dc.contributor.author | Richards, Alexsia | |
dc.contributor.author | Friesen, Max | |
dc.contributor.author | Khalil, Andrew | |
dc.contributor.author | Barrasa, M Inmaculada | |
dc.contributor.author | Gehrke, Lee | |
dc.contributor.author | Jaenisch, Rudolf | |
dc.date.accessioned | 2022-12-12T14:37:44Z | |
dc.date.available | 2022-12-12T14:37:44Z | |
dc.date.issued | 2022-10 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/146839 | |
dc.description.abstract | Although 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.iso | en | |
dc.publisher | Elsevier BV | en_US |
dc.relation.isversionof | 10.1016/j.isci.2022.105146 | en_US |
dc.rights | Creative Commons Attribution 4.0 International license | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
dc.source | Elsevier | en_US |
dc.title | SARS-CoV-2 infection of human pluripotent stem cell-derived liver organoids reveals potential mechanisms of liver pathology | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Richards, 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.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.relation.journal | iScience | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2022-12-12T14:31:29Z | |
dspace.orderedauthors | Richards, A; Friesen, M; Khalil, A; Barrasa, MI; Gehrke, L; Jaenisch, R | en_US |
dspace.date.submission | 2022-12-12T14:31:31Z | |
mit.journal.volume | 25 | en_US |
mit.journal.issue | 10 | en_US |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Authority Work and Publication Information Needed | en_US |