2010 Fiscal Year Final Research Report
Intranuclear action of Cell cycle-specific growth inhibitory factor, CDT
Project/Area Number |
20592140
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Morphological basic dentistry
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Research Institution | Hiroshima University |
Principal Investigator |
SUGAI Motoyuki Hiroshima University, 大学院・医歯薬学総合研究科, 教授 (10201568)
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Project Period (FY) |
2008 – 2010
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Keywords | 口腔細菌 / CDT / 細胞死 / 細胞周期 / 歯周病 / Aggregatibactor actinomycetemcomitans |
Research Abstract |
When CdtB was expressed in yeat, Cdt acted as cytolethal and inhibited cell cycle at S/G2. Effect of mutation of DNA repair system on CDT-induced cell death was studied. Mutants of ead51, mre11, rad50 and wrs2 were found to be highly sensitive to CdtB. Further effect of mutation of apoptotic pathway on CDT-induced cell death was studied. Mutants of yca1 and aif1 did not change their susceptibility to CdtB. These resuts suggest that Cdt-induced yeast cell death is not dependent on apoptosis.
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Research Products
(5 results)
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[Journal Article] Cytolethal distending toxin induces caspase-dependent and -independent cell death in MOLT-4 and Jurkat cells.2008
Author(s)
Ohara, M., Hayashi, T., Kusunoki, Y., Nakachi, K., Fujiwara, T., Komatsuzawa, H., Sugai, M.
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Journal Title
Infection and Immunity 76(10)
Pages: 4783-4791
Peer Reviewed
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[Presentation] Cytolethal distending toxin from Aggregatibacter actinomycetemcomitans induces DNA damage, S/G2 cell cycle arrest and caspase-independent death in budding yeast model.2009
Author(s)
Matangkasombut, O., Wattanawaraporn, R., Tsuruda, K., Ohara, M., Sugai, M., Mongkolsuk, S.
Organizer
3^<rd> Hiroshima Conference on Education and Science in Dentistry
Place of Presentation
Hiroshima
Year and Date
20091107-20091108