Consequences of early postnatal lipopolysaccharide exposure on developing lungs in mice

• Published in: American journal of physiology. Lung cellular and molecular physiology Vol. 316; no. 1; pp. L229 - L244
• Main Authors: Shrestha, Amrit Kumar, Bettini, Matthew L, Menon, Renuka T, Gopal, Vashisht Y N, Huang, Shixia, Edwards, Dean P, Pammi, Mohan, Barrios, Roberto, Shivanna, Binoy
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.01.2019
• Subjects: Alveoli; Animals; Animals, Newborn; Apoptosis; Cell proliferation; Cell Proliferation - drug effects; Dosage; Dose-Response Relationship, Drug; Dysplasia; Exposure; Flow cytometry; Genomic analysis; Growth rate; Hypotheses; Infants; Inflammation; Inflammation - chemically induced; Inflammation - metabolism; Inflammation - pathology; Lipopolysaccharides; Lipopolysaccharides - toxicity; Lung diseases; Lungs; Macrophages; Mice; Protein expression; Proteins; Proteomics; Pulmonary Alveoli - growth & development; Pulmonary Alveoli - metabolism; Pulmonary Alveoli - pathology; Rodents; Saccule; Sepsis; T-Lymphocytes, Regulatory - metabolism; T-Lymphocytes, Regulatory - pathology; Therapeutic applications; T-regulatory cells; proteomics; bronchopulmonary dysplasia; lipopolysaccharide; inflammation
• ISSN: 1040-0605; 1522-1504
• DOI: 10.1152/ajplung.00560.2017

Bronchopulmonary dysplasia (BPD) is a chronic lung disease of infants that is characterized by interrupted lung development. Postnatal sepsis causes BPD, yet the contributory mechanisms are unclear. To address this gap, studies have used lipopolysaccharide (LPS) during the alveolar phase of lung development. However, the lungs of infants who develop BPD are still in the saccular phase of development, and the effects of LPS during this phase are poorly characterized. We hypothesized that chronic LPS exposure during the saccular phase disrupts lung development by mechanisms that promote inflammation and prevent optimal lung development and repair. Wild-type C57BL6J mice were intraperitoneally administered 3, 6, or 10 mg/kg of LPS or a vehicle once daily on postnatal days (PNDs) 3-5. The lungs were collected for proteomic and genomic analyses and flow cytometric detection on PND6. The impact of LPS on lung development, cell proliferation, and apoptosis was determined on PND7. Finally, we determined differences in the LPS effects between the saccular and alveolar lungs. LPS decreased the survival and growth rate and lung development in a dose-dependent manner. These effects were associated with a decreased expression of proteins regulating cell proliferation and differentiation and increased expression of those mediating inflammation. While the lung macrophage population of LPS-treated mice increased, the T-regulatory cell population decreased. Furthermore, LPS-induced inflammatory and apoptotic response and interruption of cell proliferation and alveolarization was greater in alveolar than in saccular lungs. Collectively, the data support our hypothesis and reveal several potential therapeutic targets for sepsis-mediated BPD in infants.