Unknown

Dataset Information

0

SARS-CoV-2 infection of human pluripotent stem cell-derived liver organoids reveals potential mechanisms of liver pathology.


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.

SUBMITTER: Richards A 

PROVIDER: S-EPMC9477603 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

SARS-CoV-2 infection of human pluripotent stem cell-derived liver organoids reveals potential mechanisms of liver pathology.

Richards Alexsia A   Friesen Max M   Khalil Andrew A   Barrasa M Inmaculada MI   Gehrke Lee L   Jaenisch Rudolf R  

iScience 20220916 10


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. Utiliz  ...[more]

Similar Datasets

2022-10-04 | GSE210061 | GEO
2022-10-04 | GSE210059 | GEO
2022-10-04 | GSE210058 | GEO
| PRJNA863578 | ENA
| S-EPMC9637521 | biostudies-literature
| S-EPMC11580836 | biostudies-literature
| PRJNA863583 | ENA
| S-EPMC8550698 | biostudies-literature
| S-EPMC8895131 | biostudies-literature
| PRJNA863584 | ENA