Cargando…

Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes

Human pluripotent stem cell-derived cardiomyocytes (hPSC-CM) are being investigated as a new source of cardiac cells for drug safety assessment. We developed a novel scalable high content microscopy-based method for the detection of cell death in hPSC-CM that can serve for future predictive in vitro...

Descripción completa

Detalles Bibliográficos
Autores principales: Mioulane, Maxime, Foldes, Gabor, Ali, Nadire N., Schneider, Michael D., Harding, Sian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447146/
https://www.ncbi.nlm.nih.gov/pubmed/22896035
http://dx.doi.org/10.1007/s12265-012-9396-1
_version_ 1782244064256589824
author Mioulane, Maxime
Foldes, Gabor
Ali, Nadire N.
Schneider, Michael D.
Harding, Sian E.
author_facet Mioulane, Maxime
Foldes, Gabor
Ali, Nadire N.
Schneider, Michael D.
Harding, Sian E.
author_sort Mioulane, Maxime
collection PubMed
description Human pluripotent stem cell-derived cardiomyocytes (hPSC-CM) are being investigated as a new source of cardiac cells for drug safety assessment. We developed a novel scalable high content microscopy-based method for the detection of cell death in hPSC-CM that can serve for future predictive in vitro cardio-toxicological screens. Using rat neonatal ventricular cardiomyocytes (RVNC) or hPSC-CM, assays for nuclear remodelling, mitochondrial status, apoptosis and necrosis were designed using a combination of fluorescent dyes and antibodies on an automated microscopy platform. This allowed the observation of a chelerythrine-induced concentration-dependent apoptosis to necrosis switch and time-dependent progression of early apoptotic cells towards a necrotic-like phenotype. Susceptibility of hPSC-CM to chelerythrine-stimulated apoptosis varied with time after differentiation, but at most time points, hPSC-CM were more resistant than RVNC. This simple and scalable humanized high-content assay generates accurate cardiotoxicity profiles that can serve as a base for further assessment of cardioprotective strategies and drug safety. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12265-012-9396-1) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-3447146
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-34471462012-09-27 Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes Mioulane, Maxime Foldes, Gabor Ali, Nadire N. Schneider, Michael D. Harding, Sian E. J Cardiovasc Transl Res Article Human pluripotent stem cell-derived cardiomyocytes (hPSC-CM) are being investigated as a new source of cardiac cells for drug safety assessment. We developed a novel scalable high content microscopy-based method for the detection of cell death in hPSC-CM that can serve for future predictive in vitro cardio-toxicological screens. Using rat neonatal ventricular cardiomyocytes (RVNC) or hPSC-CM, assays for nuclear remodelling, mitochondrial status, apoptosis and necrosis were designed using a combination of fluorescent dyes and antibodies on an automated microscopy platform. This allowed the observation of a chelerythrine-induced concentration-dependent apoptosis to necrosis switch and time-dependent progression of early apoptotic cells towards a necrotic-like phenotype. Susceptibility of hPSC-CM to chelerythrine-stimulated apoptosis varied with time after differentiation, but at most time points, hPSC-CM were more resistant than RVNC. This simple and scalable humanized high-content assay generates accurate cardiotoxicity profiles that can serve as a base for further assessment of cardioprotective strategies and drug safety. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12265-012-9396-1) contains supplementary material, which is available to authorized users. Springer US 2012-08-16 2012 /pmc/articles/PMC3447146/ /pubmed/22896035 http://dx.doi.org/10.1007/s12265-012-9396-1 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Mioulane, Maxime
Foldes, Gabor
Ali, Nadire N.
Schneider, Michael D.
Harding, Sian E.
Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title_full Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title_fullStr Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title_full_unstemmed Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title_short Development of High Content Imaging Methods for Cell Death Detection in Human Pluripotent Stem Cell-Derived Cardiomyocytes
title_sort development of high content imaging methods for cell death detection in human pluripotent stem cell-derived cardiomyocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447146/
https://www.ncbi.nlm.nih.gov/pubmed/22896035
http://dx.doi.org/10.1007/s12265-012-9396-1
work_keys_str_mv AT mioulanemaxime developmentofhighcontentimagingmethodsforcelldeathdetectioninhumanpluripotentstemcellderivedcardiomyocytes
AT foldesgabor developmentofhighcontentimagingmethodsforcelldeathdetectioninhumanpluripotentstemcellderivedcardiomyocytes
AT alinadiren developmentofhighcontentimagingmethodsforcelldeathdetectioninhumanpluripotentstemcellderivedcardiomyocytes
AT schneidermichaeld developmentofhighcontentimagingmethodsforcelldeathdetectioninhumanpluripotentstemcellderivedcardiomyocytes
AT hardingsiane developmentofhighcontentimagingmethodsforcelldeathdetectioninhumanpluripotentstemcellderivedcardiomyocytes