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伪狂犬病病毒DNA与猪NLRC3结合可引发猪NLRP3炎性小体的激活。

Pseudorabies virus DNA binding to porcine NLRC3 unleashes the activation of the porcine NLRP3 inflammasome.

作者信息

Li Minjie, Huang Xiangyu, Yin Hongyan, Chai Lvye, Wang Haiwei, Li Xin

机构信息

National Key Laboratory of Veterinary Public Health and Safety, China Agricultural University, Beijing 100193, China; Key Laboratory of Animal Epidemiology of the Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing, China.

State Key Laboratory of Animal Disease Control, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.

出版信息

Vet Microbiol. 2025 Aug;307:110604. doi: 10.1016/j.vetmic.2025.110604. Epub 2025 Jun 13.

Abstract

Viral infection activates multiple inflammatory pathways, with the NLRP3 inflammasome playing a pivotal role in host defense. However, negative regulation of the NLRP3 inflammasome is essential for maintaining host homeostasis. Here, we report that double-stranded DNA (dsDNA) from pseudorabies virus (PRV) induces NLRP3 inflammasome activation and pyroptosis through gasdermin D (GSDMD) cleavage and IL-1β secretion. Importantly, the inhibitory NLR porcine NLRC3 (pNLRC3) interacts with porcine NLRP3 (pNLRP3) and attenuates GSDMD cleavage and IL-1β release. Upon PRV infection, overexpression of pNLRC3 enhances GSDMD cleavage and lactate dehydrogenase release, whereas knockdown of pNLRC3 reduces pyroptosis. Mechanistically, pNLRC3 binds PRV dsDNA and unleashes its inhibitory effect on pNLRP3, functioning as a checkpoint to regulate inflammasome activation. Furthermore, pNLRC3 contributes to PRV restriction by controlling viral replication and limiting infection. In summary, our findings reveal a dual role of pNLRC3, acting both as a negative regulator of the pNLRP3 inflammasome and as a viral sensor that regulates pyroptosis-mediated viral clearance. These insights provide a deeper understanding of virus-host interactions and innate immune regulation.

摘要

病毒感染会激活多种炎症途径,其中NLRP3炎性小体在宿主防御中起关键作用。然而,NLRP3炎性小体的负调控对于维持宿主机体稳态至关重要。在此,我们报道伪狂犬病病毒(PRV)的双链DNA(dsDNA)通过gasdermin D(GSDMD)裂解和IL-1β分泌诱导NLRP3炎性小体激活和细胞焦亡。重要的是,抑制性NLR猪NLRC3(pNLRC3)与猪NLRP3(pNLRP3)相互作用,并减弱GSDMD裂解和IL-1β释放。在PRV感染后,pNLRC3的过表达增强GSDMD裂解和乳酸脱氢酶释放,而pNLRC3的敲低则减少细胞焦亡。机制上,pNLRC3结合PRV dsDNA并释放其对pNLRP3的抑制作用,作为调节炎性小体激活的一个检查点发挥作用。此外,pNLRC3通过控制病毒复制和限制感染来促进对PRV的限制。总之,我们的研究结果揭示了pNLRC3的双重作用,它既是pNLRP3炎性小体的负调节因子,又是调节细胞焦亡介导的病毒清除的病毒传感器。这些见解为病毒-宿主相互作用和固有免疫调节提供了更深入的理解。

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