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吸烟产品通过其受体的磷酸化依赖性下调来抑制I型干扰素的抗病毒作用。

Cigarette smoking products suppress anti-viral effects of Type I interferon via phosphorylation-dependent downregulation of its receptor.

作者信息

HuangFu Wei-Chun, Liu Jianghuai, Harty Ronald N, Fuchs Serge Y

机构信息

Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Room 316, Hill Pavilion, 380 South University Avenue, Philadelphia, PA 19104-4539, USA.

出版信息

FEBS Lett. 2008 Sep 22;582(21-22):3206-10. doi: 10.1016/j.febslet.2008.08.013. Epub 2008 Aug 21.

Abstract

While negative effect of smoking on the resistance to viral infections was known, the underlying mechanisms remained unclear. Here we report that products of cigarette smoking compromise the cellular anti-viral defenses by inhibiting the signaling induced by Type I interferon (IFN). Cigarette smoking condensate (but not pure nicotine) stimulated specific serine phosphorylation-dependent ubiquitination and degradation of the IFNAR1 subunit of the Type I IFN receptor leading to attenuation of IFN signaling and decreased resistance to viral infection. This resistance was restored in cells where phosphorylation-dependent degradation of IFNAR1 is abolished. We conclude that smoking compromises cellular anti-viral defenses via degradation of Type I IFN receptor and discuss the significance of this mechanism for efficacy of IFN-based therapies.

摘要

虽然吸烟对病毒感染抵抗力的负面影响是已知的,但其潜在机制仍不清楚。在此我们报告,吸烟产物通过抑制I型干扰素(IFN)诱导的信号传导来损害细胞抗病毒防御。吸烟冷凝物(而非纯尼古丁)刺激I型IFN受体的IFNAR1亚基发生特异性丝氨酸磷酸化依赖性泛素化和降解,导致IFN信号减弱以及对病毒感染的抵抗力降低。在IFNAR1磷酸化依赖性降解被消除的细胞中,这种抵抗力得以恢复。我们得出结论,吸烟通过I型IFN受体的降解损害细胞抗病毒防御,并讨论了该机制对基于IFN疗法疗效的意义。

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