| First Author | Meng Q | Year | 2015 |
| Journal | J Cell Biol | Volume | 211 |
| Issue | 5 | Pages | 1025-40 |
| PubMed ID | 26620909 | Mgi Jnum | J:230731 |
| Mgi Id | MGI:5763688 | Doi | 10.1083/jcb.201505091 |
| Citation | Meng Q, et al. (2015) Reversible ubiquitination shapes NLRC5 function and modulates NF-kappaB activation switch. J Cell Biol 211(5):1025-40 |
| abstractText | NLRC5 is an important regulator in innate immune responses. However, the ability of NLRC5 to inhibit NF-kappaB activation is controversial in different cell types. How dynamic modification of NLRC5 shapes NF-kappaB signaling remains unknown. We demonstrated that NLRC5 undergoes robust ubiquitination by TRAF2/6 after lipopolysaccharide treatment, which leads to dissociation of the NLRC5-IkappaB kinase complex. Experimental and mathematical analyses revealed that the K63-linked ubiquitination of NLRC5 at lysine 1,178 generates a coherent feedforward loop to further sensitize NF-kappaB activation. Meanwhile, we found USP14 specifically removes the polyubiquitin chains from NLRC5 to enhance NLRC5-mediated inhibition of NF-kappaB signaling. Furthermore, we found that different cell types may exhibit different sensitivities to NF-kappaB activation in response to NLRC5 ablation, possibly as a result of the various intrinsic levels of deubiquitinases and NLRC5. This might partially reconcile controversial studies and explain why NLRC5 exhibits diverse inhibitory efficiencies. Collectively, our results provide the regulatory mechanisms of reversible NLRC5 ubiquitination and its role in the dynamic control of innate immunity. |
