Show simple item record

dc.contributor.authorRichards, Alexsia
dc.contributor.authorFriesen, Max
dc.contributor.authorKhalil, Andrew
dc.contributor.authorBarrasa, M Inmaculada
dc.contributor.authorGehrke, Lee
dc.contributor.authorJaenisch, Rudolf
dc.date.accessioned2022-12-12T14:37:44Z
dc.date.available2022-12-12T14:37:44Z
dc.date.issued2022-10
dc.identifier.urihttps://hdl.handle.net/1721.1/146839
dc.description.abstractAlthough respiratory symptoms are the most prevalent disease manifestation of infection by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), infection can also damage other organs, including the brain, gut, and liver. Symptoms of liver damage are observed in nearly half of patients that succumb to severe SARS-CoV-2 infection. Here we use human-induced pluripotent stem cell-derived liver organoids (HLOs) to recapitulate and characterize liver pathology following virus exposure. Utilizing single-cell sequencing technology, we identified robust transcriptomic changes that occur in SARS-CoV-2 infected liver cells as well as uninfected bystander cells. Our results show a significant induction of many inflammatory pathways, including IFN-α, INF-γ, and IL-6 signaling. Our results further identify IL-6 signaling as a potential mechanism for liver-mediated activation of circulating macrophages.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionof10.1016/j.isci.2022.105146en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElsevieren_US
dc.titleSARS-CoV-2 infection of human pluripotent stem cell-derived liver organoids reveals potential mechanisms of liver pathologyen_US
dc.typeArticleen_US
dc.identifier.citationRichards, Alexsia, Friesen, Max, Khalil, Andrew, Barrasa, M Inmaculada, Gehrke, Lee et al. 2022. "SARS-CoV-2 infection of human pluripotent stem cell-derived liver organoids reveals potential mechanisms of liver pathology." iScience, 25 (10).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journaliScienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-12T14:31:29Z
dspace.orderedauthorsRichards, A; Friesen, M; Khalil, A; Barrasa, MI; Gehrke, L; Jaenisch, Ren_US
dspace.date.submission2022-12-12T14:31:31Z
mit.journal.volume25en_US
mit.journal.issue10en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record