal regulation.
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Report
(3 results)
Research Products
(20 results)
