Hasebe Rie, Suzuki Akio, Yamasaki Takeshi, Horiuchi Motohiro
Laboratory of Veterinary Hygiene, Graduate School of Veterinary Medicine, Hokkaido University, Nishi 9, Kita 18, Kita-ku, Sapporo 060-0818, Japan.
Laboratory of Veterinary Hygiene, Graduate School of Veterinary Medicine, Hokkaido University, Nishi 9, Kita 18, Kita-ku, Sapporo 060-0818, Japan.
Biochem Biophys Res Commun. 2014 Nov 7;454(1):125-30. doi: 10.1016/j.bbrc.2014.10.043. Epub 2014 Oct 18.
CD14 deficient (CD14(-/-)) mice survived longer than wild-type (WT) C57BL/6J mice when inoculated with prions intracerebrally, accompanied by increased expression of anti-inflammatory cytokine IL-10 by microglia in the early stage of infection. To assess the immune regulatory effects of CD14 in detail, we compared the gene expression of pro- and anti-inflammatory cytokines in the brains of WT and CD14(-/-) mice infected with the Chandler strain. Gene expression of the anti-inflammatory cytokine IL-13 in prion-infected CD14(-/-) mice was temporarily upregulated at 75dpi, whereas IL-13 gene expression was not upregulated in prion-infected WT mice. Immunofluorescence staining showed that IL-13 was mainly expressed in neurons of the thalamus at 75dpi. These results suggest that CD14 can suppress IL-13 expression in neurons during the early stage of prion infection.
当脑内接种朊病毒时,CD14缺陷(CD14(-/-))小鼠比野生型(WT)C57BL/6J小鼠存活时间更长,在感染早期,小胶质细胞中抗炎细胞因子IL-10的表达增加。为了详细评估CD14的免疫调节作用,我们比较了感染钱德勒毒株的WT和CD14(-/-)小鼠大脑中促炎和抗炎细胞因子的基因表达。在朊病毒感染的CD14(-/-)小鼠中,抗炎细胞因子IL-13的基因表达在感染后75天(dpi)时暂时上调,而在朊病毒感染的WT小鼠中,IL-13基因表达未上调。免疫荧光染色显示,在75dpi时,IL-13主要在丘脑神经元中表达。这些结果表明,在朊病毒感染早期,CD14可抑制神经元中IL-13的表达。