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Macrophage-Engineered Vesicles for Therapeutic Delivery and Bidirectional Reprogramming of Immune Cell Polarization
[Image: see text] Macrophages, one of the most important phagocytic cells of the immune system, are highly plastic and are known to exhibit diverse roles under different pathological conditions. The ability to repolarize macrophages from pro-inflammatory (M1) to anti-inflammatory (M2) or vice versa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876833/ https://www.ncbi.nlm.nih.gov/pubmed/33585763 http://dx.doi.org/10.1021/acsomega.0c05632 |
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author | Neupane, Khaga R. McCorkle, J. Robert Kopper, Timothy J. Lakes, Jourdan E. Aryal, Surya P. Abdullah, Masud Snell, Aaron A. Gensel, John C. Kolesar, Jill Richards, Christopher I. |
author_facet | Neupane, Khaga R. McCorkle, J. Robert Kopper, Timothy J. Lakes, Jourdan E. Aryal, Surya P. Abdullah, Masud Snell, Aaron A. Gensel, John C. Kolesar, Jill Richards, Christopher I. |
author_sort | Neupane, Khaga R. |
collection | PubMed |
description | [Image: see text] Macrophages, one of the most important phagocytic cells of the immune system, are highly plastic and are known to exhibit diverse roles under different pathological conditions. The ability to repolarize macrophages from pro-inflammatory (M1) to anti-inflammatory (M2) or vice versa offers a promising therapeutic approach for treating various diseases such as traumatic injury and cancer. Herein, it is demonstrated that macrophage-engineered vesicles (MEVs) generated by disruption of macrophage cellular membranes can be used as nanocarriers capable of reprogramming macrophages and microglia toward either pro- or anti-inflammatory phenotypes. MEVs can be produced at high yields and easily loaded with diagnostic molecules or chemotherapeutics and delivered to both macrophages and cancer cells in vitro and in vivo. Overall, MEVs show promise as potential delivery vehicles for both therapeutics and their ability to controllably modulate macrophage/microglia inflammatory phenotypes. |
format | Online Article Text |
id | pubmed-7876833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78768332021-02-12 Macrophage-Engineered Vesicles for Therapeutic Delivery and Bidirectional Reprogramming of Immune Cell Polarization Neupane, Khaga R. McCorkle, J. Robert Kopper, Timothy J. Lakes, Jourdan E. Aryal, Surya P. Abdullah, Masud Snell, Aaron A. Gensel, John C. Kolesar, Jill Richards, Christopher I. ACS Omega [Image: see text] Macrophages, one of the most important phagocytic cells of the immune system, are highly plastic and are known to exhibit diverse roles under different pathological conditions. The ability to repolarize macrophages from pro-inflammatory (M1) to anti-inflammatory (M2) or vice versa offers a promising therapeutic approach for treating various diseases such as traumatic injury and cancer. Herein, it is demonstrated that macrophage-engineered vesicles (MEVs) generated by disruption of macrophage cellular membranes can be used as nanocarriers capable of reprogramming macrophages and microglia toward either pro- or anti-inflammatory phenotypes. MEVs can be produced at high yields and easily loaded with diagnostic molecules or chemotherapeutics and delivered to both macrophages and cancer cells in vitro and in vivo. Overall, MEVs show promise as potential delivery vehicles for both therapeutics and their ability to controllably modulate macrophage/microglia inflammatory phenotypes. American Chemical Society 2021-01-26 /pmc/articles/PMC7876833/ /pubmed/33585763 http://dx.doi.org/10.1021/acsomega.0c05632 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Neupane, Khaga R. McCorkle, J. Robert Kopper, Timothy J. Lakes, Jourdan E. Aryal, Surya P. Abdullah, Masud Snell, Aaron A. Gensel, John C. Kolesar, Jill Richards, Christopher I. Macrophage-Engineered Vesicles for Therapeutic Delivery and Bidirectional Reprogramming of Immune Cell Polarization |
title | Macrophage-Engineered Vesicles for Therapeutic Delivery
and Bidirectional Reprogramming of Immune Cell Polarization |
title_full | Macrophage-Engineered Vesicles for Therapeutic Delivery
and Bidirectional Reprogramming of Immune Cell Polarization |
title_fullStr | Macrophage-Engineered Vesicles for Therapeutic Delivery
and Bidirectional Reprogramming of Immune Cell Polarization |
title_full_unstemmed | Macrophage-Engineered Vesicles for Therapeutic Delivery
and Bidirectional Reprogramming of Immune Cell Polarization |
title_short | Macrophage-Engineered Vesicles for Therapeutic Delivery
and Bidirectional Reprogramming of Immune Cell Polarization |
title_sort | macrophage-engineered vesicles for therapeutic delivery
and bidirectional reprogramming of immune cell polarization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876833/ https://www.ncbi.nlm.nih.gov/pubmed/33585763 http://dx.doi.org/10.1021/acsomega.0c05632 |
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