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WFDC1/ps20:影响中性粒细胞对鼠肝炎病毒(MHV)1 感染反应的宿主因子。

WFDC1/ps20: a host factor that influences the neutrophil response to murine hepatitis virus (MHV) 1 infection.

机构信息

Toronto General Research Institute, Division of Cell and Molecular Biology, University Health Network, 67 College Street, Toronto, Ontario, Canada M5G 2M1.

出版信息

Antiviral Res. 2012 Nov;96(2):158-68. doi: 10.1016/j.antiviral.2012.08.012. Epub 2012 Sep 6.

Abstract

The whey acidic protein family member, WFDC1/ps20 is a permissivity factor in HIV infection. Herein we describe a contrasting role for ps20 in limiting MHV-1 infection. Intranasal MHV-1 infection produces a respiratory infection in mice. Using ps20 knockout mice we provide evidence that intranasal MHV-1 infection results in increased lung viral titers in ps20(-/-) compared to ps20(+/+) mice. Accompanying MHV-1 infection we observe an increase in the number of neutrophils infiltrating the BAL and an increase in the percentage of neutrophils in the lung draining lymph nodes of ps20(-/-) compared with ps20(+/+) mice. Gene expression levels for the neutrophil chemoattractants CXCL1 and CXCL2 are elevated in the lungs of ps20(-/-) mice post-MHV-1 infection. Characterization of the immune cell profile in naïve ps20(-/-) mice revealed an increase in circulating neutrophils compared to ps20(+/+) mice. No notable differences in other immune cell profiles were observed between the ps20(+/+) and ps20(-/-) mice. Accordingly, we examined MHV-1 infection of neutrophils and provide evidence that neutrophils isolated from ps20(-/-) mice are more susceptible to MHV-1 infection than neutrophils isolated from ps20(+/+) mice. These data suggest roles for ps20 in regulating expression of neutrophil-specific chemotactic factors, thereby potentially modulating neutrophil migration, and in modulating neutrophil susceptibility to MHV-1 infection.

摘要

乳清白蛋白酸性蛋白家族成员 WFDC1/ps20 是 HIV 感染的许可因子。在此,我们描述了 ps20 在限制 MHV-1 感染方面的对比作用。鼻内 MHV-1 感染会导致小鼠发生呼吸道感染。使用 ps20 敲除小鼠,我们提供了证据表明,与 ps20(+/+)小鼠相比,鼻内 MHV-1 感染会导致 ps20(-/-)小鼠肺部病毒滴度增加。伴随 MHV-1 感染,我们观察到流入 BAL 的嗜中性粒细胞数量增加,并且 ps20(-/-)小鼠肺部引流淋巴结中的嗜中性粒细胞百分比增加。与 ps20(+/+)小鼠相比,MHV-1 感染后 ps20(-/-)小鼠肺部中性粒细胞趋化因子 CXCL1 和 CXCL2 的基因表达水平升高。在未感染的 ps20(-/-)小鼠中,特征在于循环中性粒细胞的增加与 ps20(+/+)小鼠相比。在 ps20(+/+)和 ps20(-/-)小鼠之间,未观察到其他免疫细胞谱之间存在明显差异。因此,我们检查了 MHV-1 对中性粒细胞的感染,并提供了证据表明,与 ps20(+/+)小鼠分离的中性粒细胞相比,从 ps20(-/-)小鼠分离的中性粒细胞更容易感染 MHV-1。这些数据表明 ps20 在调节中性粒细胞特异性趋化因子的表达中起作用,从而可能调节中性粒细胞的迁移,并调节中性粒细胞对 MHV-1 感染的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/7114264/e0be54b3227a/gr1ab.jpg

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