- Browse by Author
Browsing by Author "Vanaja, Sivapriya Kailasan"
Now showing 1 - 1 of 1
Results Per Page
Sort Options
Item UBXN9 governs GLUT4-mediated spatial confinement of RIG-I-like receptors and signaling(Research Square, 2024-06-04) Wang, Penghua; Harrison, Andrew; Yang, Duomeng; Cahoon, Jason; Geng, Tingting; Cao, Ziming; Karginov, Timofey; Chiari, Conner; Li, Xin; Qyang, Yibing; Vella, Anthony; Fan, Zhichao; Vanaja, Sivapriya Kailasan; Rathinam, Vijay; Witczak, Carol; Bogan, Jonathan; Cellular and Integrative Physiology, School of MedicineThe cytoplasmic RIG-I-like receptors (RLRs) recognize viral RNA and initiate innate antiviral immunity. RLR signaling also triggers glycolytic reprogramming through glucose transporters (GLUTs), whose role in antiviral immunity is elusive. Here, we unveil that insulin-responsive GLUT4 inhibits RLR signaling independently of glucose uptake in adipose and muscle tissues. At steady state, GLUT4 is docked at the Golgi matrix by ubiquitin regulatory X domain 9 (UBXN9, TUG). Following RNA virus infection, GLUT4 is released and translocated to the cell surface where it spatially segregates a significant pool of cytosolic RLRs, preventing them from activating IFN-β responses. UBXN9 deletion prompts constitutive GLUT4 trafficking, sequestration of RLRs, and attenuation of antiviral immunity, whereas GLUT4 deletion heightens RLR signaling. Notably, reduced GLUT4 expression is uniquely associated with human inflammatory myopathies characterized by hyperactive interferon responses. Overall, our results demonstrate a noncanonical UBXN9-GLUT4 axis that controls antiviral immunity via plasma membrane tethering of cytosolic RLRs.