Non-invasive electromechanical cell-based biosensors for improved investigation of 3D cardiac models
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
30366257
DOI
10.1016/j.bios.2018.10.021
PII: S0956-5663(18)30831-5
Knihovny.cz E-zdroje
- Klíčová slova
- Atomic force microscopy, Cardiomyocytes, Drug testing, Excitation-contraction coupling, Human pluripotent stem cells, Microelectrode array,
- MeSH
- biosenzitivní techniky * MeSH
- buněčná diferenciace genetika MeSH
- Duchennova muskulární dystrofie patofyziologie MeSH
- dystrofin genetika MeSH
- fibroblasty účinky léků ultrastruktura MeSH
- indukované pluripotentní kmenové buňky metabolismus ultrastruktura MeSH
- isoprenalin farmakologie MeSH
- kardiomyocyty cytologie MeSH
- kontrakce myokardu genetika fyziologie MeSH
- lidé MeSH
- mikroelektrody MeSH
- mikroskopie atomárních sil MeSH
- verapamil farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- dystrofin MeSH
- isoprenalin MeSH
- verapamil MeSH
Cardiomyocytes (CM) placed on microelectrode array (MEA) were simultaneously probed with cantilever from atomic force microscope (AFM) system. This electric / nanomechanical combination in real time recorded beating force of the CMs cluster and the triggering electric events. Such "organ-on-a-chip" represents a tool for drug development and disease modeling. The human pluripotent stem cells included the WT embryonic line CCTL14 and the induced dystrophin deficient line reprogrammed from fibroblasts of a patient affected by Duchenne Muscular Dystrophy (DMD, complete loss of dystrophin expression). Both were differentiated to CMs and employed with the AFM/MEA platform for diseased CMs' drug response testing and DMD characterization. The dependence of cardiac parameters on extracellular Ca2+ was studied. The differential evaluation explained the observed effects despite variability of biological samples. The β-adrenergic stimulation (isoproterenol) and antagonist trials (verapamil) addressed ionotropic and chronotropic cell line-dependent features. For the first time, a distinctive beating-force relation for DMD CMs was measured on the 3D cardiac in vitro model.
Central European Institute of Technology Masaryk University Kamenice 5 62500 Brno Czech Republic
Department of Biology Faculty of Medicine Masaryk University Kamenice 5 62500 Brno Czech Republic
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