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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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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. |
format | Online Article Text |
id | pubmed-4751100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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