Profile Information
- Affiliation
- Faculty of Applied Life Science School of Animal Science, Nippon Veterinary and Life Science University
- J-GLOBAL ID
- 201501004715879753
- researchmap Member ID
- B000250402
Research Interests
27Research Areas
4Research History
6-
Oct, 2004 - May, 2007
Education
2-
1991 - 1995
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1985 - 1991
Papers
44-
J Virol Methods., 311 114644, Jan, 2023 Peer-reviewed
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Journal of Leukocyte Biology, 110(5) 867-884, Nov, 2021 Peer-reviewed
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Immunological investigations, 1-19, Dec 13, 2019 Peer-reviewedBackground: Psychological stress affects the immune system. Upon stress occurrence, glucocorticoid is released that binds to the glucocorticoid receptor and regulates gene expression. Thus, we aimed to examine the stress-induced immunomodulatory mechanisms by investigating the expression patterns of stress-inducible genes in murine immune cells.Methods: BALB/c, C57BL/6, glucocorticoid-receptor congenic mice, and corticotropin-releasing hormone (CRH)-deficient mice were exposed to synthetic glucocorticoid, dexamethasone, or placed under a restraint condition. The expression level of stress-related genes, such as Rtp801, Gilz, Mkp-1, Bnip3, and Trp53inp1 was measured in the immune cells in these mice.Results: Short restraint stress induced Rtp801 and Gilz expressions that were higher in the spleen of BALB/c mice than those in C57BL/6 mice. Mkp-1 expression increased equally in these two strains, despite the difference in the glucocorticoid level. These three genes induced by short restraint stress were not induced in the CRH-deficient mice. In contrast, Bnip3 and Trp53inp1 were only upregulated upon longer restraint events. In the thymus, Trp53inp1 expression was induced upon short restraint stress, whereas Gilz expression constantly increased upon short and repetitive restraint stresses.Conclusion: These results suggest that singular and repetitive bouts of stress lead to differential gene expression in mice and stress-induced gene expression in thymocytes is distinct from that observed in splenocytes. Gilz, Rtp801, and Mkp-1 genes induced by short restraint stress are dependent on CRH in the spleen.
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Immunological investigations, 48(3) 303-320, Apr, 2019 Peer-reviewed
Misc.
32-
日本分子生物学会年会プログラム・要旨集(Web), 41st ROMBUNNO.2P‐0550 (WEB ONLY), 2018
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FASEB JOURNAL, 29, Apr, 2015
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JOURNAL OF MEDICINAL CHEMISTRY, 52(24) 8058-8058, Dec, 2009
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東京女子医科大学総合研究所紀要, 24 26-27, Jul, 2004スーパー抗原によるT細胞の活性化機序と感染症発症機序,さらにヒトとマウスT細胞の分化成熟について解析した.TSST-1やSPE-AはヒトやマウスのMHCクラスII分子に結合しT細胞を活性化し,マウスT細胞をin vitroにおいてSEEで感作したところ,CD8細胞のみVβ特異的にトレランスが誘導された.スーパー抗原活性を持つ新しい外毒素としてY.pseudotuberculosisからYPMを発見した.マウスT細胞のSEA応答性はアクセサリー細胞の種類により異なった.マウスSEA投与によるT細胞アナジーの誘導は,IL-2の早期に枯渇した.ヒト臍帯血T細胞や胸腺中CD4+T細胞は成人末梢血T細胞と異なり,スーパー抗原に対してアナジーになりやすかった.マウス胸腺NKT細胞の中の特殊なタイプH4という新しく発見された少し異なるco-stimulatorの機能を持つ分化抗原を発見した
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東京女子医科大学雑誌, 71(11) 845-845, Dec 25, 2001
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FASEB JOURNAL, 14(6) A967-A967, Apr, 2000
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東京女子医科大学雑誌, 69(12) 730-730, Dec 25, 1999
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日本免疫学会総会・学術集会記録, 29 168, Oct 30, 1999
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FASEB JOURNAL, 13(5) A987-A987, Mar, 1999
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FASEB JOURNAL, 13(4) A330-A330, Mar, 1999
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21 523-523, Dec 1, 1998
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Collected papers from the Institute of Immunological Science Hokkaido University, 18 5-10, 1995
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Collected papers from the Institute of Immunological Science Hokkaido University, 18 11-13, 1995
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Collected papers from the Institute of Immunological Science Hokkaido University, 17 8-12, 1994
Presentations
26Teaching Experience
11Professional Memberships
2Research Projects
5-
科研費 基盤C, 文科省, 2022 - 2024
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科研費 基盤C, 文科省, 2018 - 2020
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Grants-in-Aid for Scientific Research, Japan Society for the Promotion of Science, 2009 - 2011
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Grants-in-Aid for Scientific Research, Japan Society for the Promotion of Science, 2004 - 2005
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科学研究費助成事業, 日本学術振興会, 2002 - 2003