Angiogenesis is essential in development and wound healing and contributes to the pathogenesis of many diseases. The signalling pathways activated in angiogenesis are, in part, known and the overall tyrosine phosphorylation of cellular proteins plays a relevant role. By RNA fingerprinting, we isolated a tyrosine phosphatase, HD-PTP, modulated in human endothelial cells exposed to human immunodeficiency virus type 1 Tat, a viral protein known to be angiogenic. For the first time, we describe HD-PTP at the protein level. HD-PTP, a 185 kDa cytosolic protein which is expressed in endothelial cells of different origin. We show that HD-PTP is upregulated by Tat at the mRNA but not at the protein level. HD-PTP protein is differentially modulated by two angiogenic growth factors. While Vascular Endothelial Growth Factor does not affect protein levels, Fibroblast Growth Factor-2 induces HD-PTP degradation via the proteasome system.
|Titolo:||The tyrosine phosphatase HD-PTP is regulated by FGF-2 through proteasome degradation|
|Parole Chiave:||Angiogenesis; Fibroblast Growth Factor; HD-PTP; HIV-1-Tat; Proteasome; Vascular Endothelial Growth Factor; Vessel|
|Settore Scientifico Disciplinare:||Settore MED/04 - Patologia Generale|
|Data di pubblicazione:||1-set-2006|
|Digital Object Identifier (DOI):||10.2741/1956|
|Appare nelle tipologie:||01 - Articolo su periodico|