2019
Novel synergistic culturing approach for efficient and robust differentiation of human pluripotent stem cells into endothelial progenitors.
FARKAŠ, Šimon, Pavel ŠIMARA, Daniela ŘEHÁKOVÁ, Tereza SOURALOVÁ, Irena KOUTNÁ et. al.Základní údaje
Originální název
Novel synergistic culturing approach for efficient and robust differentiation of human pluripotent stem cells into endothelial progenitors.
Autoři
FARKAŠ, Šimon (703 Slovensko, domácí), Pavel ŠIMARA (203 Česká republika, garant, domácí), Daniela ŘEHÁKOVÁ (203 Česká republika, domácí), Tereza SOURALOVÁ (203 Česká republika, domácí) a Irena KOUTNÁ (203 Česká republika, domácí)
Vydání
8. ročník konference Stem Cells and Cell Therapy: From Research to Modern Clinical Applications, Lednice, Czech Republic, 2019
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10601 Cell biology
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/19:00108561
Organizační jednotka
Lékařská fakulta
Klíčová slova česky
pluripotentní kmenové buňky; endotheliální diferenciace
Klíčová slova anglicky
pluripotent stem cells; endothelial differentiation
Štítky
Změněno: 31. 5. 2023 12:56, Mgr. Tereza Souralová
Anotace
V originále
Cellular therapy is a powerful tool for treating various human diseases and reparation of the damaged vasculature is a specialized subtype of this therapy. Using human pluripotent stem cells (hPSCs) as a starting material, it should be possible to generate high amounts of endothelial progenitor cells (EPCs). Our aim was to develop highly efficient, robust and easily reproducible differentiation protocol that would allow us to produce these high amounts of EPCs. Presented protocol follows proper physiological pathway by differentiating hPSCs in three phases through primitive streak and kinase insert domain receptor (KDR) positive mesoderm into EPCs. The differentiation protocol only takes 5 days and results in high amounts of pure EPCs. The robustness is demonstrated by using both human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Better efficiency and lesser line-to-line variability were observed for our differentiation protocol in comparison to other published protocols. Furthermore, derived EPCs expressed high proliferative potential EPC marker CD157 on their surface in addition to standard EPC markers CD31, CD144, CD34, KDR and C-X-C chemokine receptor type 4 (CXCR4).
Návaznosti
NV16-31501A, projekt VaV |
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