Schneider Andrea, Reichart Ursula, Gerner Wilhelm, Kolbe Thomas, Saalmüller Armin, Müller Mathias
Institute of Animal Breeding and Genetics, University of Veterinary Medicine, Veterinaerplatz 1, A-1210 Vienna, Austria.
FEBS Lett. 2008 Oct 29;582(25-26):3681-6. doi: 10.1016/j.febslet.2008.09.053. Epub 2008 Oct 7.
Tyk2 deficient mice show a markedly reduced susceptibility to lipopolysaccharide (LPS) induced shock and a partial impairment of IL-12 and interferon (IFN) signals. To examine the underlying mechanisms, we analysed the activation of peritoneal macrophages (PMPhis) and spleen cells after LPS challenge. In PMPhis and spleen cells the contribution of Tyk2 to the induction of the T-cell co-stimulatory molecules CD86, CD40 and MHC II was small or insignificant. By contrast, induced expression of the early activation marker CD69 on PMPhis and splenic cell populations required type I interferons (IFN-I) and Tyk2. The data suggest a selective contribution of Tyk2 to the activation of inflammation-relevant cell types by LPS.
酪氨酸激酶2(Tyk2)缺陷小鼠对脂多糖(LPS)诱导的休克敏感性显著降低,且白细胞介素12(IL-12)和干扰素(IFN)信号存在部分缺陷。为了研究潜在机制,我们分析了LPS刺激后腹腔巨噬细胞(PMPhis)和脾细胞的活化情况。在PMPhis和脾细胞中,Tyk2对T细胞共刺激分子CD86、CD40和主要组织相容性复合体II类(MHC II)诱导的贡献很小或不显著。相比之下,PMPhis和脾细胞群体上早期活化标志物CD69的诱导表达需要I型干扰素(IFN-I)和Tyk2。数据表明Tyk2对LPS激活炎症相关细胞类型具有选择性作用。