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Sökning: L773:1531 2267 OR L773:1094 8341 > (2015-2019) > Comparative transcr...

Comparative transcriptomics of hepatic differentiation of human pluripotent stem cells and adult human liver tissue

Ghosheh, Nidal (författare)
Högskolan i Skövde,Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine,Forskningscentrum för Systembiologi,Institutionen för biovetenskap,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden,Bioinformatik, Bioinformatics
Kuppers-Munther, B. (författare)
Takara Bio Europe Aktiebolaget, Gothenburg, Sweden
Asplund, A. (författare)
Takara Bio Europe Aktiebolaget, Gothenburg, Sweden
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Edsbagge, J. (författare)
Takara Bio Europe Aktiebolaget, Gothenburg, Sweden
Ulfenborg, Benjamin (författare)
Högskolan i Skövde,Institutionen för biovetenskap,Forskningscentrum för Systembiologi,Bioinformatik, Bioinformatics
Andersson, T. B. (författare)
Cardiovascular and Metabolic Diseases, Innovative Medicines and Early Development Biotech Unit, AstraZeneca, Mölndal, Sweden / Department of Physiology and Pharmacology, Section of Pharmacogenetics, Karolinska Institutet, Stockholm, Sweden
Bjorquist, P. (författare)
NovaHep Aktiebolaget, Gothenburg, Sweden
Andersson, C. X. (författare)
Takara Bio Europe Aktiebolaget, Gothenburg, Sweden
Carén, Helena, 1979 (författare)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology,Sahlgrenska Cancer Center, Department of Pathology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
Simonsson, Stina, 1969 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
Sartipy, Peter (författare)
Högskolan i Skövde,Institutionen för biovetenskap,Forskningscentrum för Systembiologi,AstraZeneca Research and Development, Global Medicines Development Cardiovascular and Metabolic Diseases Global Medicines Development Unit, Mölndal, Sweden,Bioinformatik, Bioinformatics
Synnergren, Jane (författare)
Högskolan i Skövde,Institutionen för biovetenskap,Forskningscentrum för Systembiologi,Bioinformatik, Bioinformatics
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 (creator_code:org_t)
American Physiological Society, 2017
2017
Engelska.
Ingår i: Physiological Genomics. - : American Physiological Society. - 1094-8341 .- 1531-2267. ; 49:8, s. 430-446
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Hepatocytes derived from human pluripotent stem cells (hPSC-HEP) have the potential to replace presently used hepatocyte sources applied in liver disease treatment and models of drug discovery and development. Established hepatocyte differentiation protocols are effective and generate hepatocytes, which recapitulate some key features of their in vivo counterparts. However, generating mature hPSC-HEP remains a challenge. In this study, we applied transcriptomics to investigate the progress of in vitro hepatic differentiation of hPSCs at the developmental stages, definitive endoderm, hepatoblasts, early hPSC-HEP, and mature hPSC-HEP, to identify functional targets that enhance efficient hepatocyte differentiation. Using functional annotation, pathway and protein interaction network analyses, we observed the grouping of differentially expressed genes in specific clusters representing typical developmental stages of hepatic differentiation. In addition, we identified hub proteins and modules that were involved in the cell cycle process at early differentiation stages. We also identified hub proteins that differed in expression levels between hPSC-HEP and the liver tissue controls. Moreover, we identified a module of genes that were expressed at higher levels in the liver tissue samples than in the hPSC-HEP. Considering that hub proteins and modules generally are essential and have important roles in the protein-protein interactions, further investigation of these genes and their regulators may contribute to a better understanding of the differentiation process. This may suggest novel target pathways and molecules for improvement of hPSC-HEP functionality, having the potential to finally bring this technology to a wider use.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Nyckelord

human pluripotent stem cell
stem cell-derived hepatocytes
liver tissue
differentiation
HEPATOCYTE-LIKE CELLS
GENE-EXPRESSION
BIOLOGICAL NETWORKS
MODELS
METABOLISM
CHALLENGES
PATHWAY
INJURY
LEVEL
FETAL
human pluripotent stem cell
Bioinformatik
INF501 Integration of -omics Data
INF502 Biomarkers

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