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dc.contributor.authorVladimer, Gregory I.
dc.contributor.authorMarty-Roix, Robyn Lynn
dc.contributor.authorGhosh, Shubhendu
dc.contributor.authorWeng, Dan
dc.contributor.authorLien, Egil
dc.date2022-08-11T08:08:54.000
dc.date.accessioned2022-08-23T16:11:52Z
dc.date.available2022-08-23T16:11:52Z
dc.date.issued2013-01-11
dc.date.submitted2013-01-27
dc.identifier.citationCurr Opin Microbiol. 2013 Jan 11. doi: 10.1016/j.mib.2012.11.008.
dc.identifier.issn1879-0364
dc.identifier.doi10.1016/j.mib.2012.11.008
dc.identifier.pmid23318142
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33270
dc.description.abstractThe inflammasome has emerged as an important molecular protein complex which initiates proteolytic processing of pro-IL-1β and pro-IL-18 into mature inflammatory cytokines. In addition, inflammasomes initiate pyroptotic cell death that may be independent of those cytokines. Inflammasomes are central to elicit innate immune responses against many pathogens, and are key components in the induction of host defenses following bacterial infection. Here, we review recent discoveries related to NLRP1, NLRP3, NLRC4, NLRP6, NLRP7, NLRP12 and AIM2-mediated recognition of bacteria. Mechanisms for inflammasome activation and regulation are now suggested to involve kinases such as PKR and PKCδ, ligand binding proteins such as the NAIPs, and caspase-11 and caspase-8 in addition to caspase-1. Future research will determine how specific inflammasome components pair up in optimal responses to specific bacteria.
dc.language.isoen_US
dc.publisherCurrent Biology
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=23318142&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.mib.2012.11.008
dc.subjectInflammasomes; Bacterial Infections
dc.subjectImmunology and Infectious Disease
dc.titleInflammasomes and host defenses against bacterial infections
dc.typeJournal Article
dc.source.journaltitleCurrent opinion in microbiology
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1802
dc.identifier.contextkey3619603
html.description.abstract<p>The inflammasome has emerged as an important molecular protein complex which initiates proteolytic processing of pro-IL-1β and pro-IL-18 into mature inflammatory cytokines. In addition, inflammasomes initiate pyroptotic cell death that may be independent of those cytokines. Inflammasomes are central to elicit innate immune responses against many pathogens, and are key components in the induction of host defenses following bacterial infection. Here, we review recent discoveries related to NLRP1, NLRP3, NLRC4, NLRP6, NLRP7, NLRP12 and AIM2-mediated recognition of bacteria. Mechanisms for inflammasome activation and regulation are now suggested to involve kinases such as PKR and PKCδ, ligand binding proteins such as the NAIPs, and caspase-11 and caspase-8 in addition to caspase-1. Future research will determine how specific inflammasome components pair up in optimal responses to specific bacteria.</p>
dc.identifier.submissionpathgsbs_sp/1802
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.contributor.studentGregory Vladimer; Dan Weng


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