Localization and functional characterization of pulmonary bovine odorant-binding protein.

Abstract

Bovine odorant-binding protein (OBP) may function in olfaction and defense against oxidative injury, but its role in inflammation and defense against bacterial infection has not been investigated. Expression of OBP was discovered in the bovine lung and found to undergo changes in abundance during glucocorticoid administration and stress. OBP was localized to nasal, tracheal, and bronchial mucosal glands with immunohistochemistry, with faint expression in airway surface epithelium and none in bronchioles or alveoli. Two isoforms of OBP were identified, appearing to be differentially regulated during lipopolysaccharide-induced pulmonary inflammation, but differences between these isoforms were not revealed by matrix-assisted laser desorption/ionization-time of flight mass spectrometry. Functional studies showed no effect of OBP on in vitro growth of Escherichia coli or Mannheimia haemolytica under iron-replete or iron-depleted conditions, nor did OBP opsonize bacteria for an enhanced neutrophil oxidative burst. However, OBP did reduce the ability of supernatants from lipopolysaccharide-stimulated macrophages to induce neutrophil chemotaxis. These findings indicate that OBP may inhibit neutrophil recruitment by inflammatory mediators, and they suggest an ability to bind macrophage-derived inflammatory mediators within the airways.

• Authors: G B Mitchell, M E Clark, R Lu, J L Caswell
• Journal: Veterinary pathology (Vet Pathol) Vol. 48 Issue 6 Pg. 1054-60 (Nov 2011) ISSN: 1544-2217 [Electronic] United States
• PMID: 20826843 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Glucocorticoids
• Lipopolysaccharides
• Protein Isoforms
• Receptors, Odorant
• Recombinant Proteins
• odorant-binding protein

Topics

• Amino Acid Sequence
• Animals
• Bronchoalveolar Lavage Fluid (chemistry, immunology)
• Cattle
• Chemotaxis (drug effects)
• Escherichia coli (growth & development, immunology)
• Gene Expression Regulation (immunology)
• Glucocorticoids (administration & dosage)
• Inflammation (veterinary)
• Lipopolysaccharides (pharmacology)
• Lung (metabolism)
• Macrophages (metabolism)
• Mannheimia haemolytica (growth & development, immunology)
• Molecular Sequence Data
• Nasal Mucosa (metabolism)
• Neutrophil Infiltration (drug effects, immunology)
• Neutrophils (drug effects, metabolism)
• Oxidative Stress
• Protein Isoforms
• Rabbits
• Receptors, Odorant (chemistry, immunology, metabolism)
• Recombinant Proteins
• Trachea (metabolism)