| Literature DB >> 19322781 |
Florence Quesada Calvo1, Marianne Fillet, Dominique de Seny, Marie-Alice Meuwis, Raphael Maree, Céline Crahay, Geneviève Paulissen, Natacha Rocks, Maud Gueders, Louis Wehenkel, Marie-Paule Merville, Renaud Louis, Jean-Michel Foidart, Agnes Noël, Didier Cataldo.
Abstract
Asthma is a complex inflammatory disease of airways. A network of reciprocal interactions between inflammatory cells, peptidic mediators, extracellular matrix components, and proteases is thought to be involved in the installation and maintenance of asthma-related airway inflammation and remodeling. To date, new proteic mediators displaying significant activity in the pathophysiology of asthma are still to be unveiled. The main objective of this study was to uncover potential target proteins by using surface-enhanced laser desorption/ionization-time of flight-mass spectrometry (SELDI-TOF-MS) on lung samples from mouse models of allergen-induced airway inflammation and remodeling. In this model, we pointed out several protein or peptide peaks that were preferentially expressed in diseased mice as compared to controls. We report the identification of different five proteins: found inflammatory zone 1 or RELM alpha (FIZZ-1), calcyclin (S100A6), clara cell secretory protein 10 (CC10), Ubiquitin, and Histone H4.Entities:
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Year: 2009 PMID: 19322781 DOI: 10.1002/pmic.200800643
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984