2019
Simultaneous study of mechanobiology and calcium dynamics on hESC-derived cardiomyocytes clusters
CALUORI, Guido, Jan PŘIBYL, Vratislav CMIEL, Martin PEŠL, Tomas POTOCNAK et. al.Základní údaje
Originální název
Simultaneous study of mechanobiology and calcium dynamics on hESC-derived cardiomyocytes clusters
Autoři
CALUORI, Guido (380 Itálie, domácí), Jan PŘIBYL (203 Česká republika, garant, domácí), Vratislav CMIEL (203 Česká republika), Martin PEŠL (203 Česká republika, domácí), Tomas POTOCNAK (203 Česká republika), Ivo PROVAZNÍK (203 Česká republika), Petr SKLÁDAL (203 Česká republika, domácí) a Vladimír ROTREKL (203 Česká republika, domácí)
Vydání
Journal of Molecular Recognition, Hoboken, Wiley, 2019, 0952-3499
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.214
Kód RIV
RIV/00216224:14740/19:00107155
Organizační jednotka
Středoevropský technologický institut
UT WoS
000459589700001
Klíčová slova anglicky
calcium imaging; atomic force microscopy; human stem cell-derived cardiomyocytes; in vitro models; fluorescence microscopy; cardiac differentiation; caffeine; embryoid bodies; biosignals filtering
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 10. 2024 11:51, Mgr. Adéla Pešková
Anotace
V originále
Calcium ions act like ubiquitous second messengers in a wide amount of cellular processes. In cardiac myocytes, Ca2+ handling regulates the mechanical contraction necessary to the heart pump function. The field of intracellular and intercellular Ca2+ handling, employing in vitro models of cardiomyocytes, has become a cornerstone to understand the role and adaptation of calcium signalling in healthy and diseased hearts. Comprehensive in vitro systems and cell-based biosensors are powerful tools to enrich and speed up cardiac phenotypic and drug response evaluation. We have implemented a combined setup to measure contractility and calcium waves in human embryonic stem cells-derived cardiomyocyte 3D clusters, obtained from embryoid body differentiation. A combination of atomic force microscopy to monitor cardiac contractility, and sensitive fast scientific complementary metal-oxide-semiconductor camera for epifluorescence video recording, provided correlated signals in real time. To speed up the integrated data processing, we tested several post-processing algorithms, to improve the automatic detection of relevant functional parameters. The validation of our proposed method was assessed by caffeine stimulation (10mM) and detection/characterization of the induced cardiac response. We successfully report the first simultaneous recording of cardiac contractility and calcium waves on the described cardiac 3D models. The drug stimulation confirmed the automatic detection capabilities of the used algorithms, measuring expected physiological response, such as elongation of contraction time and Ca2+ cytosolic persistence, increased calcium basal fluorescence, and transient peaks. These results contribute to the implementation of novel, integrated, high-information, and reliable experimental systems for cardiac models and drug evaluation.
Návaznosti
GA18-24089S, projekt VaV |
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LM2015043, projekt VaV |
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LQ1601, projekt VaV |
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MUNI/A/1087/2018, interní kód MU |
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