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...

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Main Authors: Shuqing Zhang, Cassidy Mulder, Suzette Riddle, Rui Song, Dongmei Yue
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-10-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2023.1247339/full
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author Shuqing Zhang
Cassidy Mulder
Suzette Riddle
Rui Song
Dongmei Yue
author_facet Shuqing Zhang
Cassidy Mulder
Suzette Riddle
Rui Song
Dongmei Yue
author_sort Shuqing Zhang
collection DOAJ
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.
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spelling doaj.art-169f50ad18704e89a26094f1b7da107f2023-10-30T09:22:52ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2023-10-011110.3389/fcell.2023.12473391247339Mesenchymal stromal/stem cells and bronchopulmonary dysplasiaShuqing Zhang0Cassidy Mulder1Suzette Riddle2Rui Song3Dongmei Yue4School of Pharmacy, China Medical University, Shenyang, ChinaLiberty University College of Osteopathic Medicine, Lynchburg, VA, United StatesCardiovascular Pulmonary Research Laboratories, Departments of Pediatrics and Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United StatesLawrence D. Longo, MD Center for Perinatal Biology, Department of Basic Sciences, Loma Linda University School of Medicine, Loma Linda, CA, United StatesDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, ChinaBronchopulmonary 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.https://www.frontiersin.org/articles/10.3389/fcell.2023.1247339/fullstem cellsbronchopulmonary dysplasiadevelopmentextracellular vesiclesmitochondria
spellingShingle Shuqing Zhang
Cassidy Mulder
Suzette Riddle
Rui Song
Dongmei Yue
Mesenchymal stromal/stem cells and bronchopulmonary dysplasia
Frontiers in Cell and Developmental Biology
stem cells
bronchopulmonary dysplasia
development
extracellular vesicles
mitochondria
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 stem cells
bronchopulmonary dysplasia
development
extracellular vesicles
mitochondria
url https://www.frontiersin.org/articles/10.3389/fcell.2023.1247339/full
work_keys_str_mv AT shuqingzhang mesenchymalstromalstemcellsandbronchopulmonarydysplasia
AT cassidymulder mesenchymalstromalstemcellsandbronchopulmonarydysplasia
AT suzetteriddle mesenchymalstromalstemcellsandbronchopulmonarydysplasia
AT ruisong mesenchymalstromalstemcellsandbronchopulmonarydysplasia
AT dongmeiyue mesenchymalstromalstemcellsandbronchopulmonarydysplasia