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Mesenchymal stromal/stem cells and bronchopulmonary dysplasia
Bronchopulmonary dysplasia (BPD) is a common complication in preterm infants, leading to chronic respiratory disease. There has been an improvement in perinatal care, but many infants still suffer from impaired branching morphogenesis, alveolarization, and pulmonary capillary formation, causing lung...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642488/ https://www.ncbi.nlm.nih.gov/pubmed/37965579 http://dx.doi.org/10.3389/fcell.2023.1247339 |
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author | Zhang, Shuqing Mulder, Cassidy Riddle, Suzette Song, Rui Yue, Dongmei |
author_facet | Zhang, Shuqing Mulder, Cassidy Riddle, Suzette Song, Rui Yue, Dongmei |
author_sort | Zhang, Shuqing |
collection | PubMed |
description | Bronchopulmonary dysplasia (BPD) is a common complication in preterm infants, leading to chronic respiratory disease. There has been an improvement in perinatal care, but many infants still suffer from impaired branching morphogenesis, alveolarization, and pulmonary capillary formation, causing lung function impairments and BPD. There is an increased risk of respiratory infections, pulmonary hypertension, and neurodevelopmental delays in infants with BPD, all of which can lead to long-term morbidity and mortality. Unfortunately, treatment options for Bronchopulmonary dysplasia are limited. A growing body of evidence indicates that mesenchymal stromal/stem cells (MSCs) can treat various lung diseases in regenerative medicine. MSCs are multipotent cells that can differentiate into multiple cell types, including lung cells, and possess immunomodulatory, anti-inflammatory, antioxidative stress, and regenerative properties. MSCs are regulated by mitochondrial function, as well as oxidant stress responses. Maintaining mitochondrial homeostasis will likely be key for MSCs to stimulate proper lung development and regeneration in Bronchopulmonary dysplasia. In recent years, MSCs have demonstrated promising results in treating and preventing bronchopulmonary dysplasia. Studies have shown that MSC therapy can reduce inflammation, mitochondrial impairment, lung injury, and fibrosis. In light of this, MSCs have emerged as a potential therapeutic option for treating Bronchopulmonary dysplasia. The article explores the role of MSCs in lung development and disease, summarizes MSC therapy’s effectiveness in treating Bronchopulmonary dysplasia, and delves into the mechanisms behind this treatment. |
format | Online Article Text |
id | pubmed-10642488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106424882023-11-14 Mesenchymal stromal/stem cells and bronchopulmonary dysplasia Zhang, Shuqing Mulder, Cassidy Riddle, Suzette Song, Rui Yue, Dongmei Front Cell Dev Biol Cell and Developmental Biology Bronchopulmonary dysplasia (BPD) is a common complication in preterm infants, leading to chronic respiratory disease. There has been an improvement in perinatal care, but many infants still suffer from impaired branching morphogenesis, alveolarization, and pulmonary capillary formation, causing lung function impairments and BPD. There is an increased risk of respiratory infections, pulmonary hypertension, and neurodevelopmental delays in infants with BPD, all of which can lead to long-term morbidity and mortality. Unfortunately, treatment options for Bronchopulmonary dysplasia are limited. A growing body of evidence indicates that mesenchymal stromal/stem cells (MSCs) can treat various lung diseases in regenerative medicine. MSCs are multipotent cells that can differentiate into multiple cell types, including lung cells, and possess immunomodulatory, anti-inflammatory, antioxidative stress, and regenerative properties. MSCs are regulated by mitochondrial function, as well as oxidant stress responses. Maintaining mitochondrial homeostasis will likely be key for MSCs to stimulate proper lung development and regeneration in Bronchopulmonary dysplasia. In recent years, MSCs have demonstrated promising results in treating and preventing bronchopulmonary dysplasia. Studies have shown that MSC therapy can reduce inflammation, mitochondrial impairment, lung injury, and fibrosis. In light of this, MSCs have emerged as a potential therapeutic option for treating Bronchopulmonary dysplasia. The article explores the role of MSCs in lung development and disease, summarizes MSC therapy’s effectiveness in treating Bronchopulmonary dysplasia, and delves into the mechanisms behind this treatment. Frontiers Media S.A. 2023-10-30 /pmc/articles/PMC10642488/ /pubmed/37965579 http://dx.doi.org/10.3389/fcell.2023.1247339 Text en Copyright © 2023 Zhang, Mulder, Riddle, Song and Yue. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Zhang, Shuqing Mulder, Cassidy Riddle, Suzette Song, Rui Yue, Dongmei Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title | Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title_full | Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title_fullStr | Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title_full_unstemmed | Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title_short | Mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
title_sort | mesenchymal stromal/stem cells and bronchopulmonary dysplasia |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642488/ https://www.ncbi.nlm.nih.gov/pubmed/37965579 http://dx.doi.org/10.3389/fcell.2023.1247339 |
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