Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain

The heart has a dynamic mechanical environment contributed by its unique cellular composition and the resultant complex tissue structure. In pathological heart tissue, both the mechanics and cell composition can change and influence each other. As a result, the interplay between the cell phenotype a...

Full description

Bibliographic Details
Main Authors: Richard Duc Hien Tran, Tessa Altair Morris, Daniela Gonzalez, Ali Hatem Salaheldin Hassan Ahmed Hetta, Anna Grosberg
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/11/3199
_version_ 1797510775854596096
author Richard Duc Hien Tran
Tessa Altair Morris
Daniela Gonzalez
Ali Hatem Salaheldin Hassan Ahmed Hetta
Anna Grosberg
author_facet Richard Duc Hien Tran
Tessa Altair Morris
Daniela Gonzalez
Ali Hatem Salaheldin Hassan Ahmed Hetta
Anna Grosberg
author_sort Richard Duc Hien Tran
collection DOAJ
description The heart has a dynamic mechanical environment contributed by its unique cellular composition and the resultant complex tissue structure. In pathological heart tissue, both the mechanics and cell composition can change and influence each other. As a result, the interplay between the cell phenotype and mechanical stimulation needs to be considered to understand the biophysical cell interactions and organization in healthy and diseased myocardium. In this work, we hypothesized that the overall tissue organization is controlled by varying densities of cardiomyocytes and fibroblasts in the heart. In order to test this hypothesis, we utilized a combination of mechanical strain, co-cultures of different cell types, and inhibitory drugs that block intercellular junction formation. To accomplish this, an image analysis pipeline was developed to automatically measure cell type-specific organization relative to the stretch direction. The results indicated that cardiac cell type-specific densities influence the overall organization of heart tissue such that it is possible to model healthy and fibrotic heart tissue in vitro. This study provides insight into how to mimic the dynamic mechanical environment of the heart in engineered tissue as well as providing valuable information about the process of cardiac remodeling and repair in diseased hearts.
first_indexed 2024-03-10T05:36:04Z
format Article
id doaj.art-22261ae217ab43078f7ab74e0860efd7
institution Directory Open Access Journal
issn 2073-4409
language English
last_indexed 2024-03-10T05:36:04Z
publishDate 2021-11-01
publisher MDPI AG
record_format Article
series Cells
spelling doaj.art-22261ae217ab43078f7ab74e0860efd72023-11-22T22:52:45ZengMDPI AGCells2073-44092021-11-011011319910.3390/cells10113199Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic StrainRichard Duc Hien Tran0Tessa Altair Morris1Daniela Gonzalez2Ali Hatem Salaheldin Hassan Ahmed Hetta3Anna Grosberg4Edwards Lifesciences Center for Advanced Cardiovascular Technology, University of California, Irvine, CA 92617-2700, USAEdwards Lifesciences Center for Advanced Cardiovascular Technology, University of California, Irvine, CA 92617-2700, USAEdwards Lifesciences Center for Advanced Cardiovascular Technology, University of California, Irvine, CA 92617-2700, USAEdwards Lifesciences Center for Advanced Cardiovascular Technology, University of California, Irvine, CA 92617-2700, USAEdwards Lifesciences Center for Advanced Cardiovascular Technology, University of California, Irvine, CA 92617-2700, USAThe heart has a dynamic mechanical environment contributed by its unique cellular composition and the resultant complex tissue structure. In pathological heart tissue, both the mechanics and cell composition can change and influence each other. As a result, the interplay between the cell phenotype and mechanical stimulation needs to be considered to understand the biophysical cell interactions and organization in healthy and diseased myocardium. In this work, we hypothesized that the overall tissue organization is controlled by varying densities of cardiomyocytes and fibroblasts in the heart. In order to test this hypothesis, we utilized a combination of mechanical strain, co-cultures of different cell types, and inhibitory drugs that block intercellular junction formation. To accomplish this, an image analysis pipeline was developed to automatically measure cell type-specific organization relative to the stretch direction. The results indicated that cardiac cell type-specific densities influence the overall organization of heart tissue such that it is possible to model healthy and fibrotic heart tissue in vitro. This study provides insight into how to mimic the dynamic mechanical environment of the heart in engineered tissue as well as providing valuable information about the process of cardiac remodeling and repair in diseased hearts.https://www.mdpi.com/2073-4409/10/11/3199heart tissue organizationcell type classificationcyclic strainintercellular junctions
spellingShingle Richard Duc Hien Tran
Tessa Altair Morris
Daniela Gonzalez
Ali Hatem Salaheldin Hassan Ahmed Hetta
Anna Grosberg
Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
Cells
heart tissue organization
cell type classification
cyclic strain
intercellular junctions
title Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
title_full Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
title_fullStr Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
title_full_unstemmed Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
title_short Quantitative Evaluation of Cardiac Cell Interactions and Responses to Cyclic Strain
title_sort quantitative evaluation of cardiac cell interactions and responses to cyclic strain
topic heart tissue organization
cell type classification
cyclic strain
intercellular junctions
url https://www.mdpi.com/2073-4409/10/11/3199
work_keys_str_mv AT richardduchientran quantitativeevaluationofcardiaccellinteractionsandresponsestocyclicstrain
AT tessaaltairmorris quantitativeevaluationofcardiaccellinteractionsandresponsestocyclicstrain
AT danielagonzalez quantitativeevaluationofcardiaccellinteractionsandresponsestocyclicstrain
AT alihatemsalaheldinhassanahmedhetta quantitativeevaluationofcardiaccellinteractionsandresponsestocyclicstrain
AT annagrosberg quantitativeevaluationofcardiaccellinteractionsandresponsestocyclicstrain