Cargando…

Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy

The ability to modulate cardiomyocyte contractility is important for bioengineering applications ranging from heart disease treatments to biorobotics. In this study, we examined the changes in contraction frequency of neonatal rat cardiomyocytes upon single-cell-level nanoscale mechanical stimulatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Nagarajan, Neerajha, Vyas, Varun, Huey, Bryan D, Zorlutuna, Pinar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998274/
https://www.ncbi.nlm.nih.gov/pubmed/29942390
http://dx.doi.org/10.1177/1849543516675348
_version_ 1783331214549057536
author Nagarajan, Neerajha
Vyas, Varun
Huey, Bryan D
Zorlutuna, Pinar
author_facet Nagarajan, Neerajha
Vyas, Varun
Huey, Bryan D
Zorlutuna, Pinar
author_sort Nagarajan, Neerajha
collection PubMed
description The ability to modulate cardiomyocyte contractility is important for bioengineering applications ranging from heart disease treatments to biorobotics. In this study, we examined the changes in contraction frequency of neonatal rat cardiomyocytes upon single-cell-level nanoscale mechanical stimulation using atomic force microscopy. To measure the response of same density of cells, they were micropatterned into micropatches of fixed geometry. To examine the effect of the substrate stiffness on the behavior of cells, they were cultured on a stiffer and a softer surface, glass and poly (dimethylsiloxane), respectively. Upon periodic cyclic stimulation of 300 nN at 5 Hz, a significant reduction in the rate of synchronous contraction of the cell patches on poly(dimethylsiloxane) substrates was observed with respect to their spontaneous beat rate, while the cell patches on glass substrates maintained or increased their contraction rate after the stimulation. On the other hand, single cells mostly maintained their contraction rate and could only withstand a lower magnitude of forces compared to micropatterned cell patches. This study reveals that the contraction behavior of cardiomyocytes can be modulated mechanically through cyclic nanomechanical stimulation, and the degree and mode of this modulation depend on the cell connectivity and substrate mechanical properties.
format Online
Article
Text
id pubmed-5998274
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-59982742018-06-25 Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy Nagarajan, Neerajha Vyas, Varun Huey, Bryan D Zorlutuna, Pinar Nanobiomedicine (Rij) Invited Feature Article The ability to modulate cardiomyocyte contractility is important for bioengineering applications ranging from heart disease treatments to biorobotics. In this study, we examined the changes in contraction frequency of neonatal rat cardiomyocytes upon single-cell-level nanoscale mechanical stimulation using atomic force microscopy. To measure the response of same density of cells, they were micropatterned into micropatches of fixed geometry. To examine the effect of the substrate stiffness on the behavior of cells, they were cultured on a stiffer and a softer surface, glass and poly (dimethylsiloxane), respectively. Upon periodic cyclic stimulation of 300 nN at 5 Hz, a significant reduction in the rate of synchronous contraction of the cell patches on poly(dimethylsiloxane) substrates was observed with respect to their spontaneous beat rate, while the cell patches on glass substrates maintained or increased their contraction rate after the stimulation. On the other hand, single cells mostly maintained their contraction rate and could only withstand a lower magnitude of forces compared to micropatterned cell patches. This study reveals that the contraction behavior of cardiomyocytes can be modulated mechanically through cyclic nanomechanical stimulation, and the degree and mode of this modulation depend on the cell connectivity and substrate mechanical properties. SAGE Publications 2016-11-16 /pmc/articles/PMC5998274/ /pubmed/29942390 http://dx.doi.org/10.1177/1849543516675348 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Invited Feature Article
Nagarajan, Neerajha
Vyas, Varun
Huey, Bryan D
Zorlutuna, Pinar
Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title_full Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title_fullStr Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title_full_unstemmed Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title_short Modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
title_sort modulation of the contractility of micropatterned myocardial cells with nanoscale forces using atomic force microscopy
topic Invited Feature Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998274/
https://www.ncbi.nlm.nih.gov/pubmed/29942390
http://dx.doi.org/10.1177/1849543516675348
work_keys_str_mv AT nagarajanneerajha modulationofthecontractilityofmicropatternedmyocardialcellswithnanoscaleforcesusingatomicforcemicroscopy
AT vyasvarun modulationofthecontractilityofmicropatternedmyocardialcellswithnanoscaleforcesusingatomicforcemicroscopy
AT hueybryand modulationofthecontractilityofmicropatternedmyocardialcellswithnanoscaleforcesusingatomicforcemicroscopy
AT zorlutunapinar modulationofthecontractilityofmicropatternedmyocardialcellswithnanoscaleforcesusingatomicforcemicroscopy