Urokinase-type Plasminogen Activator (uPA) Promotes Angiogenesis by Attenuating Proline-rich Homeodomain Protein (PRH) Transcription Factor Activity and De-repressing Vascular Endothelial Growth Factor (VEGF) Receptor Expression

作者：Stepanova Victoria^*; Jayaraman Padma Sheela; Zaitsev Sergei V; Lebedeva Tatiana; Bdeir Khalil; Kershaw Rachael; Holman Kelci R; Parfyonova Yelena V; Semina Ekaterina V; Beloglazova Irina B; Tkachuk Vsevolod A; Cines Douglas B

来源：Journal of Biological Chemistry, 2016, 291(29): 15029-15045.

DOI：10.1074/jbc.M115.78490

Urokinase-type plasminogen activator (uPA) regulates angiogenesis and vascular permeability through proteolytic degradation of extracellular matrix and intracellular signaling initiated upon its binding to uPAR/CD87 and other cell surface receptors, Here, we describe an additional mechanism by which uPA regulates angiogenesis. Ex vivo VEGF-induced vascular sprouting from Matrigel-embedded aortic rings isolated from uPA knock -out (uPA-1) mice was impaired compared with vessels emanating from wild -type mice. Endothelial cells isolated from uPA' mice show less proliferation and migration in response to VEGF than their wild type counterparts or uPA endothelial cells in which expression of wild type uPA had been restored. We reported previously that uPA is transported from cell surface receptors to nuclei through a mechanism that requires its kringle domain. Intranuclear uPA modulates gene transcription by binding to a subset of transcription factors. Here we report that wild type single-chain uPA, but not uPA variants incapable of nuclear transport, increases the expression of cell surface VEGF receptor 1 (VEGFR1) and VEGF receptor 2 (VEGFR2) by translocating to the nuclei of ECs. Intranuclear single-chain uPA binds directly to and interferes with the function of the transcription factor hematopoietically expressed homeodomain protein or proline-rich homeodomain protein (HHEX/PRH), which thereby lose their physiologic capacity to repress the activity of vehgrl and vegfr2 gene promoters. These studies identify uPA-dependent de -repression of vegfr1 and vegfr2 gene transcription through binding to HHEX/PRH as a novel mechanism by which uPA mediates the pro-angiogenic effects of VEGE and identifies a potential new target for control of pathologic angiogenesis.

• 出版日期2016-7-15