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Role of beta1-integrins for G protein-coupled signaling cascades

Subject Area Dermatology
Term from 2002 to 2008
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 5394286
 
Aim of the proposal is to elucidate the role of b1-integrins for pertussis toxin-sensitive G protein-coupled signaling pathways. The key finding motivating this investigation is a selective muscarinic signaling defect in b1 integrin (-/-) cardiomyocytes due to displacement of Gi. The relevance of this defect will be investigated in endothelial cells, where Gi-coupled signaling represents a key event for endothelial cell function. We are planning to analyze functional coupling of the other pertussis toxin sensitive G protein Go in ES cell-derived neuronal cells. To understand the significance of the cytoskeletal integrity for Gi/o signaling, reconstitution experiments will be performed, where G protein subunits are reintroduced into the cytosol via the patch pipette and recovery of function tested in b1 integrin (-/-) ES cell-derived cells. The significance of intact extracellular anchorage for G protein-coupled signaling is evaluated in b1 integrin (-/-) cells, where addition of laminin rescues defective basal membrane formation. The proposed study is aimed to clarify the molecular role of b1 integrins in membrane delimited signal transduction processes.
DFG Programme Priority Programmes
Participating Person Professor Dr. Bernd Fleischmann
 
 

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