Lung Mesenchymal Stem Cells Ameliorate Elastase-Induced Damage in an Animal Model of Emphysema
Autor: | Antonella De Angelis, Donato Cappetta, Gioia Tartaglione, Loreta Pia Ciuffreda, Francesco Rossi, Giuseppe Spaziano, Bruno D'Agostino, Angela Liparulo, Liberato Berrino, Konrad Urbanek, Grazia Esposito, Manuela Sgambato, Elena Piegari, Teresa Russo |
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Přispěvatelé: | Cappetta, Donato, De Angelis, Antonella, Spaziano, Giuseppe, Tartaglione, Gioia, Piegari, Elena, Esposito, Grazia, Ciuffreda, Loreta Pia, Liparulo, Angela, Sgambato, Manuela, Russo, Teresa Palmira, Rossi, Francesco, Berrino, Liberato, Urbanek, Konrad, D’Agostino, Bruno, Cappetta, D, De Angelis, A, Spaziano, G, Tartaglione, G, Piegari, E, Esposito, G, Ciuffreda, Lp, Liparulo, A, Sgambato, M, Russo, Tp, Rossi, F, Berrino, L, Urbanek, K, D'Agostino, B |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
lcsh:Internal medicine Pathology medicine.medical_specialty Article Subject Pulmonary function testing 03 medical and health sciences Paracrine signalling medicine Respiratory system lcsh:RC31-1245 Molecular Biology Lung business.industry Elastase Mesenchymal stem cell Cell Biology respiratory system Pathophysiology respiratory tract diseases 030104 developmental biology medicine.anatomical_structure Hepatocyte growth factor business Research Article medicine.drug |
Zdroj: | Stem Cells International, Vol 2018 (2018) Stem Cells International |
ISSN: | 1687-9678 1687-966X |
DOI: | 10.1155/2018/9492038 |
Popis: | This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Pulmonary emphysema is a respiratory condition characterized by alveolar destruction that leads to airflow limitation and reduced lung function. Although with extensive research, the pathophysiology of emphysema is poorly understood and effective treatments are still missing. Evidence suggests that mesenchymal stem cells (MSCs) possess the ability to engraft the injured tissues and induce repair via a paracrine effect. Thus, the aim of this study was to test the effects of the intratracheal administration of lung-derived mouse MSCs in a model of elastase-induced emphysema. Pulmonary function (static lung compliance) showed an increased stiffness induced by elastase, while morphometric findings (mean linear intercept and tissue/alveolar area) confirmed the severity of alveolar disruption. Contrarily, MSC administration partially restored lung elasticity and alveolar architecture. In the absence of evidence that MSCs acquired epithelial phenotype, we detected an increased proliferative activity of aquaporin 5-and surfactant protein C-positive lung cells, suggesting MSC-driven paracrine mechanisms. The data indicate the mediation of hepatocyte growth factor in amplifying MSC-driven tissue response after injury. Our study shed light on supportive properties of lung-derived MSCs, although the full identification of mechanisms orchestrated by MSCs and responsible for epithelial repair after injury is a critical aspect yet to be achieved. Copyright © 2018 Donato Cappetta et al. Pulmonary emphysema is a respiratory condition characterized by alveolar destruction that leads to airflow limitation and reduced lung function. Although with extensive research, the pathophysiology of emphysema is poorly understood and effective treatments are still missing. Evidence suggests that mesenchymal stem cells (MSCs) possess the ability to engraft the injured tissues and induce repair via a paracrine effect. Thus, the aim of this study was to test the effects of the intratracheal administration of lung-derived mouse MSCs in a model of elastase-induced emphysema. Pulmonary function (static lung compliance) showed an increased stiffness induced by elastase, while morphometric findings (mean linear intercept and tissue/alveolar area) confirmed the severity of alveolar disruption. Contrarily, MSC administration partially restored lung elasticity and alveolar architecture. In the absence of evidence that MSCs acquired epithelial phenotype, we detected an increased proliferative activity of aquaporin 5- and surfactant protein C-positive lung cells, suggesting MSC-driven paracrine mechanisms. The data indicate the mediation of hepatocyte growth factor in amplifying MSC-driven tissue response after injury. Our study shed light on supportive properties of lung-derived MSCs, although the full identification of mechanisms orchestrated by MSCs and responsible for epithelial repair after injury is a critical aspect yet to be achieved. |
Databáze: | OpenAIRE |
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