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Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment

[Image: see text] Retention and survival of transplanted cells are major limitations to the efficacy of regenerative medicine, with short-term paracrine signals being the principal mechanism underlying current cell therapies for heart repair. Consequently, even improvements in short-term durability...

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Autores principales: Speidel, Alessondra T., Stuckey, Daniel J., Chow, Lesley W., Jackson, Laurence H., Noseda, Michela, Abreu Paiva, Marta, Schneider, Michael D., Stevens, Molly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408339/
https://www.ncbi.nlm.nih.gov/pubmed/28470052
http://dx.doi.org/10.1021/acscentsci.7b00039
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author Speidel, Alessondra T.
Stuckey, Daniel J.
Chow, Lesley W.
Jackson, Laurence H.
Noseda, Michela
Abreu Paiva, Marta
Schneider, Michael D.
Stevens, Molly M.
author_facet Speidel, Alessondra T.
Stuckey, Daniel J.
Chow, Lesley W.
Jackson, Laurence H.
Noseda, Michela
Abreu Paiva, Marta
Schneider, Michael D.
Stevens, Molly M.
author_sort Speidel, Alessondra T.
collection PubMed
description [Image: see text] Retention and survival of transplanted cells are major limitations to the efficacy of regenerative medicine, with short-term paracrine signals being the principal mechanism underlying current cell therapies for heart repair. Consequently, even improvements in short-term durability may have a potential impact on cardiac cell grafting. We have developed a multimodal hydrogel-based platform comprised of a poly(ethylene glycol) network cross-linked with bioactive peptides functionalized with Gd(III) in order to monitor the localization and retention of the hydrogel in vivo by magnetic resonance imaging. In this study, we have tailored the material for cardiac applications through the inclusion of a heparin-binding peptide (HBP) sequence in the cross-linker design and formulated the gel to display mechanical properties resembling those of cardiac tissue. Luciferase-expressing cardiac stem cells (CSC-Luc2) encapsulated within these gels maintained their metabolic activity for up to 14 days in vitro. Encapsulation in the HBP hydrogels improved CSC-Luc2 retention in the mouse myocardium and hind limbs at 3 days by 6.5- and 12- fold, respectively. Thus, this novel heparin-binding based, Gd(III)-tagged hydrogel and CSC-Luc2 platform system demonstrates a tailored, in vivo detectable theranostic cell delivery system that can be implemented to monitor and assess the transplanted material and cell retention.
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spelling pubmed-54083392017-05-03 Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment Speidel, Alessondra T. Stuckey, Daniel J. Chow, Lesley W. Jackson, Laurence H. Noseda, Michela Abreu Paiva, Marta Schneider, Michael D. Stevens, Molly M. ACS Cent Sci [Image: see text] Retention and survival of transplanted cells are major limitations to the efficacy of regenerative medicine, with short-term paracrine signals being the principal mechanism underlying current cell therapies for heart repair. Consequently, even improvements in short-term durability may have a potential impact on cardiac cell grafting. We have developed a multimodal hydrogel-based platform comprised of a poly(ethylene glycol) network cross-linked with bioactive peptides functionalized with Gd(III) in order to monitor the localization and retention of the hydrogel in vivo by magnetic resonance imaging. In this study, we have tailored the material for cardiac applications through the inclusion of a heparin-binding peptide (HBP) sequence in the cross-linker design and formulated the gel to display mechanical properties resembling those of cardiac tissue. Luciferase-expressing cardiac stem cells (CSC-Luc2) encapsulated within these gels maintained their metabolic activity for up to 14 days in vitro. Encapsulation in the HBP hydrogels improved CSC-Luc2 retention in the mouse myocardium and hind limbs at 3 days by 6.5- and 12- fold, respectively. Thus, this novel heparin-binding based, Gd(III)-tagged hydrogel and CSC-Luc2 platform system demonstrates a tailored, in vivo detectable theranostic cell delivery system that can be implemented to monitor and assess the transplanted material and cell retention. American Chemical Society 2017-03-30 2017-04-26 /pmc/articles/PMC5408339/ /pubmed/28470052 http://dx.doi.org/10.1021/acscentsci.7b00039 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Speidel, Alessondra T.
Stuckey, Daniel J.
Chow, Lesley W.
Jackson, Laurence H.
Noseda, Michela
Abreu Paiva, Marta
Schneider, Michael D.
Stevens, Molly M.
Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title_full Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title_fullStr Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title_full_unstemmed Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title_short Multimodal Hydrogel-Based Platform To Deliver and Monitor Cardiac Progenitor/Stem Cell Engraftment
title_sort multimodal hydrogel-based platform to deliver and monitor cardiac progenitor/stem cell engraftment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408339/
https://www.ncbi.nlm.nih.gov/pubmed/28470052
http://dx.doi.org/10.1021/acscentsci.7b00039
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