Phospholipase A2 inhibitor and LY6/PLAUR domain-containing protein PINLYP regulates type I interferon innate immunity.
Zhongshun LiuCongwei JiangZhangmengxue LeiSihan DongLinlin KuangChenxu HuangYing GaoMu LiuHui XiaoPatrick LegembreJae U JungHuaping LiangXiaozhen LiangPublished in: Proceedings of the National Academy of Sciences of the United States of America (2022)
Type I interferons (IFNs) are the first frontline of the host innate immune response against invading pathogens. Herein, we characterized an unknown protein encoded by phospholipase A2 inhibitor and LY6/PLAUR domain-containing (PINLYP) gene that interacted with TBK1 and induced type I IFN in a TBK1- and IRF3-dependent manner. Loss of PINLYP impaired the activation of IRF3 and production of IFN-β induced by DNA virus, RNA virus, and various Toll-like receptor ligands in multiple cell types. Because PINLYP deficiency in mice engendered an early embryonic lethality in mice, we generated a conditional mouse in which PINLYP was depleted in dendritic cells. Mice lacking PINLYP in dendritic cells were defective in type I IFN induction and more susceptible to lethal virus infection. Thus, PINLYP is a positive regulator of type I IFN innate immunity and important for effective host defense against viral infection.
Keyphrases
- dendritic cells
- immune response
- toll like receptor
- regulatory t cells
- high fat diet induced
- nuclear factor
- gene expression
- single cell
- insulin resistance
- protein protein
- inflammatory response
- stem cells
- small molecule
- diabetic rats
- transcription factor
- copy number
- cell free
- type diabetes
- single molecule
- dna methylation
- mesenchymal stem cells
- amino acid
- nucleic acid
- antimicrobial resistance
- drug induced
- multidrug resistant
- gram negative
- circulating tumor cells
- disease virus
- smoking cessation