Generation of glycogen- and albumin-producing hepatocyte-like cells from embryonic stem cells

Verfasser / Beitragende:
[Gabriela Kania, Przemyslaw Blyszczuk, Andrea Jochheim, Michael Ott, Anna M. Wobus]
Ort, Verlag, Jahr:
2004
Enthalten in:
Biological Chemistry, 385/10(2004-10-01), 943-953
Format:
Artikel (online)
ID: 378941070
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024 7 0 |a 10.1515/BC.2004.123  |2 doi 
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245 0 0 |a Generation of glycogen- and albumin-producing hepatocyte-like cells from embryonic stem cells  |h [Elektronische Daten]  |c [Gabriela Kania, Przemyslaw Blyszczuk, Andrea Jochheim, Michael Ott, Anna M. Wobus] 
520 3 |a We present a novel two-step protocol for the differentiation of embryonic stem (ES) cells into the hepatic lineage. Differentiated hepatocyte-like cells express genes and proteins characteristic for endodermal and hepatic cells and acquire a functional hepatic phenotype as demonstrated by albumin secretion and glycogen storage. During differentiation, α-fetoprotein, albumin, transthyretin, α-1-antitrypsin, cytochrome P450 subunits 2b9 and 2b13 and tyrosine aminotransferase transcripts are upregulated. Quantitative RT-PCR data revealed a fetal hepatic phenotype corresponding to day 13-14 of liver development. Terminally differentiated hepatocyte-like cells show a bi-nucleated, cuboidal morphology labeled by albumin, α-1-antitrypsin, liver amylase, dipeptidyl peptidase IV, c-met and cytokeratin 18. ES-derived intermediate cell types transiently and partially co-express nestin with albumin and α-fetoprotein, respectively, but not cytokeratin 19. This finding suggests an ES-derived potential hepatic progenitor cell type, which is partially nestin-, albumin- and α-fetoproteinpositive, but cytokeratin 19-negative. 
540 |a © Walter de Gruyter 
690 7 |a Biochemistry  |2 nationallicence 
690 7 |a Molecular biology  |2 nationallicence 
690 7 |a Cellular biology  |2 nationallicence 
690 7 |a albumin  |2 nationallicence 
690 7 |a α-fetoprotein  |2 nationallicence 
690 7 |a embryonic stem cells  |2 nationallicence 
690 7 |a hepatic differentiation  |2 nationallicence 
690 7 |a mouse  |2 nationallicence 
690 7 |a nestin  |2 nationallicence 
700 1 |a Kania  |D Gabriela  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
700 1 |a Blyszczuk  |D Przemyslaw  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
700 1 |a Jochheim  |D Andrea  |u Hannover Medical School, Center of Internal Medicine, Department of Gastroenterology, Hepatology and Endocrinology, D-30625 Hannover, Germany  |4 aut 
700 1 |a Ott  |D Michael  |u Hannover Medical School, Center of Internal Medicine, Department of Gastroenterology, Hepatology and Endocrinology, D-30625 Hannover, Germany  |4 aut 
700 1 |a Wobus  |D Anna M.  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
773 0 |t Biological Chemistry  |d Walter de Gruyter  |g 385/10(2004-10-01), 943-953  |x 1431-6730  |q 385:10<943  |1 2004  |2 385  |o bchm 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kania  |D Gabriela  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Blyszczuk  |D Przemyslaw  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jochheim  |D Andrea  |u Hannover Medical School, Center of Internal Medicine, Department of Gastroenterology, Hepatology and Endocrinology, D-30625 Hannover, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ott  |D Michael  |u Hannover Medical School, Center of Internal Medicine, Department of Gastroenterology, Hepatology and Endocrinology, D-30625 Hannover, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Wobus  |D Anna M.  |u In vitro Differentiation Group, IPK Gatersleben, D-06466 Gatersleben, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Biological Chemistry  |d Walter de Gruyter  |g 385/10(2004-10-01), 943-953  |x 1431-6730  |q 385:10<943  |1 2004  |2 385  |o bchm 
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