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Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia

Bronchopulmonary dysplasia (BPD) is a devastating lung condition that develops in premature newborns exposed to prolonged mechanical ventilation and supplemental oxygen. Significant morbidity and mortality are associated with this costly disease and effective therapies are limited. Mesenchymal stem/...

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Autores principales: Moreira, Alvaro, Winter, Caitlyn, Joy, Jooby, Winter, Lauryn, Jones, Maxwell, Noronha, Michelle, Porter, Melissa, Quim, Kayla, Corral, Alexis, Alayli, Yasmeen, Seno, Tyrelle, Mustafa, Shamimunisa, Hornsby, Peter, Ahuja, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988765/
https://www.ncbi.nlm.nih.gov/pubmed/31774626
http://dx.doi.org/10.1002/sctm.18-0273
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author Moreira, Alvaro
Winter, Caitlyn
Joy, Jooby
Winter, Lauryn
Jones, Maxwell
Noronha, Michelle
Porter, Melissa
Quim, Kayla
Corral, Alexis
Alayli, Yasmeen
Seno, Tyrelle
Mustafa, Shamimunisa
Hornsby, Peter
Ahuja, Sunil
author_facet Moreira, Alvaro
Winter, Caitlyn
Joy, Jooby
Winter, Lauryn
Jones, Maxwell
Noronha, Michelle
Porter, Melissa
Quim, Kayla
Corral, Alexis
Alayli, Yasmeen
Seno, Tyrelle
Mustafa, Shamimunisa
Hornsby, Peter
Ahuja, Sunil
author_sort Moreira, Alvaro
collection PubMed
description Bronchopulmonary dysplasia (BPD) is a devastating lung condition that develops in premature newborns exposed to prolonged mechanical ventilation and supplemental oxygen. Significant morbidity and mortality are associated with this costly disease and effective therapies are limited. Mesenchymal stem/stromal cells (MSCs) are multipotent cells that can repair injured tissue by secreting paracrine factors known to restore the function and integrity of injured lung epithelium and endothelium. Most preclinical studies showing therapeutic efficacy of MSCs for BPD are administered either intratracheally or intravenously. The purpose of this study was to examine the feasibility and effectiveness of human cord tissue‐derived MSC administration given via the intranasal route. Human umbilical cord tissue MSCs were isolated, characterized, and given intranasally (500 000 cells per 20 μL) to a hyperoxia‐induced rat model of BPD. Lung alveolarization, vascularization, and pulmonary vascular remodeling were restored in animals receiving MSC treatment. Gene and protein analysis suggest the beneficial effects of MSCs were attributed, in part, to a concerted effort targeting angiogenesis, immunomodulation, wound healing, and cell survival. These findings are clinically significant, as neonates who develop BPD have altered alveolar development, decreased pulmonary vascularization and chronic inflammation, all resulting in impaired tissue healing. Our study is the first to report the intranasal delivery of umbilical cord Wharton's jelly MSCs in experimental BPD is feasible, noninvasive, and an effective route that may bear clinical applicability.
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spelling pubmed-69887652020-02-03 Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia Moreira, Alvaro Winter, Caitlyn Joy, Jooby Winter, Lauryn Jones, Maxwell Noronha, Michelle Porter, Melissa Quim, Kayla Corral, Alexis Alayli, Yasmeen Seno, Tyrelle Mustafa, Shamimunisa Hornsby, Peter Ahuja, Sunil Stem Cells Transl Med Fetal and Neonatal Stem Cells Bronchopulmonary dysplasia (BPD) is a devastating lung condition that develops in premature newborns exposed to prolonged mechanical ventilation and supplemental oxygen. Significant morbidity and mortality are associated with this costly disease and effective therapies are limited. Mesenchymal stem/stromal cells (MSCs) are multipotent cells that can repair injured tissue by secreting paracrine factors known to restore the function and integrity of injured lung epithelium and endothelium. Most preclinical studies showing therapeutic efficacy of MSCs for BPD are administered either intratracheally or intravenously. The purpose of this study was to examine the feasibility and effectiveness of human cord tissue‐derived MSC administration given via the intranasal route. Human umbilical cord tissue MSCs were isolated, characterized, and given intranasally (500 000 cells per 20 μL) to a hyperoxia‐induced rat model of BPD. Lung alveolarization, vascularization, and pulmonary vascular remodeling were restored in animals receiving MSC treatment. Gene and protein analysis suggest the beneficial effects of MSCs were attributed, in part, to a concerted effort targeting angiogenesis, immunomodulation, wound healing, and cell survival. These findings are clinically significant, as neonates who develop BPD have altered alveolar development, decreased pulmonary vascularization and chronic inflammation, all resulting in impaired tissue healing. Our study is the first to report the intranasal delivery of umbilical cord Wharton's jelly MSCs in experimental BPD is feasible, noninvasive, and an effective route that may bear clinical applicability. John Wiley & Sons, Inc. 2019-11-27 /pmc/articles/PMC6988765/ /pubmed/31774626 http://dx.doi.org/10.1002/sctm.18-0273 Text en © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Fetal and Neonatal Stem Cells
Moreira, Alvaro
Winter, Caitlyn
Joy, Jooby
Winter, Lauryn
Jones, Maxwell
Noronha, Michelle
Porter, Melissa
Quim, Kayla
Corral, Alexis
Alayli, Yasmeen
Seno, Tyrelle
Mustafa, Shamimunisa
Hornsby, Peter
Ahuja, Sunil
Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title_full Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title_fullStr Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title_full_unstemmed Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title_short Intranasal delivery of human umbilical cord Wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
title_sort intranasal delivery of human umbilical cord wharton's jelly mesenchymal stromal cells restores lung alveolarization and vascularization in experimental bronchopulmonary dysplasia
topic Fetal and Neonatal Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988765/
https://www.ncbi.nlm.nih.gov/pubmed/31774626
http://dx.doi.org/10.1002/sctm.18-0273
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