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Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?

Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly...

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Autores principales: Mueller, Martin, Wolfs, Tim G. A., Schoeberlein, Andreina, Gavilanes, Antonio W. D., Surbek, Daniel, Kramer, Boris W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751100/
https://www.ncbi.nlm.nih.gov/pubmed/26869264
http://dx.doi.org/10.1186/s40348-016-0034-x
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author Mueller, Martin
Wolfs, Tim G. A.
Schoeberlein, Andreina
Gavilanes, Antonio W. D.
Surbek, Daniel
Kramer, Boris W.
author_facet Mueller, Martin
Wolfs, Tim G. A.
Schoeberlein, Andreina
Gavilanes, Antonio W. D.
Surbek, Daniel
Kramer, Boris W.
author_sort Mueller, Martin
collection PubMed
description Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. While advances in perinatal medicine have improved our understanding of the pathogenesis, effective therapies to prevent and/or reduce the severity of these disorders are still lacking. The potential of mesenchymal stem/stromal cell (MSC) therapy has emerged during the last two decades, and an increasing effort is conducted to address brain- and lung-related morbidities in neonates at risk. Various studies support the notion that MSCs have protective effects. MSCs are an easy source and may be readily available after birth in a clinical setting. MSCs’ mechanisms of action are diverse, including migration and homing, release of growth factors and immunomodulation, and the potential to replace injured cells. Here, we review the pathophysiology of perinatally acquired brain and lung injuries and focus on MSCs as potential candidates for therapeutic strategies summarizing preclinical and clinical evidence.
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spelling pubmed-47511002016-02-22 Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity? Mueller, Martin Wolfs, Tim G. A. Schoeberlein, Andreina Gavilanes, Antonio W. D. Surbek, Daniel Kramer, Boris W. Mol Cell Pediatr Mini Review Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. While advances in perinatal medicine have improved our understanding of the pathogenesis, effective therapies to prevent and/or reduce the severity of these disorders are still lacking. The potential of mesenchymal stem/stromal cell (MSC) therapy has emerged during the last two decades, and an increasing effort is conducted to address brain- and lung-related morbidities in neonates at risk. Various studies support the notion that MSCs have protective effects. MSCs are an easy source and may be readily available after birth in a clinical setting. MSCs’ mechanisms of action are diverse, including migration and homing, release of growth factors and immunomodulation, and the potential to replace injured cells. Here, we review the pathophysiology of perinatally acquired brain and lung injuries and focus on MSCs as potential candidates for therapeutic strategies summarizing preclinical and clinical evidence. Springer Berlin Heidelberg 2016-02-11 /pmc/articles/PMC4751100/ /pubmed/26869264 http://dx.doi.org/10.1186/s40348-016-0034-x Text en © Mueller et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Mini Review
Mueller, Martin
Wolfs, Tim G. A.
Schoeberlein, Andreina
Gavilanes, Antonio W. D.
Surbek, Daniel
Kramer, Boris W.
Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title_full Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title_fullStr Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title_full_unstemmed Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title_short Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
title_sort mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751100/
https://www.ncbi.nlm.nih.gov/pubmed/26869264
http://dx.doi.org/10.1186/s40348-016-0034-x
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