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Encapsulation of macrophages enhances their retention and angiogenic potential

Cell therapies to treat critical limb ischaemia have demonstrated only modest results in clinical trials, and this has been partly attributed to poor cell retention following their delivery directly into the ischaemic limb. The aim of this study was to determine whether alginate encapsulation of the...

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Autores principales: Ludwinski, Francesca E., Patel, Ashish S., Damodaran, Gopinath, Cho, Jun, Furmston, Joanna, Xu, Qingbo, Jayasinghe, Suwan N., Smith, Alberto, Modarai, Bijan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426993/
https://www.ncbi.nlm.nih.gov/pubmed/30911410
http://dx.doi.org/10.1038/s41536-019-0068-5
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author Ludwinski, Francesca E.
Patel, Ashish S.
Damodaran, Gopinath
Cho, Jun
Furmston, Joanna
Xu, Qingbo
Jayasinghe, Suwan N.
Smith, Alberto
Modarai, Bijan
author_facet Ludwinski, Francesca E.
Patel, Ashish S.
Damodaran, Gopinath
Cho, Jun
Furmston, Joanna
Xu, Qingbo
Jayasinghe, Suwan N.
Smith, Alberto
Modarai, Bijan
author_sort Ludwinski, Francesca E.
collection PubMed
description Cell therapies to treat critical limb ischaemia have demonstrated only modest results in clinical trials, and this has been partly attributed to poor cell retention following their delivery directly into the ischaemic limb. The aim of this study was to determine whether alginate encapsulation of therapeutic pro-angio/arteriogenic macrophages enhances their retention and ultimately improves limb perfusion. A reproducible GMP-compliant method for generating 300 µm alginate capsules was developed to encapsulate pro-angio/arteriogenic macrophages. Longitudinal analysis revealed no detrimental effect of encapsulation on cell number or viability in vitro, and macrophages retained their pro-angio/arteriogenic phenotype. Intramuscular delivery of encapsulated macrophages into the murine ischaemic hindlimb demonstrated increased cell retention compared with injection of naked cells (P = 0.0001), and that this was associated both enhanced angiogenesis (P = 0.02) and arteriogenesis (P = 0.03), and an overall improvement in limb perfusion (P = 0.0001). Alginate encapsulation of pro-angio/arteriogenic macrophages enhances cell retention and subsequent limb reperfusion in vivo. Encapsulation may therefore represent a means of improving the efficacy of cell-based therapies currently under investigation for the treatment of limb ischaemia.
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spelling pubmed-64269932019-03-25 Encapsulation of macrophages enhances their retention and angiogenic potential Ludwinski, Francesca E. Patel, Ashish S. Damodaran, Gopinath Cho, Jun Furmston, Joanna Xu, Qingbo Jayasinghe, Suwan N. Smith, Alberto Modarai, Bijan NPJ Regen Med Article Cell therapies to treat critical limb ischaemia have demonstrated only modest results in clinical trials, and this has been partly attributed to poor cell retention following their delivery directly into the ischaemic limb. The aim of this study was to determine whether alginate encapsulation of therapeutic pro-angio/arteriogenic macrophages enhances their retention and ultimately improves limb perfusion. A reproducible GMP-compliant method for generating 300 µm alginate capsules was developed to encapsulate pro-angio/arteriogenic macrophages. Longitudinal analysis revealed no detrimental effect of encapsulation on cell number or viability in vitro, and macrophages retained their pro-angio/arteriogenic phenotype. Intramuscular delivery of encapsulated macrophages into the murine ischaemic hindlimb demonstrated increased cell retention compared with injection of naked cells (P = 0.0001), and that this was associated both enhanced angiogenesis (P = 0.02) and arteriogenesis (P = 0.03), and an overall improvement in limb perfusion (P = 0.0001). Alginate encapsulation of pro-angio/arteriogenic macrophages enhances cell retention and subsequent limb reperfusion in vivo. Encapsulation may therefore represent a means of improving the efficacy of cell-based therapies currently under investigation for the treatment of limb ischaemia. Nature Publishing Group UK 2019-03-20 /pmc/articles/PMC6426993/ /pubmed/30911410 http://dx.doi.org/10.1038/s41536-019-0068-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ludwinski, Francesca E.
Patel, Ashish S.
Damodaran, Gopinath
Cho, Jun
Furmston, Joanna
Xu, Qingbo
Jayasinghe, Suwan N.
Smith, Alberto
Modarai, Bijan
Encapsulation of macrophages enhances their retention and angiogenic potential
title Encapsulation of macrophages enhances their retention and angiogenic potential
title_full Encapsulation of macrophages enhances their retention and angiogenic potential
title_fullStr Encapsulation of macrophages enhances their retention and angiogenic potential
title_full_unstemmed Encapsulation of macrophages enhances their retention and angiogenic potential
title_short Encapsulation of macrophages enhances their retention and angiogenic potential
title_sort encapsulation of macrophages enhances their retention and angiogenic potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426993/
https://www.ncbi.nlm.nih.gov/pubmed/30911410
http://dx.doi.org/10.1038/s41536-019-0068-5
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