J 2019

Human Embryonic Stem Cells Acquire Responsiveness to TRAIL upon Exposure to Cisplatin

PEŠKOVÁ, Lucie, Vladimír VINARSKÝ, Tomáš BÁRTA a Aleš HAMPL

Základní údaje

Originální název

Human Embryonic Stem Cells Acquire Responsiveness to TRAIL upon Exposure to Cisplatin

Autoři

PEŠKOVÁ, Lucie (203 Česká republika, domácí), Vladimír VINARSKÝ (203 Česká republika, domácí), Tomáš BÁRTA (203 Česká republika, domácí) a Aleš HAMPL (203 Česká republika, garant, domácí)

Vydání

Stem Cells International, London, HINDAWI LTD, 2019, 1687-966X

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10601 Cell biology

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.869

Kód RIV

RIV/00216224:14110/19:00108504

Organizační jednotka

Lékařská fakulta

UT WoS

000482101000001

Klíčová slova anglicky

APOPTOSIS-INDUCING LIGAND; ANTITUMOR-ACTIVITY; CARCINOMA CELLS; DNA; DEATH; DIFFERENTIATION; COMBINATION; ACTIVATION; CASPASE-10; RECEPTORS

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 11. 5. 2020 09:58, Mgr. Tereza Miškechová

Anotace

V originále

Tumor necrosis factor-related apoptosis-inducing ligand-TRAIL-is a protein operating as a ligand capable of inducing apoptosis particularly in cancerously transformed cells, while normal healthy cells are typically nonresponsive. We have previously demonstrated that pluripotent human embryonic stem cells (hESC) are also refractory to TRAIL, even though they express all canonical components of the death receptor-induced apoptosis pathway. In this study, we have examined a capacity of DNA damage to provoke sensitivity of hESC to TRAIL. The extent of DNA damage, behavior of molecules involved in apoptosis, and response of hESC to TRAIL were investigated. The exposure of hESC to 1 mu M and 2 mu M concentrations of cisplatin have led to the formation of 53BP1 and gamma H2AX foci, indicating the presence of double-strand breaks in DNA, without affecting the expression of proteins contributing to mitochondrial membrane integrity. Interestingly, cisplatin upregulated critical components of the extrinsic apoptotic pathway-initiator caspase 8, effector caspase 3, and the cell death receptors. The observed increase of expression of the extrinsic apoptotic pathway components was sufficient to sensitize hESC to TRAIL-induced apoptosis; immense cell dying accompanied by enhanced PARP cleavage, processing of caspase 8, and full activation of caspase 3 were all observed after the treatment combining cisplatin and TRAIL. Finally, we have demonstrated the central role of caspase 8 in this process, since its downregulation abrogated the sensitizing effect of cisplatin.

Návaznosti

NV16-31501A, projekt VaV
Název: Tkáňové inženýrství epitelů: Buňky a protokoly pro regenerativní medicínu