OMELYANENKO, Anna, Petra SEKYROVÁ a Michael ANDÄNG. ZD7288, a blocker of the HCN channel family, increases doubling time of mouse embryonic stem cells and modulates differentiation outcomes in a context-dependent manner. SpringerPlus. Cham: Springer International Publishing, 2016, roč. 5, January, s. nestránkováno, 10 s. ISSN 2193-1801. Dostupné z: https://dx.doi.org/10.1186/s40064-016-1678-7.
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Základní údaje
Originální název ZD7288, a blocker of the HCN channel family, increases doubling time of mouse embryonic stem cells and modulates differentiation outcomes in a context-dependent manner
Autoři OMELYANENKO, Anna (752 Švédsko), Petra SEKYROVÁ (203 Česká republika, domácí) a Michael ANDÄNG (752 Švédsko, garant, domácí).
Vydání SpringerPlus, Cham, Springer International Publishing, 2016, 2193-1801.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10600 1.6 Biological sciences
Stát vydavatele Švýcarsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 1.130
Kód RIV RIV/00216224:14740/16:00088770
Organizační jednotka Středoevropský technologický institut
Doi http://dx.doi.org/10.1186/s40064-016-1678-7
UT WoS 000368875900004
Klíčová slova anglicky Embryonic stem cells; Ion channel modulator; ZD7288; Differentiation; Proliferation; Pluripotency; Cell cycle; Serum
Štítky rivok
Změnil Změnila: Mgr. Pavla Foltynová, Ph.D., učo 106624. Změněno: 5. 3. 2018 15:56.
Anotace
Pluripotent stem cells are the starting cell type of choice for the development of many cell-based regenerative therapies due to their rapid and unlimited proliferation and broad differentiation potential. The unique pluripotent cell cycle underlies both these properties. Hyperpolarization-activated cyclic nucleotide-gated cation (HCN) family channels have previously been reported to modulate mouse embryonic stem cell (ESC) proliferation and here we characterize the effects of HCN inhibitor ZD7288 on ESC proliferation and stem cell identity. The doubling time of cells treated with the HCN blocker increased by similar to 30 % due to longer G1 and S phases, resulting in a nearly twofold reduction in ESC numbers after 4 day serum-free culture. Slower progression through S phase was not accompanied by H2AX phosphorylation or cell stalling at transition points, although EdU incorporation in treated cells was reduced. Despite the drastic cell cycle perturbations, the pluripotent status of the cells was not compromised by treatment. Cultures treated with the HCN blocker in maintenance conditions maintained pluripotency marker expression on both RNA and protein level, although we observed a reversible effect on morphology and colony formation frequency. Addition of ZD7288 in differentiating media improved FBS-driven differentiation, but not directed differentiation to neuroectoderm, further indicating that altered cell cycle structure does not necessarily compromise pluripotency and drive ESCs to differentiation. The categorically different outcomes of ZD7288 use during differentiation indicate that cell culture context can be determinative for effects of ion-modulatory molecules and underscores the need for exploring their action in serum-free conditions demanded by potential clinical use.
Návaznosti
GA15-20818S, projekt VaVNázev: Cílená terapie proti rezistentím kmenovým buňkám gliomového nádoru - kontrola přísunu živin pomocí iontových kanálů
Investor: Grantová agentura ČR, Cílená terapie proti rezistentím kmenovým buňkám gliomového nádoru - kontrola přísunu živin pomocí iontových kanálů
VytisknoutZobrazeno: 10. 9. 2024 11:41