| First Author | Gurung P | Year | 2015 |
| Journal | J Immunol | Volume | 194 |
| Issue | 5 | Pages | 2064-7 |
| PubMed ID | 25637014 | Mgi Jnum | J:296049 |
| Mgi Id | MGI:6466767 | Doi | 10.4049/jimmunol.1402951 |
| Citation | Gurung P, et al. (2015) Cutting edge: SHARPIN is required for optimal NLRP3 inflammasome activation. J Immunol 194(5):2064-7 |
| abstractText | The NLRP3 inflammasome is a multimeric protein complex that is assembled in response to a wide array of pathogens and danger-associated molecular patterns. Despite the ability of NLRP3 to respond to diverse cues, the mechanisms controlling the assembly of this complex are contested. Recently published studies showed that HOIL-1, a member of the linear ubiquitin chain assembly complex, contributes to activation of the NLRP3 inflammasome. SHARPIN, along with HOIP and HOIL-1, constitute the linear ubiquitin chain assembly complex. In this study, we examined whether SHARPIN is required for the activation of the NLRP3 inflammasome. Using Sharpin(cpdm) macrophages (deficient in SHARPIN expression), we demonstrate that SHARPIN is required for optimal activation of the NLRP3 inflammasome by both canonical and noncanonical stimuli. Furthermore, Sharpin(cpdm) macrophages had dramatic defects on both the NF-kappaB and MAPK pathways, suggesting a role in transcriptional priming of the NLRP3 inflammasome. In conclusion, our study identified SHARPIN as a novel regulator of the NLRP3 inflammasome. |
