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          Institute: MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut)     Collection: Yearbook_2014     Display Documents



ID: 682133.0, MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut) / Yearbook_2014
Cofilin, a hypoxia-regulated protein in murine lungs identified by 2DE: role of the cytoskeletal protein cofilin in pulmonary hypertension
Authors:Veith, C.; Schmitt, S.; Veit, F.; Dahal, B. K.; Wilhelm, J.; Klepetko, W.; Marta, G.; Seeger, W.; Schermuly, R. T.; Grimminger, F.; Ghofrani, H. A.; Fink, L.; Weissmann, N.; Kwapiszewska, G.
Date of Publication (YYYY-MM-DD):2013-01
Journal Abbrev.:Proteomics
Volume:13
Issue / Number:1
Start Page:75
End Page:88
Audience:Not Specified
Abstract / Description:Chronic alveolar hypoxia induces vascular remodeling processes in the lung resulting in pulmonary hypertension (PH). However, the mechanisms underlying pulmonary remodeling processes are not fully resolved yet. To investigate functional changes occurring during hypoxia exposure we applied 2DE to compare protein expression in lungs from mice subjected to 3 h of alveolar hypoxia and those kept under normoxic conditions. Already after this short-time period several proteins were significantly regulated. Subsequent analysis by MALDI-MS identified cofilin as one of the most prominently upregulated proteins. The regulation was confirmed by western blotting and its cellular localization was determined by immunohisto- and immunocytochemistry. Interestingly, enhanced cofilin serine 3 phosphorylation was observed after short-term and after chronic hypoxia-induced PH in mice, in pulmonary arterial smooth muscle cells (PASMC) from monocrotaline-induced PH in rats, in lungs of idiopathic pulmonary arterial hypertension patients and in hypoxic or platelet-derived growth factor BB-treated human PASMC. Furthermore, elevated cofilin phosphorylation was attenuated by curative treatment of monocrotaline-induced PH in rats and hypoxia-induced PH in mice with the PDGF-BB receptor antagonist imatinib. In conclusion, short-term hypoxic exposure induced prominent changes in lung protein regulation. These very early changes allowed us to identify potential triggers of PH. Thus, respective 2DE analysis can lead to the identification of new target proteins for the possible treatment of PH.
Free Keywords:*Actin Depolymerizing Factors/genetics/metabolism; Animals; Anoxia/metabolism; Cell Proliferation; Gene Expression Regulation; Humans; *Hypertension, Pulmonary/genetics/metabolism/pathology; *Lung/metabolism/physiopathology; Male; Mice; Myocytes, Smooth Muscle/cytology/metabolism; Phosphorylation; *Proteins/genetics/metabolism; Proto-Oncogene Proteins c-sis/administration & dosage; Pulmonary Artery/cytology/metabolism; Rats; Signal Transduction/genetics; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Up-Regulation
External Publication Status:published
Document Type:Article
Communicated by:Svea Hümmer
Affiliations:MPI für physiologische und klinische Forschung
Identifiers:ISSN:1615-9861 (Electronic) 1615-9853 (Linking) %R 10.1002/pmic.201200206
URL:http://www.ncbi.nlm.nih.gov/pubmed/23161571
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