Modulation of Pulmonary Fibrosis by Pulmonary Surfactant-Associated Phosphatidylethanolamine In Vitro and In Vivo

Pulmonary fibrosis (PF) is characterized by excessive collagen deposition and impaired lung function. Pulmonary surfactant may modulate fibroblast activity and offer therapeutic benefits. We developed a natural porcine pulmonary surfactant (NPPS) enriched with 1,2-dipalmitoyl-rac-glycero-3-phosphatidylethanolamine (PE) and evaluated its biophysical and biological properties. Biophysical analysis showed that PE improved surfactant performance by increasing surface pressure and stability. In vitro, NPPS-PE reduced collagen expression and induced apoptosis in normal human lung fibroblasts; in addition, it decreased proliferation in fibroblasts stimulated with TGF-β. In vivo, NPPS-PE improved gas exchange and significantly reduced collagen deposition in bleomycin-treated mice. These findings suggest that NPPS-PE may be a promising therapeutic strategy for fibrosing lung diseases.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-07-24
DOI
https://doi.org/10.3390/ijms26157132
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00

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article

Modulation of Pulmonary Fibrosis by Pulmonary Surfactant-Associated Phosphatidylethanolamine In Vitro and In Vivo

David A. Contreras‐Cruz, María Guadalupe Hernández-Linares, Beatriz Tlatelpa-Romero, Gabriel Guerrero‐Luna et al.
1 links
International Journal of Molecular Sciences
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Modulation of Pulmonary Fibrosis by Pulmonary Surfactant-Associated Phosphatidylethanolamine In Vitro and In Vivo

David A. Contreras‐Cruz, María Guadalupe Hernández-Linares, Beatriz Tlatelpa-Romero, Gabriel Guerrero‐Luna, Sinuhé Ruiz-Salgado, Jesús Pérez‐Gil, Criselda Mendoza-Milla, Roberto Berra‐Romani, Amaya Blanco-Rivero, Bárbara Olmeda, María Pérez-Fernández, René de-la-Rosa Paredes, Olga Cañadas, Yair Romero, Alonso Antonio Collantes-Gutiérrez, Luis G. Vázquez-de-Lara Cisneros, José Luis Martinez-Vaquero
article en

Abstract

Pulmonary fibrosis (PF) is characterized by excessive collagen deposition and impaired lung function. Pulmonary surfactant may modulate fibroblast activity and offer therapeutic benefits. We developed a natural porcine pulmonary surfactant (NPPS) enriched with 1,2-dipalmitoyl-rac-glycero-3-phosphatidylethanolamine (PE) and evaluated its biophysical and biological properties. Biophysical analysis showed that PE improved surfactant performance by increasing surface pressure and stability. In vitro, NPPS-PE reduced collagen expression and induced apoptosis in normal human lung fibroblasts; in addition, it decreased proliferation in fibroblasts stimulated with TGF-β. In vivo, NPPS-PE improved gas exchange and significantly reduced collagen deposition in bleomycin-treated mice. These findings suggest that NPPS-PE may be a promising therapeutic strategy for fibrosing lung diseases.

International Journal of Molecular SciencesVol. 26(15)
Universidad Autónoma del Estado de Hidalgo (MX), Universidad Complutense de Madrid (ES), Universidad Autónoma de la Ciudad de México (MX), Hospital General de México (MX), Research Institute Hospital 12 de Octubre (ES), Instituto Nacional de Enfermedades Respiratorias (MX), Instituto Universitario Puebla (MX), Instituto de Química y Fisicoquímica Biológicas (AR), Benemérita Universidad Autónoma de Puebla (MX), Universidad Nacional Autónoma de México (MX)
Ministerio de Ciencia e Innovación
Openalex Percentile: Top 72%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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