analysis of autoimmune disease caused by aging and sex hormones in a mouse model of sjogrens syndrome
| Project/Area Number |
18K17037
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| Research Category |
Grant-in-Aid for Early-Career Scientists
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| Allocation Type | Multi-year Fund |
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| Review Section |
Basic Section 57020:Oral pathobiological science-related
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| Research Institution | National Center for Geriatrics and Gerontology |
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Principal Investigator |
Kurosawa Mie 国立研究開発法人国立長寿医療研究センター, 口腔疾患研究部, 研究員 (70815802)
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| Project Period (FY) |
2018-04-01 – 2020-03-31
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| Project Status |
Completed (Fiscal Year 2019)
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| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2019: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2018: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | シェーグレン症候群 / 細胞老化 / 免疫老化 / 加齢 / エストロゲン欠乏 / 女性ホルモン |
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| Outline of Final Research Achievements |
Our objective was to elucidate the roles of aging and sex hormones in the pathogenesis of Sjogren’s syndrome. Senescence-associated CD4+ T (SA-T) cell numbers increase in secondary lymphoid organs with age. SA-T cells infiltrated the salivary glands (SG) of aged female mice. CXCL13 was more strongly expressed in the epithelial cells of the SG with age. TEM from aged mice demonstrated higher in vitro migratory activity toward CXCL13 than TEM from young mice. This study revealed that SA-T cells infiltrate the SG via CXCL13-CXCR5.
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| Academic Significance and Societal Importance of the Research Achievements |
シェーグレン症候群(SS)は外分泌腺を標的とする自己免疫疾患であり、中高年以降の女性に多く発症する。、SSは単独の因子によって起こるものではなく、性ホルモンのアンバランスや加齢による変化という身体的に大きな変化がどのようにしてSSの病態形成に関与するのかは不明である。そのため、加齢変化によって発症するSSやその他の自己免疫疾患などの病態解明の新たな一歩となる可能性がある。
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Report
(3 results)
Research Products
(7 results)
