Preclinical evaluation of human secretoglobin 3A2 in mouse models of lung development and fibrosis
Autor: | Aprile L. Pilon, Melissa E Winn, Yan Cai, Shioko Kimura, William K. Gillette, Jacek Lubkowski, John K. Zehmer |
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Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
Pulmonary and Respiratory Medicine
Physiology Phospholipase A2 Inhibitors medicine.medical_treatment Pulmonary Fibrosis Drug Evaluation Preclinical Biological Availability Biology Bleomycin Secretoglobins Tissue Culture Techniques chemistry.chemical_compound Mice Fibrosis In vivo Physiology (medical) Placenta Pulmonary fibrosis medicine Animals Humans Lung Growth factor Gene Expression Regulation Developmental Cell Biology medicine.disease Recombinant Proteins Mice Inbred C57BL Phospholipases A2 medicine.anatomical_structure chemistry Immunology Cancer research Call for Papers Female Ex vivo |
Popis: | Secretoglobin (SCGB) 3A2 is a member of the SCGB gene superfamily of small secreted proteins, predominantly expressed in lung airways. We hypothesize that human SCGB3A2 may exhibit anti-inflammatory, growth factor, and antifibrotic activities and be of clinical utility. Recombinant human SCGB3A2 was expressed, purified, and biochemically characterized as a first step to its development as a therapeutic agent in clinical settings. Human SCGB3A2, as well as mouse SCGB3A2, readily formed a dimer in solution and exhibited novel phospholipase A2 inhibitory activity. This is the first demonstration of any quantitative biochemical measurement for the evaluation of SCGB3A2 protein. In the mouse as an experimental animal, human SCGB3A2 exhibited growth factor activity by promoting embryonic lung development in both ex vivo and in vivo systems and antifibrotic activity in the bleomycin-induced lung fibrosis model. The results suggested that human SCGB3A2 can function as a growth factor and an antifibrotic agent in humans. When SCGB3A2 was administered to pregnant female mice through the tail vein, the protein was detected in the dam's serum and lung, as well as the placenta, amniotic fluids, and embryonic lungs at 10 min postadministration, suggesting that SCGB3A2 readily crosses the placenta. The results warrant further development of recombinant SCGB3A2 as a therapeutic agent in treating patients suffering from lung diseases or preterm infants with respiratory distress. |
Databáze: | OpenAIRE |
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