| Literature DB >> 28370937 |
Houda Montacir1,2, Nora Freyer3, Fanny Knöspel3, Thomas Urbaniak3, Tereza Dedova1,2, Markus Berger1, Georg Damm4,5, Rudolf Tauber1, Katrin Zeilinger3, Véronique Blanchard1.
Abstract
Human embryonic stem cells (hESCs) are pluripotent stem cells that offer a wide range of applications in regenerative medicine. In addition, they have been proposed as an appropriate alternative source of hepatocytes. In this work, hESCs were differentiated into definitive endodermal cells (DECs), followed by maturation into hepatocyte-like cells (HLCs). Their cell-surface N-glycome was profiled and also compared with that of primary human hepatocytes (PHHs). Undifferentiated hESCs contained large amounts of high-mannose N-glycans. In contrast, complex-type N-glycans such as asialylated or monosialylated biantennary and triantennary N-glycans were dominant in HLCs, and fully galactosylated structures were significantly more abundant than in undifferentiated hESCs. The cell-surface N-glycosylation of PHHs was more biologically processed than that of HLCs, with bisialylated biantennary and trisialylated triantennary structures predominant. This is the first report of the cell surface N-glycome of PHHs and of HLCs being directly generated from hESCs without embryoid body formation.Entities:
Keywords: N-glycans; carbohydrates; glycosylation; hepatocytes; human embryonic stem cells
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Year: 2017 PMID: 28370937 DOI: 10.1002/cbic.201700001
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164