| First Author | Lv L | Year | 2023 |
| Journal | PLoS Pathog | Volume | 19 |
| Issue | 4 | Pages | e1011314 |
| PubMed ID | 37023217 | Mgi Jnum | J:340264 |
| Mgi Id | MGI:7465828 | Doi | 10.1371/journal.ppat.1011314 |
| Citation | Lv L, et al. (2023) Selenoprotein K enhances STING oligomerization to facilitate antiviral response. PLoS Pathog 19(4):e1011314 |
| abstractText | Stimulator-of-interferon gene (STING) is a vital element of the innate immune system against DNA viruses. Optimal activation of STING is crucial for maintaining immune homeostasis and eliminating invading viruses, and the oligomerization of STING is an essential prerequisite for STING activation. However, the mechanism of cGAMP-induced STING oligomerization in ER remains unclear. Selenoproteins are crucial for various physiological processes. Here, we identified that the endoplasmic reticulum (ER)-located transmembrane selenoprotein K (SELENOK) was induced during virus infection and facilitated innate immune responses against herpes simplex virus-1 (HSV-1). Mechanistically, SELENOK interacts with STING in the ER and promotes STING oligomerization, which in turn promotes its translocation from the ER to the Golgi. Consequently, Selenok deficiency suppresses STING-dependent innate responses and facilitates viral replication in vivo. Thus, the control of STING activation by selenium-mediated SELENOK expression will be a priming therapeutic strategy for the treatment of STING-associated diseases. |
