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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |