Cargando…

Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart

Stem cell therapy has the potential to improve cardiac function after myocardial infarction (MI); however, existing methods to deliver cells to the myocardium, including intramyocardial injection, suffer from low engraftment rates. In this study, we used a rat model of acute MI to assess the effects...

Descripción completa

Detalles Bibliográficos
Autores principales: Hansen, Katrina J., Favreau, John T., Guyette, Jacques P., Tao, Ze-Wei, Coffin, Spencer T., Cunha-Gavidia, Anny, D'Amore, Brian, Perreault, Luke R., Fitzpatrick, John P., DeMartino, Angelica, Gaudette, Glenn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003011/
https://www.ncbi.nlm.nih.gov/pubmed/27610271
http://dx.doi.org/10.1089/biores.2016.0026
_version_ 1782450603674304512
author Hansen, Katrina J.
Favreau, John T.
Guyette, Jacques P.
Tao, Ze-Wei
Coffin, Spencer T.
Cunha-Gavidia, Anny
D'Amore, Brian
Perreault, Luke R.
Fitzpatrick, John P.
DeMartino, Angelica
Gaudette, Glenn R.
author_facet Hansen, Katrina J.
Favreau, John T.
Guyette, Jacques P.
Tao, Ze-Wei
Coffin, Spencer T.
Cunha-Gavidia, Anny
D'Amore, Brian
Perreault, Luke R.
Fitzpatrick, John P.
DeMartino, Angelica
Gaudette, Glenn R.
author_sort Hansen, Katrina J.
collection PubMed
description Stem cell therapy has the potential to improve cardiac function after myocardial infarction (MI); however, existing methods to deliver cells to the myocardium, including intramyocardial injection, suffer from low engraftment rates. In this study, we used a rat model of acute MI to assess the effects of human mesenchymal stem cell (hMSC)-seeded fibrin biological sutures on cardiac function at 1 week after implant. Biological sutures were seeded with quantum dot (Qdot)-loaded hMSCs for 24 h before implantation. At 1 week postinfarct, the heart was imaged to assess mechanical function in the infarct region. Regional parameters assessed were regional stroke work (RSW) and systolic area of contraction (SAC) and global parameters derived from the pressure waveform. MI (n = 6) significantly decreased RSW (0.026 ± 0.011) and SAC (0.022 ± 0.015) when compared with sham operation (RSW: 0.141 ± 0.009; SAC: 0.166 ± 0.005, n = 6) (p < 0.05). The delivery of unseeded biological sutures to the infarcted hearts did not change regional mechanical function compared with the infarcted hearts (RSW: 0.032 ± 0.004, SAC: 0.037 ± 0.008, n = 6). The delivery of hMSC-seeded sutures exerted a trend toward increase of regional mechanical function compared with the infarcted heart (RSW: 0.057 ± 0.011; SAC: 0.051 ± 0.014, n = 6). Global function showed no significant differences between any group (p > 0.05); however, there was a trend toward improved function with the addition of either unseeded or seeded biological suture. Histology demonstrated that Qdot-loaded hMSCs remained present in the infarcted myocardium after 1 week. Analysis of serial sections of Masson's trichrome staining revealed that the greatest infarct size was in the infarct group (7.0% ± 2.2%), where unseeded (3.8% ± 0.6%) and hMSC-seeded (3.7% ± 0.8%) suture groups maintained similar infarct sizes. Furthermore, the remaining suture area was significantly decreased in the unseeded group compared with that in the hMSC-seeded group (p < 0.05). This study demonstrated that hMSC-seeded biological sutures are a method to deliver cells to the infarcted myocardium and have treatment potential.
format Online
Article
Text
id pubmed-5003011
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Mary Ann Liebert, Inc.
record_format MEDLINE/PubMed
spelling pubmed-50030112016-09-08 Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart Hansen, Katrina J. Favreau, John T. Guyette, Jacques P. Tao, Ze-Wei Coffin, Spencer T. Cunha-Gavidia, Anny D'Amore, Brian Perreault, Luke R. Fitzpatrick, John P. DeMartino, Angelica Gaudette, Glenn R. Biores Open Access Original Research Article Stem cell therapy has the potential to improve cardiac function after myocardial infarction (MI); however, existing methods to deliver cells to the myocardium, including intramyocardial injection, suffer from low engraftment rates. In this study, we used a rat model of acute MI to assess the effects of human mesenchymal stem cell (hMSC)-seeded fibrin biological sutures on cardiac function at 1 week after implant. Biological sutures were seeded with quantum dot (Qdot)-loaded hMSCs for 24 h before implantation. At 1 week postinfarct, the heart was imaged to assess mechanical function in the infarct region. Regional parameters assessed were regional stroke work (RSW) and systolic area of contraction (SAC) and global parameters derived from the pressure waveform. MI (n = 6) significantly decreased RSW (0.026 ± 0.011) and SAC (0.022 ± 0.015) when compared with sham operation (RSW: 0.141 ± 0.009; SAC: 0.166 ± 0.005, n = 6) (p < 0.05). The delivery of unseeded biological sutures to the infarcted hearts did not change regional mechanical function compared with the infarcted hearts (RSW: 0.032 ± 0.004, SAC: 0.037 ± 0.008, n = 6). The delivery of hMSC-seeded sutures exerted a trend toward increase of regional mechanical function compared with the infarcted heart (RSW: 0.057 ± 0.011; SAC: 0.051 ± 0.014, n = 6). Global function showed no significant differences between any group (p > 0.05); however, there was a trend toward improved function with the addition of either unseeded or seeded biological suture. Histology demonstrated that Qdot-loaded hMSCs remained present in the infarcted myocardium after 1 week. Analysis of serial sections of Masson's trichrome staining revealed that the greatest infarct size was in the infarct group (7.0% ± 2.2%), where unseeded (3.8% ± 0.6%) and hMSC-seeded (3.7% ± 0.8%) suture groups maintained similar infarct sizes. Furthermore, the remaining suture area was significantly decreased in the unseeded group compared with that in the hMSC-seeded group (p < 0.05). This study demonstrated that hMSC-seeded biological sutures are a method to deliver cells to the infarcted myocardium and have treatment potential. Mary Ann Liebert, Inc. 2016-08-01 /pmc/articles/PMC5003011/ /pubmed/27610271 http://dx.doi.org/10.1089/biores.2016.0026 Text en © Katrina J. Hansen et al. 2016; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Original Research Article
Hansen, Katrina J.
Favreau, John T.
Guyette, Jacques P.
Tao, Ze-Wei
Coffin, Spencer T.
Cunha-Gavidia, Anny
D'Amore, Brian
Perreault, Luke R.
Fitzpatrick, John P.
DeMartino, Angelica
Gaudette, Glenn R.
Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title_full Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title_fullStr Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title_full_unstemmed Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title_short Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart
title_sort functional effects of delivering human mesenchymal stem cell-seeded biological sutures to an infarcted heart
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003011/
https://www.ncbi.nlm.nih.gov/pubmed/27610271
http://dx.doi.org/10.1089/biores.2016.0026
work_keys_str_mv AT hansenkatrinaj functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT favreaujohnt functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT guyettejacquesp functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT taozewei functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT coffinspencert functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT cunhagavidiaanny functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT damorebrian functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT perreaultluker functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT fitzpatrickjohnp functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT demartinoangelica functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart
AT gaudetteglennr functionaleffectsofdeliveringhumanmesenchymalstemcellseededbiologicalsuturestoaninfarctedheart