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Inhibition of Rac1 GTPase downregulates vascular endothelial growth factor receptor‐2 expression by suppressing Sp1‐dependent DNA binding in human endothelial cells
Author(s) -
Meissner Markus,
Michailidou Despina,
Stein Monika,
Hrgovic Igor,
Kaufmann Roland,
Gille Jens
Publication year - 2009
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2009.00867.x
Subject(s) - rac1 , microbiology and biotechnology , rhoa , biology , cdc42 , small gtpase , angiogenesis , sp1 transcription factor , transcription factor , kinase insert domain receptor , signal transduction , cancer research , chemistry , vascular endothelial growth factor a , gene expression , vascular endothelial growth factor , promoter , gene , biochemistry , vegf receptors
RhoA, Rac1 and CDC42 are small GTP‐binding proteins of the Rho family that play a crucial role in regulation of the actin‐based cytoskeleton. In addition to cell growth regulation, they are implicated in transcriptional activation, oncogenic transformation and angiogenesis. The small Rho‐GTPases have been linked to vascular endothelial growth factor (VEGF)‐induced signalling pathways, but their role has not yet been elucidated. As signalling via the VEGF receptor‐2 (VEGFR2) pathway is critical for angiogenic responses in cancer, wound repair and ischaemic and inflammatory diseases, we investigated whether the small Rho‐GTPase Rac1 influences VEGFR2 expression in human endothelial cells. In this study, we show that a dominant negative Rac1 expression vector led to a pronounced decrease in VEGFR2 mRNA and protein expression. To identify minimal promoter requirements and potential applications of the small Rho‐GTPases, we used VEGFR2 promoter–reporter gene constructs containing various deletions. The inhibitory effects of dominant negative Rac1 on the transcriptional activity of the VEGFR2 promoter localized to an element between −77 and −60 that contains an Sp1 transcription factor binding site. Electrophoretic mobility shift assays demonstrated that constitutive Sp1‐dependent DNA binding decreased with Rac1 inhibition. Hence, repression of the small Rho GTPase Rac1 seems to be an additional critical molecular mechanism in the regulation of VEGFR2 expression.