Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes
Cardiomyocytes derived from human stem cells are quickly becoming mainstays of cardiac regenerative medicine, in vitro disease modeling, and drug screening. Their suitability for such roles may seem obvious, but assessments of their contractile behavior suggest that they have not achieved a complete...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2015-01-01
|
Series: | Biomarker Insights |
Online Access: | https://doi.org/10.4137/BMI.S23912 |
id |
doaj-1b6bbd3d3c9349efaff0305da930cd8b |
---|---|
record_format |
Article |
spelling |
doaj-1b6bbd3d3c9349efaff0305da930cd8b2020-11-25T03:22:13ZengSAGE PublishingBiomarker Insights1177-27192015-01-0110s110.4137/BMI.S23912Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac MyocytesJonas Schwan0Stuart G. Campbell1Department of Biomedical Engineering, Yale University, New Haven, CT, USA.Department of Biomedical Engineering, Yale University, New Haven, CT, USA.Cardiomyocytes derived from human stem cells are quickly becoming mainstays of cardiac regenerative medicine, in vitro disease modeling, and drug screening. Their suitability for such roles may seem obvious, but assessments of their contractile behavior suggest that they have not achieved a completely mature cardiac muscle phenotype. This could be explained in part by an incomplete transition from fetal to adult myofilament protein isoform expression. In this commentary, we review evidence that supports this hypothesis and discuss prospects for ultimately generating engineered heart tissue specimens that behave similarly to adult human myocardium. We suggest approaches to better characterize myofilament maturation level in these in vitro systems, and illustrate how new computational models could be used to better understand complex relationships between muscle contraction, myofilament protein isoform expression, and maturation.https://doi.org/10.4137/BMI.S23912 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jonas Schwan Stuart G. Campbell |
spellingShingle |
Jonas Schwan Stuart G. Campbell Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes Biomarker Insights |
author_facet |
Jonas Schwan Stuart G. Campbell |
author_sort |
Jonas Schwan |
title |
Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes |
title_short |
Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes |
title_full |
Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes |
title_fullStr |
Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes |
title_full_unstemmed |
Article Commentary: Prospects for Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes |
title_sort |
article commentary: prospects for myofilament maturation in stem cell-derived cardiac myocytes |
publisher |
SAGE Publishing |
series |
Biomarker Insights |
issn |
1177-2719 |
publishDate |
2015-01-01 |
description |
Cardiomyocytes derived from human stem cells are quickly becoming mainstays of cardiac regenerative medicine, in vitro disease modeling, and drug screening. Their suitability for such roles may seem obvious, but assessments of their contractile behavior suggest that they have not achieved a completely mature cardiac muscle phenotype. This could be explained in part by an incomplete transition from fetal to adult myofilament protein isoform expression. In this commentary, we review evidence that supports this hypothesis and discuss prospects for ultimately generating engineered heart tissue specimens that behave similarly to adult human myocardium. We suggest approaches to better characterize myofilament maturation level in these in vitro systems, and illustrate how new computational models could be used to better understand complex relationships between muscle contraction, myofilament protein isoform expression, and maturation. |
url |
https://doi.org/10.4137/BMI.S23912 |
work_keys_str_mv |
AT jonasschwan articlecommentaryprospectsformyofilamentmaturationinstemcellderivedcardiacmyocytes AT stuartgcampbell articlecommentaryprospectsformyofilamentmaturationinstemcellderivedcardiacmyocytes |
_version_ |
1724610573485735936 |