Grass carp (Ctenopharyngodon idellus) SHP2 suppresses IFN I expression via decreasing the phosphorylation of GSK3β in a non-contact manner. Issue 116 (September 2021)

• Record Type: Journal Article
• Authors: Lu, Shina; Peng, Xiaojue; Lin, Gang; Xu, Kang; Wang, Shanghong; Qiu, Weihua; Du, Hailing; Chang, Kaile; Lv, Yangfeng; Liu, Yapeng; Deng, Hang; Hu, Chengyu; Xu, Xiaowen
• Is Part Of: Fish & shellfish immunology. Issue 116(2021)
• Page Start: 150
• Page End: 160
• Publication Date: 2021-09
• Subjects: SHP2 -- GSK3β-TBK1 axis -- Phosphorylation -- Innate immune -- Fish; Fishes -- Immunology -- Periodicals; Shellfish -- Immunology -- Periodicals; Poissons -- Immunologie -- Périodiques; Crustacés -- Immunologie -- Périodiques; 571.9617
• DOI: 10.1016/j.fsi.2021.07.005
• Languages: English
• ISSNs: 1050-4648

Abstract

Abstract: As a tyrosine phosphatase, Src homology 2-containing protein tyrosine phosphatase 2 (SHP2) serves as an inhibitor in PI3K-Akt pathway. In mammals, SHP2 can phosphorylate GSK3β at Y216 site to control the expression of IFN. So far, the multiple functions of SHP2 have been reported in mammals. However, little is known about fish SHP2. In this study, we cloned and identified a grass carp ( Ctenopharyngodon idellus ) SHP2 gene ( CiSHP2, MT373151). SHP2 is conserved among different vertebrates by amino acid sequences alignment and the phylogenetic tree analysis. CiSHP2 shared the closest homology with Danio rerio SHP2. Simultaneously, SHP2 was also tested in grass carp tissues and CIK ( C. idellus kidney) cells. We found that it responded to poly I:C stimulation. CiSHP2 was located in the cytoplasm just as the same as those of mammals. Interestingly, it inhibited the phosphorylation level of GSK3β in a non-contact manner. Meanwhile CiGSK3β interacted with and directly phosphorylated CiTBK1. In addition, we found that CiSHP2 also reduced the phosphorylation level of CiTBK1 by CiGSK3β, and then it depressed the expression of IFN I via GSK3β-TBK1 axis. These results suggested that CiSHP2 was involved in CiGSK3β and CiTBK1 activity but not regulated their transcriptional level. At the same time, we also found that CiSHP2 also influenced the activity of CiIRF3. Therefore, fish SHP2 inhibited IFN I expression through blocking GSK3β-TBK1 signal axis. Highlights: CiSHP2 responded to poly I:C stimulation and down-regulated CiIFN I expression. CiSHP2 didn't bind to CiGSK3β but could regulate its phosphorylation at Tyr 216 . CiGSK3β physically bound to CiTBK1 in the absence of poly I: C. Knocked-down of CiTBK1 can block the regulation of CiGSK3β on CiIFN I.