Mesenchymal Stem Cell-derived Type II Alveolar Epithelial Progenitor Cells Attenuate LPS-induced Acute Lung Injury and Reduce P63 Expression
- Authors: Ma N.1, Zhang M.1, Xu G.2, Zhang L.3, Luo M.1, Luo M.1, Wang X.1, Tang H.1, Wang X.1, Liu L.4, Zhong X.5, Feng J.4, Li Y.1
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Affiliations:
- Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
- Inflammation & Allergic Diseases Research Uni, The Affiliated Hospital of Southwest Medical University
- Department of Neurosurgery, The Affiliated Hospital of Southwest Medical University
- Laboratory of Anesthesiology, Southwest Medical University
- Department of Gastroenterology, The Affiliated Hospital of Southwest Medical University
- Issue: Vol 19, No 2 (2024)
- Pages: 245-256
- Section: Medicine
- URL: https://snv63.ru/1574-888X/article/view/645716
- DOI: https://doi.org/10.2174/1574888X18666230501234836
- ID: 645716
Cite item
Full Text
Abstract
Aim:Acute respiratory distress syndrome (ARDS)/acute lung injury (ALI) is a severe clinical respiratory-failure disease mainly characterized by acute damage to the alveolar epithelium and pulmonary vascular endothelial cells. Stem cell therapy has emerged as a potential regenerative strategy for ARDS/ALI, however, the outcome is limited, and the underlying mechanisms are unclear.
Introduction:We established a differentiation system for bone marrow-derived mesenchymal stem cellderived (BM-MSC) type II alveolar epithelial progenitor cells (AECIIs) and assessed their regulatory effects on lipopolysaccharide (LPS)-induced ALI.
Methods:We induced BM-MSC differentiation into AECIIs using a specific conditioned medium. After 26 days of differentiation, 3×105 BM-MSC-AECIIs were used to treat mice with LPS-induced ALI through tracheal injection.
Results:After tracheal injection, BM-MSC-AECIIs migrated to the perialveolar area and reduced LPSinduced lung inflammation and pathological injury. RNA-seq suggested that P63 protein was involved in the effects of BM-MSC-AECIIs on lung inflammation.
Conclusion:Our results suggest that BM-MSC-AECIIs may reduce LPS-induced acute lung injury by decreasing P63 expression.
About the authors
Ning Ma
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Mengwei Zhang
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Guofeng Xu
Inflammation & Allergic Diseases Research Uni, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Lifang Zhang
Department of Neurosurgery, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Min Luo
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Meihua Luo
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Xing Wang
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Hongmei Tang
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Xiaoyun Wang
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Li Liu
Laboratory of Anesthesiology, Southwest Medical University
Email: info@benthamscience.net
Xiaolin Zhong
Department of Gastroenterology, The Affiliated Hospital of Southwest Medical University
Email: info@benthamscience.net
Jianguo Feng
Laboratory of Anesthesiology, Southwest Medical University
Email: info@benthamscience.net
Yuying Li
Inflammation & Allergic Diseases Research Unit, The Affiliated Hospital of Southwest Medical University
Author for correspondence.
Email: info@benthamscience.net
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