Cell biology of inflammasome activation
| dc.contributor.author | Pandey, Abhimanu | |
| dc.contributor.author | Shen, Cheng | |
| dc.contributor.author | Feng, Shouya | |
| dc.contributor.author | Man, Si Ming | |
| dc.date.accessioned | 2023-03-31T03:43:12Z | |
| dc.date.issued | 2021 | |
| dc.date.updated | 2022-01-16T07:21:41Z | |
| dc.description.abstract | Organelles are critical structures in mediating the assembly and activation of inflammasomes in mammalian cells, resulting in inflammation and cell death. Assembly of inflammasomes can occur at the mitochondria, endoplasmic reticulum, nucleus, trans-Golgi network, or pathogen surface, facilitated by the overarching architecture of the cytoskeleton. NLRP3 and Pyrin inflammasome sensors may form smaller speckles and converge on a single larger speck at the microtubule-organizing center or MTOC. This signaling hub activates multiple mammalian inflammatory and apoptotic caspases, cytokine substrates, the pore-forming protein gasdermin D, and the plasma membrane rupture protein ninjurin-1 or NINJ1, allowing pyroptosis, cellular disintegration, and inflammation to ensue. In this review, we highlight the role of mammalian cell types and organellar architectures in executing inflammasome responses. | en_AU |
| dc.description.sponsorship | S.M.M. is supported by The Australian National University, the CSL Centenary Fellowship, and the National Health and Medical Research Council of Australia under Grants APP1141504, APP1162103, APP1163358, and APP2002686. A.P., and S.F. are supported by The Gretel and Gordon Bootes Medical Research Foundation. A.P., C.S., and S.F. are supported by The John Curtin School of Medical Research International Ph.D. scholarships. | en_AU |
| dc.format.mimetype | application/pdf | en_AU |
| dc.identifier.issn | 0962-8924 | en_AU |
| dc.identifier.uri | http://hdl.handle.net/1885/287928 | |
| dc.language.iso | en_AU | en_AU |
| dc.provenance | https://v2.sherpa.ac.uk/id/publication/23055..."The Accepted Version can be archived in an Institutional Repository. 12 Months. CC BY-NC-ND." from SHERPA/RoMEO site (as at 5/04/2023). | |
| dc.publisher | Elsevier BV | en_AU |
| dc.relation | http://purl.org/au-research/grants/nhmrc/1141504 | en_AU |
| dc.relation | http://purl.org/au-research/grants/nhmrc/GNT1162103 | en_AU |
| dc.relation | http://purl.org/au-research/grants/nhmrc/GNT1163358 | en_AU |
| dc.relation | http://purl.org/au-research/grants/nhmrc/2002686 | en_AU |
| dc.rights | © 2021 Elsevier Ltd. | en_AU |
| dc.rights.license | CC BY-NC-ND | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.source | Trends in Cell Biology | en_AU |
| dc.title | Cell biology of inflammasome activation | en_AU |
| dc.type | Journal article | en_AU |
| dcterms.accessRights | Open Access | |
| local.bibliographicCitation.issue | 11 | en_AU |
| local.bibliographicCitation.lastpage | 939 | en_AU |
| local.bibliographicCitation.startpage | 924 | en_AU |
| local.contributor.affiliation | Pandey, Abhimanu, College of Health and Medicine, ANU | en_AU |
| local.contributor.affiliation | Shen, Cheng, College of Health and Medicine, ANU | en_AU |
| local.contributor.affiliation | Feng, Shouya, College of Health and Medicine, ANU | en_AU |
| local.contributor.affiliation | Man, Si Ming, College of Health and Medicine, ANU | en_AU |
| local.contributor.authoruid | Pandey, Abhimanu, u6566970 | en_AU |
| local.contributor.authoruid | Shen, Cheng, u6618716 | en_AU |
| local.contributor.authoruid | Feng, Shouya, u1043633 | en_AU |
| local.contributor.authoruid | Man, Si Ming, u1036742 | en_AU |
| local.description.notes | Imported from ARIES | en_AU |
| local.identifier.absfor | 320407 - Innate immunity | en_AU |
| local.identifier.ariespublication | u1036742xPUB56 | en_AU |
| local.identifier.citationvolume | 31 | en_AU |
| local.identifier.doi | 10.1016/j.tcb.2021.06.010 | en_AU |
| local.publisher.url | https://www.cell.com/ | en_AU |
| local.type.status | Accepted Version | en_AU |
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