VEČEŘA, Josef, Jana KUDOVÁ, Jan KUČERA, Lukáš KUBALA and Jiří PACHERNÍK. Neural Differentiation Is Inhibited through HIF1 alpha/ beta-Catenin Signaling in Embryoid Bodies. Stem Cells International. London: HINDAWI LTD, 2017, Neuveden, prosinec, p. nestránkováno, 12 pp. ISSN 1687-966X. Available from: https://dx.doi.org/10.1155/2017/8715798.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Neural Differentiation Is Inhibited through HIF1 alpha/ beta-Catenin Signaling in Embryoid Bodies
Authors VEČEŘA, Josef (203 Czech Republic, guarantor, belonging to the institution), Jana KUDOVÁ (203 Czech Republic), Jan KUČERA (203 Czech Republic, belonging to the institution), Lukáš KUBALA (203 Czech Republic, belonging to the institution) and Jiří PACHERNÍK (203 Czech Republic, belonging to the institution).
Edition Stem Cells International, London, HINDAWI LTD, 2017, 1687-966X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10605 Developmental biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.989
RIV identification code RIV/00216224:14310/17:00095557
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1155/2017/8715798
UT WoS 000419057500001
Keywords in English STEM-CELL FATE; HYPOXIA; OXYGEN; HIF; CATENIN
Tags NZ, rivok
Changed by Changed by: Ing. Nicole Zrilić, učo 240776. Changed: 9/4/2018 15:50.
Abstract
Extensive research in the field of stem cells and developmental biology has revealed evidence of the role of hypoxia as an important factor regulating self-renewal and differentiation. However, comprehensive information about the exact hypoxia-mediated regulatory mechanism of stem cell fate during early embryonic development is still missing. Using a model of embryoid bodies (EBs) derived from murine embryonic stem cells (ESC), we here tried to encrypt the role of hypoxia-inducible factor 1 alpha (HIF1 alpha) in neural fate during spontaneous differentiation. EBs derived from ESC with the ablated gene for HIF1a had abnormally increased neuronal characteristics during differentiation. An increased neural phenotype in Hif1 alpha(-/-) EBs was accompanied by the disruption of beta-catenin signaling together with the increased cytoplasmic degradation of beta-catenin. The knock-in of Hif1 alpha, as well as beta-catenin ectopic overexpression in Hif1 alpha(-/-) EBs, induced a reduction in neural markers to the levels observed in wild-type EBs. Interestingly, direct interaction between HIF1 alpha and beta-catenin was demonstrated by immunoprecipitation analysis of the nuclear fraction of wild-type EBs. Together, these results emphasize the regulatory role of HIF1 alpha in beta-catenin stabilization during spontaneous differentiation, which seems to be a crucial mechanism for the natural inhibition of premature neural differentiation.
Links
GJ15-13443Y, research and development projectName: Úloha hypoxií indukovaného faktoru 1 alfa ve vývoji populace neurálních kmenových buněk myši
Investor: Czech Science Foundation
PrintDisplayed: 21/7/2024 12:19