-
Je něco špatně v tomto záznamu ?
Oxygen Is an Ambivalent Factor for the Differentiation of Human Pluripotent Stem Cells in Cardiac 2D Monolayer and 3D Cardiac Spheroids
M. Souidi, Y. Sleiman, I. Acimovic, J. Pribyl, A. Charrabi, V. Baecker, V. Scheuermann, M. Pesl, S. Jelinkova, P. Skladal, P. Dvorak, A. Lacampagne, V. Rotrekl, AC. Meli
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
project 16073
French Muscular Dystrophy Association
20225
AFM-Téléthon
NLK
Directory of Open Access Journals
od 2000
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
33440843
DOI
10.3390/ijms22020662
Knihovny.cz E-zdroje
- MeSH
- biologické markery MeSH
- buněčná diferenciace * MeSH
- buněčné kultury MeSH
- buněčné sféroidy MeSH
- exprese genu MeSH
- kardiomyocyty cytologie metabolismus MeSH
- kyslík metabolismus MeSH
- lidé MeSH
- pluripotentní kmenové buňky cytologie metabolismus MeSH
- sarkoplazmatické retikulum metabolismus MeSH
- srdeční mitochondrie metabolismus MeSH
- vápník metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Numerous protocols of cardiac differentiation have been established by essentially focusing on specific growth factors on human pluripotent stem cell (hPSC) differentiation efficiency. However, the optimal environmental factors to obtain cardiac myocytes in network are still unclear. The mesoderm germ layer differentiation is known to be enhanced by low oxygen exposure. Here, we hypothesized that low oxygen exposure enhances the molecular and functional maturity of the cardiomyocytes. We aimed at comparing the molecular and functional consequences of low (5% O2 or LOE) and high oxygen exposure (21% O2 or HOE) on cardiac differentiation of hPSCs in 2D- and 3D-based protocols. hPSC-CMs were differentiated through both the 2D (monolayer) and 3D (embryoid body) protocols using several lines. Cardiac marker expression and cell morphology were assessed. The mitochondrial localization and metabolic properties were evaluated. The intracellular Ca2+ handling and contractile properties were also monitored. The 2D cardiac monolayer can only be differentiated in HOE. The 3D cardiac spheroids containing hPSC-CMs in LOE further exhibited cardiac markers, hypertrophy, steadier SR Ca2+ release properties revealing a better SR Ca2+ handling, and enhanced contractile force. Preserved distribution of mitochondria and similar oxygen consumption by the mitochondrial respiratory chain complexes were also observed. Our results brought evidences that LOE is moderately beneficial for the 3D cardiac spheroids with hPSC-CMs exhibiting further maturity. In contrast, the 2D cardiac monolayers strictly require HOE.
CEITEC Masaryk University 62500 Brno Czech Republic
Department of Biology Faculty of Medicine Masaryk University 62500 Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno 65691 Brno Czech Republic
PhyMedExp INSERM University of Montpellier CNRS 34000 Montpellier France
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019458
- 003
- CZ-PrNML
- 005
- 20240305152653.0
- 007
- ta
- 008
- 210728s2021 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms22020662 $2 doi
- 035 __
- $a (PubMed)33440843
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Souidi, Monia $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 245 10
- $a Oxygen Is an Ambivalent Factor for the Differentiation of Human Pluripotent Stem Cells in Cardiac 2D Monolayer and 3D Cardiac Spheroids / $c M. Souidi, Y. Sleiman, I. Acimovic, J. Pribyl, A. Charrabi, V. Baecker, V. Scheuermann, M. Pesl, S. Jelinkova, P. Skladal, P. Dvorak, A. Lacampagne, V. Rotrekl, AC. Meli
- 520 9_
- $a Numerous protocols of cardiac differentiation have been established by essentially focusing on specific growth factors on human pluripotent stem cell (hPSC) differentiation efficiency. However, the optimal environmental factors to obtain cardiac myocytes in network are still unclear. The mesoderm germ layer differentiation is known to be enhanced by low oxygen exposure. Here, we hypothesized that low oxygen exposure enhances the molecular and functional maturity of the cardiomyocytes. We aimed at comparing the molecular and functional consequences of low (5% O2 or LOE) and high oxygen exposure (21% O2 or HOE) on cardiac differentiation of hPSCs in 2D- and 3D-based protocols. hPSC-CMs were differentiated through both the 2D (monolayer) and 3D (embryoid body) protocols using several lines. Cardiac marker expression and cell morphology were assessed. The mitochondrial localization and metabolic properties were evaluated. The intracellular Ca2+ handling and contractile properties were also monitored. The 2D cardiac monolayer can only be differentiated in HOE. The 3D cardiac spheroids containing hPSC-CMs in LOE further exhibited cardiac markers, hypertrophy, steadier SR Ca2+ release properties revealing a better SR Ca2+ handling, and enhanced contractile force. Preserved distribution of mitochondria and similar oxygen consumption by the mitochondrial respiratory chain complexes were also observed. Our results brought evidences that LOE is moderately beneficial for the 3D cardiac spheroids with hPSC-CMs exhibiting further maturity. In contrast, the 2D cardiac monolayers strictly require HOE.
- 650 _2
- $a biologické markery $7 D015415
- 650 _2
- $a vápník $x metabolismus $7 D002118
- 650 _2
- $a buněčné kultury $7 D018929
- 650 12
- $a buněčná diferenciace $7 D002454
- 650 _2
- $a exprese genu $7 D015870
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a srdeční mitochondrie $x metabolismus $7 D008929
- 650 _2
- $a kardiomyocyty $x cytologie $x metabolismus $7 D032383
- 650 _2
- $a kyslík $x metabolismus $7 D010100
- 650 _2
- $a pluripotentní kmenové buňky $x cytologie $x metabolismus $7 D039904
- 650 _2
- $a sarkoplazmatické retikulum $x metabolismus $7 D012519
- 650 _2
- $a buněčné sféroidy $7 D018874
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Sleiman, Yvonne $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 700 1_
- $a Aćimović, Ivana $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France $u Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic $7 xx0314769
- 700 1_
- $a Pribyl, Jan $u CEITEC, Masaryk University, 62500 Brno, Czech Republic
- 700 1_
- $a Charrabi, Azzouz $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 700 1_
- $a Baecker, Volker $u Montpellier Ressources Imagerie, BioCampus Montpellier, CNRS, INSERM, University of Montpellier, 34000 Montpellier, France
- 700 1_
- $a Scheuermann, Valerie $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 700 1_
- $a Pesl, Martin $u Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic $u International Clinical Research Center, St. Anne's University Hospital Brno, 65691 Brno, Czech Republic $u First Department of Internal Medicine/Cardioangiology, St. Anne's Hospital, Masaryk University, 65691 Brno, Czech Republic
- 700 1_
- $a Jelinkova, Sarka $u Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic
- 700 1_
- $a Skladal, Petr $u CEITEC, Masaryk University, 62500 Brno, Czech Republic
- 700 1_
- $a Dvorak, Petr $u Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic
- 700 1_
- $a Lacampagne, Alain $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 700 1_
- $a Rotrekl, Vladimir $u Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic $u International Clinical Research Center, St. Anne's University Hospital Brno, 65691 Brno, Czech Republic
- 700 1_
- $a Meli, Albano C $u PhyMedExp, INSERM, University of Montpellier, CNRS, 34000 Montpellier, France
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 22, č. 2 (2021)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33440843 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20240305152649 $b ABA008
- 999 __
- $a ok $b bmc $g 1690308 $s 1139904
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 22 $c 2 $e 20210111 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a project 16073 $p French Muscular Dystrophy Association
- GRA __
- $a 20225 $p AFM-Téléthon
- LZP __
- $a Pubmed-20210728