Single-cell transcriptomics stratifies organoid models of metabolic dysfunction-associated steatotic liver disease.
Ontology highlight
ABSTRACT: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a growing cause of morbidity with limited treatment options. Thus, accurate in vitro systems to test new therapies are indispensable. While recently, human liver organoid models have emerged to assess steatotic liver disease, a systematic evaluation of their translational potential is still missing. Here, we evaluated human liver organoid models of MASLD, comparatively testing disease induction in three conditions: oleic acid, palmitic acid, and TGF-β1. Through single-cell analyses, we find that all three models induce inflammatory signatures, but only TGF-β1 promotes collagen production, fibrosis, and hepatic stellate cell expansion. In striking contrast, oleic acid ameliorates fibrotic signatures and reduces the hepatic
SUBMITTER: Hess A
PROVIDER: S-EPMC10711666 | biostudies-literature | 2023 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA