2014 Fiscal Year Final Research Report
Identification of a new type of monocytic cell that promotes affinity maturation and characterization of its B cell-activation mechanism
Project/Area Number |
24560961
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biofunction/Bioprocess
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Research Institution | Okayama University |
Principal Investigator |
OHMORI HITOSHI 岡山大学, 自然科学研究科, 教授 (70116440)
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Co-Investigator(Renkei-kenkyūsha) |
MAGARI Masaki 岡山大学, 大学院自然科学研究科, 助教 (50359882)
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Keywords | 濾胞樹状細胞 / 単球系細胞分化 / CSF-1受容体 / IL-34 / CSF-1 / 細胞情報伝達 / 胚中心B細胞 / マイクロRNA |
Outline of Final Research Achievements |
B cells differentiate into high-afffinity antibody producers as the consequence of hypermutation immunoglobulin genes followed by selection of mutated clones. Follicular dendritic cells (FDCs) have been shown to play a pivotal role in these processes. To investigate immunologic functions of FDCs、we established an FDC line, FL-Y, which was shown to induce a new class of monocytic cells named FDMCs with a unique B cell stimulating activity. We found FDMC differentiation was strictly dependent on CSF-1 receptor (R) and the ligand, IL-34. This is the first report describing IL-34-selective CSF-1R signaling pathway.
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Free Research Field |
細胞工学・免疫学
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