2013 Fiscal Year Final Research Report
Macrophage function and polymorphism of PKCeta in neuromyelitis optica and multiple sclerosis
Project/Area Number |
23591247
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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 |
Neurology
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Research Institution | Kyushu University |
Principal Investigator |
MATSUSHITA Takuya 九州大学, 医学(系)研究科(研究院), 研究員 (00533001)
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Co-Investigator(Kenkyū-buntansha) |
YOSHIMURA Satoshi 九州大学, 大学院医学研究院神経内科学, 共同研究員 (20596390)
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Project Period (FY) |
2011 – 2013
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Keywords | 多発性硬化症 / 視神経脊髄炎 / マクロファージ / PRKCH |
Research Abstract |
Polymorphism of PKCeta (rs2230500) was not risk allele or disease modulation factor for multiple sclerosis (MS) or neuromyelitis optica (NMO). However, a ratio of CX3CR1 positive monocytes was increased in rs2230500-A positive group of MS without therapy than in the allele-negative group. From a measurement of cytokines/chemokines of CSF revealed that CXCL8 was increased in rs2230500- A positive group of MS at remission phase and primary progressive MS than in the allele-negative group. These findings suggest differences of function of macrophages or microglia between PKCeta polymorphisms.
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[Presentation] Cytokine receptor expressions in monocyte subsets in multiple sclerosis, neuromyelitis optica, and amyotrophic lateral sclerosis2013
Author(s)
Cui YW, Kawano Y, Shi N, Masaki K, Isobe N, Yonekawa T, Matsushita T, Tateishi T, Yamasaki R, Kira J
Organizer
PACTRIMS
Place of Presentation
Kyoto
Year and Date
20131106-08
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