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朊病毒感染早期,CD14缺陷小鼠大脑中抗炎细胞因子IL-13表达的暂时上调。

Temporary upregulation of anti-inflammatory cytokine IL-13 expression in the brains of CD14 deficient mice in the early stage of prion infection.

作者信息

Hasebe Rie, Suzuki Akio, Yamasaki Takeshi, Horiuchi Motohiro

机构信息

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.

出版信息

Biochem Biophys Res Commun. 2014 Nov 7;454(1):125-30. doi: 10.1016/j.bbrc.2014.10.043. Epub 2014 Oct 18.

Abstract

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.

摘要

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。

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