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Integrative analysis of single-cell RNA-seq and ATAC-seq reveals heterogeneity of induced pluripotent stem cell-derived hepatic organoids.
Kim, Jong-Hwan; Mun, Seon Ju; Kim, Jeong-Hwan; Son, Myung Jin; Kim, Seon-Young.
Afiliación
  • Kim JH; Korean Bioinformation Center, Daejeon, Korea.
  • Mun SJ; Stem Cell Convergence Research Center, Daejeon, Korea.
  • Kim JH; Department of Functional Genomics, University of Science and Technology (UST), Daejeon, Korea.
  • Son MJ; Personalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Korea.
  • Kim SY; Stem Cell Convergence Research Center, Daejeon, Korea.
iScience ; 26(9): 107675, 2023 Sep 15.
Article en En | MEDLINE | ID: mdl-37680467
ABSTRACT
To gain deeper insights into transcriptomes and epigenomes of organoids, liver organoids from two states (expandable and more differentiated) were subjected to single-cell RNA-seq (scRNA-seq) and single-cell ATAC-seq (scATAC-seq) analyses. Mitochondrial gene expression was higher in differentiated than in non-differentiated hepatocytes, with ATAC-seq peaks increasing near the mitochondrial control region. Differentiation of liver organoids resulted in the expression of transcription factors that act as enhancers and repressors. In addition, epigenetic mechanisms regulating the expression of alpha-fetoprotein (AFP) and albumin (ALB) differed in liver organoids and adult liver. Knockdown of PDX1, an essential transcription factor for pancreas development, led to the hepatic maturation of liver organoids through regulation of AFP and ALB expression. This integrative analysis of the transcriptomes and epigenomes of liver organoids at the single-cell level may contribute to a better understanding of the regulatory networks during liver development and the further development of mature in vitro human liver models.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: IScience Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: IScience Año: 2023 Tipo del documento: Article