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Verfasst von:Marinovic, Iva [VerfasserIn]   i
 Bartosova, Maria [VerfasserIn]   i
 Herzog, Rebecca [VerfasserIn]   i
 Sacnun, Juan Manuel [VerfasserIn]   i
 Zhang, Conghui [VerfasserIn]   i
 Hoogenboom, Robin [VerfasserIn]   i
 Unterwurzacher, Markus [VerfasserIn]   i
 Hackert, Thilo [VerfasserIn]   i
 Teleman, Aurelio A. [VerfasserIn]   i
 Kratochwill, Klaus [VerfasserIn]   i
 Schmitt, Claus P. [VerfasserIn]   i
Titel:Understanding cell model characteristics - RNA expression profiling in primary and immortalized human mesothelial cells, and in human vein and microvascular endothelial cells
Verf.angabe:Iva Marinovic, Maria Bartosova, Rebecca Herzog, Juan Manuel Sacnun, Conghui Zhang, Robin Hoogenboom, Markus Unterwurzacher, Thilo Hackert, Aurelio A. Teleman, Klaus Kratochwill and Claus Peter Schmitt
E-Jahr:2022
Jahr:5 October 2022
Umfang:14 S.
Fussnoten:Gesehen am 16.01.2023
Titel Quelle:Enthalten in: Cells
Ort Quelle:Basel : MDPI, 2012
Jahr Quelle:2022
Band/Heft Quelle:11(2022), 19, Artikel-ID 3133, Seite 1-14
ISSN Quelle:2073-4409
Abstract:In vitro studies are essential in pre-clinical research. While choice of cell lines is often driven by handling and cost-effectiveness, in-depth knowledge on specific characteristics is scant. Mesothelial cells, which interact with endothelial cells, are widely used in research, including cancer and drug development, but have not been comprehensively profiled. We therefore performed RNA sequencing of polarized, primary peritoneal (HPMC) and immortalized pleural mesothelial cells (MeT-5A), and compared them to endothelial cells from umbilical vein (HUVEC) and cardiac capillaries (HCMEC). Seventy-seven per cent of 12,760 genes were shared between the 4 cell lines, 1003 were mesothelial and 969 were endothelial cell specific. The transcripts reflected major differences between HPMC and MeT-5A in DNA-related processes, extracellular matrix, migration, proliferation, adhesion, transport, growth factor- and immune response, and between HUVEC and HCMEC in DNA replication, extracellular matrix and adhesion organization. Highly variable shared genes were related to six clusters, cell tissue origin and immortalization, but also cell migration capacity, cell adhesion, regulation of angiogenesis and response to hypoxia. Distinct, cell type specific biological processes were further described by cellular component-, molecular function- and Reactome pathway analyses. We provide crucial information on specific features of the most frequently used mesothelial and endothelial cell lines, essential for appropriate use.
DOI:doi:10.3390/cells11193133
URL:Volltext: https://doi.org/10.3390/cells11193133
 Volltext: https://www.mdpi.com/2073-4409/11/19/3133
 DOI: https://doi.org/10.3390/cells11193133
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:cell models
 endothelium
 in vitro
 mesothelium
 RNA sequencing
K10plus-PPN:1831153238
Verknüpfungen:→ Zeitschrift
 
 
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