酪氨酸激酶2
银屑病
体内
酪氨酸激酶
免疫系统
激酶
炎症
免疫学
化学
生物
细胞生物学
信号转导
受体
生物化学
血小板源性生长因子受体
生物技术
生长因子
作者
Masayuki Ishizaki,Toshihiko Akimoto,Ryuta Muromoto,Mika Yokoyama,Y. Ohshiro,Yuichi Sekine,Hiroaki Maeda,Kazuya Shimoda,Kenji Oritani,Tadashi Matsuda
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2011-05-24
卷期号:187 (1): 181-189
被引量:107
标识
DOI:10.4049/jimmunol.1003244
摘要
Tyrosine kinase-2 (Tyk2), a member of the Jak family of kinases, mediates the signals triggered by various cytokines, including type I IFNs, IL-12, and IL-23. In the current study, we investigated the in vivo involvement of Tyk2 in several IL-12/Th1- and IL-23/Th17-mediated models of experimental diseases, including methylated BSA injection-induced footpad thickness, imiquimod-induced psoriasis-like skin inflammation, and dextran sulfate sodium- or 2,4,6-trinitrobenzene sulfonic acid-induced colitis. In these disease models, Tyk2 deficiency influenced the phenotypes in immunity and/or inflammation. Our findings demonstrate a somewhat broader contribution of Tyk2 to immune systems than previously expected and suggest that Tyk2 may represent an important candidate for drug development by targeting both the IL-12/Th1 and IL-23/Th17 axes.
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