Studies on narcolepsy by orexin/HLA class II complex
Project/Area Number |
18K19450
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Research Category |
Grant-in-Aid for Challenging Research (Exploratory)
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Allocation Type | Multi-year Fund |
Review Section |
Medium-sized Section 49:Pathology, infection/immunology, and related fields
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Research Institution | Osaka University |
Principal Investigator |
Arase Hisashi 大阪大学, 微生物病研究所, 教授 (10261900)
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Project Period (FY) |
2018-06-29 – 2021-03-31
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Project Status |
Completed (Fiscal Year 2020)
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Budget Amount *help |
¥6,240,000 (Direct Cost: ¥4,800,000、Indirect Cost: ¥1,440,000)
Fiscal Year 2019: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Fiscal Year 2018: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
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Keywords | HLAクラスII / オレキシン / エクソゾーム / HLA クラスII / HLAクラスⅡ |
Outline of Final Research Achievements |
rexin was also found to form a complex with HLA-DQ0602, an allele susceptible to narcolepsy. In contrast, only weak complex formation was observed with the non-sensitive allele. Therefore, it is possible that the cytotoxicity caused by the formation of orexin complexes with HLA-DQ0602 and the interaction with orexin receptors are involved in the survival of orexin-producing cells in patients with narcolepsy. Therefore, we produced orexin-HLA class II complexes and analyzed the cytotoxicity of the complexes. However, no cytotoxicity of the complex was observed in cultured cells. In the future, it will be necessary to analyze the toxicity of the complex using neurons and other cells.
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Academic Significance and Societal Importance of the Research Achievements |
ナルコレプシーは神経変性疾患の一つであり、オレキシン産生細胞が欠落してしまう疾患であるが、原因は不明である。一方、ナルコレプシーはHLA-DQ0602の遺伝子アリルを持っている人のみが発症する。本研究により、初めてオレキシンがHLA-DQ0602の複合体を形成することが判明した。オレキシン・HLA-DQ0602複合体の詳細な機能までは明らかにできなかったが、今後、オレキシン・HLA-DQ0602複合体の機能の研究を進めることで、ナルコレプシーの発症機構や治療法の開発が可能になることが期待される。
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Report
(4 results)
Research Products
(50 results)
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[Journal Article] The beta(2)-Glycoprotein I/HLA-DR Complex As A Major Autoantibody Target in Obstetric Antiphospholipid Syndrome2020
Author(s)
[Kenji Tanimura,Shigeru Saito,Mikiya Nakatsuka,Takeshi Nagamatsu,Tomoyuki Fujii,Atsushi Fukui,Masashi Deguchi,Yuki Sasagawa,Noriko Arase,Hisashi Arase,Hideto Yamada]
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Journal Title
ARTHRITIS & RHEUMATOLOGY
Volume: 72
Issue: 11
Pages: 1882-1891
DOI
Related Report
Peer Reviewed
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[Journal Article] Autoantibodies detected in patients with vitiligo vulgaris but not in those with rhododendrol-induced leukoderma2019
Author(s)
Arase Noriko,Tanemura Atsushi,Jin Hui,Nishioka Megumi,Aoyama Yumi,Oiso Naoki,Matsunaga Kayoko,Suzuki Tamio,Nishigori Chikako,Kawamura Tatsuyoshi,Shimizu Tadamichi,Ito Akiko,Fukai Kazuyoshi,Abe Yuko,Yang Lingli,Tsuruta Daisuke,et al
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Journal Title
Journal of Dermatological Science
Volume: 95
Issue: 2
Pages: 80-83
DOI
Related Report
Peer Reviewed
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[Journal Article] Blocking immunoinhibitory receptor LILRB2 reprograms tumor-associated myeloid cells and promotes antitumor immunity.2018
Author(s)
Chen HM, van der Touw W, Wang YS, Kang K, Mai S, Zhang J, Alsina-Beauchamp D, Duty JA, Mungamuri SK, Zhang B, Moran T, Flavell R, Aaronson S, Hu HM, Arase H, Ramanathan S, Flores R, Pan PY, Chen SH.
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Journal Title
J. Clin. Invest.
Volume: 128
Issue: 12
Pages: 5647-5662
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] LILRB4 signalling in leukaemia cells mediates T cell suppression and tumour infiltration.2018
Author(s)
Deng M, 外30名, Arase H, Xia N, Jiang Y, Collins R, You MJ, Homsi J, Unni N, Lewis C, Chen GQ, Fu YX, Liao XC, An Z, Zheng J, Zhang N, Zhang CC.
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Journal Title
Nature.
Volume: 562
Issue: 7728
Pages: 605-609
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Heme ameliorates dextran sodium sulfate-induced colitis through providing intestinal macrophages with noninflammatory profiles.2018
Author(s)
Kayama H, Kohyama M, Okuzaki D, Motooka D, Barman S, Okumura R, Muneta M, Hoshino K, Sasaki I, Ise W, Matsuno H, Nishimura J, Kurosaki T, Nakamura S, Arase H, Kaisho T, Takeda K.
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Journal Title
Proc Natl Acad Sci U S A.
Volume: 115
Issue: 33
Pages: 8418-8423
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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