VEGFR and Type-V RTK Activation and Signaling

Vascular endothelial growth factor receptors (VEGFRs) in vertebrates play essential roles in the regulation of angiogenesis and lymphangiogenesis. VEGFRs belong to the receptor-type tyrosine kinase (RTK) supergene family. They consist of a ligand-binding region with seven immunoglobulin (7 Ig)-like domains, a trans-membrane (TM) domain, and a tyrosine kinase (TK) domainwith a long kinase insert (KI) (also known as a type-V RTK). Structurally, VEGFRs are distantly related to the members of the M-colony stimulating factor receptor/platelet-derived growth factor receptor (CSFR)/(PDGFR) family, which have five immunoglobulin (5 Ig)-like domains. However, signal transduction in VEGFRs significantly differs from that in M-CSFR/PDGFRs. VEGFR2, the major signal transducer for angiogenesis, preferentially uses the phospholipaseCg-protein kinaseC (PLC-g-PKC)-MAPKpathway,whereasM-CSFR/ PDGFRs use the PI3 kinase-Ras-MAPK pathway for cell proliferation. In phylogenetic de-velopment, the VEGFR-like receptor in nonvertebrates appears to be the ancestor of the 7 Ig-and 5 Ig-RTK families because most nonvertebrates have only a single 7 Ig-RTK gene. In mammals, VEGFRs are deeply involved in pathological angiogenesis, including cancer and inflammation. Thus, an efficient inhibitor targeting VEGFRs could be useful in suppressin