S100A8 Chemotactic Protein Is Abundantly Increased, but Only a Minor Contributor to LPS-Induced, Steroid Resistant Neutrophilic Lung Inflammation in Vivo

Lipopolysaccharides Male Proteomics 0301 basic medicine 570 Proteome Neutrophils Drug Resistance Airway Inflammation 610 Biochemical Research Methods Dexamethasone Exacerbations 730110 Respiratory system and diseases (incl. asthma) Mice 03 medical and health sciences Medical Biochemistry: Proteins and Peptides Cystic-fibrosis Animals Calgranulin A Electrophoresis, Gel, Two-Dimensional Lung Glucocorticoids Macrophage Expression Inflammation Mice, Inbred BALB C Chemotaxis S100 Proteins Cp-10 Pneumonia Innate Immunity 3. Good health Gene Expression Regulation Obstructive Pulmonary-disease Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization 320299 Immunology not elsewhere classified Endocrine Organs and Diseases (incl. Diabetes) Colony-stimulating Factor Severe Asthma Factor-kappa-b
DOI: 10.1021/pr049829t Publication Date: 2005-02-14T05:43:50Z
ABSTRACT
Neutrophilic lung inflammation is an essential component of host defense against diverse eukaryotic and prokaryotic pathogens, but in chronic inflammatory lung diseases, such as chronic obstructive lung disease (COPD), severe asthma, cystic fibrosis, and bronchiolitis, it may damage the host. Glucocorticosteroids are widely used in these conditions and in their infectious exacerbations; however, the clinical efficacy of steroids is disputed. In this study, we used a proteomic approach to identify molecules contributing to neutrophilic inflammation induced by transnasal administration of lipopolysaccharide (LPS) that were also resistant to the potent glucocorticosteroid dexamethasone (Dex). We confirmed that Dex was biologically active at both the transcript (suppression of GM-CSF and TNFalphatranscripts) and protein levels (induction of lipocortin) and used 2D-PAGE/MALDI-TOF to generate global expression profiles, identifying six LPS-induced proteins that were Dex resistant. Of these, S100A8, a candidate neutrophil chemotactic factor, was profiled in detail. Steroid refractory S100A8 expression was highly abundant, transcriptionally regulated, secreted into lung lavage fluid and immunohistochemically localized to tissue infiltrating neutrophils. However, in marked contrast to other vascular beds, neutralizing antibodies to S100A8 had only a weak anti-neutrophil recruitment effect and antibodies against the related S100A9 were ineffective. These data highlight the need for extensive in vivo profiling of proteomically identified candidate molecules and demonstrates that S100A8, despite its abundance, resistance to steroids and known chemotactic activity, is unlikely to be an important determinant of LPS-induced neutrophilic lung inflammation in vivo.
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