FEDOROVÁ, Veronika, Tereza VÁŇOVÁ, Lina Mohamed Bahaael ELREFAE, Jakub POSPÍŠIL, Martina PETRÁŠOVÁ, Veronika KOLAJOVÁ, Zuzana HUDACOVA, Jana BANIARIOVÁ, Martin BARÁK, Lucie PEŠKOVÁ, Tomáš BÁRTA, Markéta KAUCKÁ, Michael KILLINGER, Josef VEČEŘA, Ondřej BERNATÍK, Lukáš ČAJÁNEK, Hana HŘÍBKOVÁ and Dáša BOHAČIAKOVÁ. Differentiation of neural rosettes from human pluripotent stem cells in vitro is sequentially regulated on a molecular level and accomplished by the mechanism reminiscent of secondary neurulation. Stem Cell Research. Amsterdam: Elsevier Science BV, 2019, vol. 40, OCT 2019, p. 1-10. ISSN 1873-5061. Available from: https://dx.doi.org/10.1016/j.scr.2019.101563.
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Basic information
Original name Differentiation of neural rosettes from human pluripotent stem cells in vitro is sequentially regulated on a molecular level and accomplished by the mechanism reminiscent of secondary neurulation
Authors FEDOROVÁ, Veronika (203 Czech Republic, belonging to the institution), Tereza VÁŇOVÁ (203 Czech Republic, belonging to the institution), Lina Mohamed Bahaael ELREFAE (818 Egypt, belonging to the institution), Jakub POSPÍŠIL (203 Czech Republic, belonging to the institution), Martina PETRÁŠOVÁ (703 Slovakia, belonging to the institution), Veronika KOLAJOVÁ (203 Czech Republic, belonging to the institution), Zuzana HUDACOVA (203 Czech Republic), Jana BANIARIOVÁ (703 Slovakia, belonging to the institution), Martin BARÁK (203 Czech Republic, belonging to the institution), Lucie PEŠKOVÁ (203 Czech Republic, belonging to the institution), Tomáš BÁRTA (203 Czech Republic, belonging to the institution), Markéta KAUCKÁ (203 Czech Republic), Michael KILLINGER (203 Czech Republic), Josef VEČEŘA (203 Czech Republic, belonging to the institution), Ondřej BERNATÍK (203 Czech Republic, belonging to the institution), Lukáš ČAJÁNEK (203 Czech Republic, belonging to the institution), Hana HŘÍBKOVÁ (203 Czech Republic, belonging to the institution) and Dáša BOHAČIAKOVÁ (703 Slovakia, guarantor, belonging to the institution).
Edition Stem Cell Research, Amsterdam, Elsevier Science BV, 2019, 1873-5061.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.495
RIV identification code RIV/00216224:14110/19:00107663
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.scr.2019.101563
UT WoS 000491224500006
Keywords in English BMP; Differentiation; Human embryonic stem cells; Induced pluripotent stem cells; Neural rosettes; Secondary neurulation
Tags 14110517, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 22/6/2020 07:52.
Abstract
Development of neural tube has been extensively modeled in vitro using human pluripotent stem cells (hPSCs) that are able to form radially organized cellular structures called neural rosettes. While a great amount of research has been done using neural rosettes, studies have only inadequately addressed how rosettes are formed and what the molecular mechanisms and pathways involved in their formation are. Here we address this question by detailed analysis of the expression of pluripotency and differentiation-associated proteins during the early onset of differentiation of hPSCs towards neural rosettes. Additionally, we show that the BMP signaling is likely contributing to the formation of the complex cluster of neural rosettes and its inhibition leads to the altered expression of PAX6, SOX2 and SOX1 proteins and the rosette morphology. Finally, we provide evidence that the mechanism of neural rosettes formation in vitro is reminiscent of the process of secondary neurulation rather than that of primary neurulation in vivo. Since secondary neurulation is a largely unexplored process, its understanding will ultimately assist the development of methods to prevent caudal neural tube defects in humans.
Links
GA19-05244S, research and development projectName: Molekulární aspekty ciliogeneze: zaměření na Tau Tubulin Kinázu 2
Investor: Czech Science Foundation
GJ15-13443Y, research and development projectName: Úloha hypoxií indukovaného faktoru 1 alfa ve vývoji populace neurálních kmenových buněk myši
Investor: Czech Science Foundation
GJ15-18316Y, research and development projectName: Úloha microRNA v řízení buněčného dělení a diferenciace lidských embryonálních kmenových buněk do neurálních kmenových buněk. (Acronym: miRNA v diferenciaci lidských EK buněk)
Investor: Czech Science Foundation
GJ16-03269Y, research and development projectName: Tau tubulin kináza 2 v ciliogenezi: molekulární mechanismy a funkční důsledky
Investor: Czech Science Foundation
GJ16-24004Y, research and development projectName: Indukce buněčné plasticity prostřednictvím modulace mikroRNA molekul: Nový přístup pro přeprogramování buněk
Investor: Czech Science Foundation
GJ18-25429Y, research and development projectName: Funkční studie mikroRNA u nerálních kmenových buněk v průběhu diferenciace
Investor: Czech Science Foundation
IZ11Z0_166533/1, interní kód MUName: Tau tubulin kinase 2 in ciliogenesis: mechanisms and functions
Investor: Ostatní - foreign, Promotion of Young Scientists in Eastern Europe (PROMYS)
MUNI/A/1565/2018, interní kód MUName: Zdroje pro tkáňové inženýrství 9 (Acronym: TissueEng 9)
Investor: Masaryk University, Category A
MUNI/C/1434/2017, interní kód MUName: Investigating the Role of p53 in Neural Differentiation Using Cerebral Organoids
Investor: Masaryk University, Rector's Program
MUNI/C/1436/2017, interní kód MUName: Role proteinu p16/INK4A v biologii lidských embryonálních kmenových buněk
Investor: Masaryk University, Rector's Program
ROZV/24/LF/2018, interní kód MUName: LF - Příspěvek na IP 2108
Investor: Ministry of Education, Youth and Sports of the CR, Internal development projects
ROZV/25/LF/2017, interní kód MUName: LF - Příspěvek na IP 2017
Investor: Ministry of Education, Youth and Sports of the CR, Internal development projects
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