PAX2 expression by HHV-8-infected endothelial cells induced a proangiogenic and proinvasive phenotype

Blood. 2008 Mar 1;111(5):2806-15. doi: 10.1182/blood-2007-04-085555. Epub 2007 Dec 3.

Abstract

In the present study, we evaluated whether infection of microvascular endothelial cells (HMECs) with HHV-8 can trigger the expression of PAX2 oncogene and whether PAX2 protein is involved in HHV-8-induced transformation of HMECs. We found that HHV-8 infection induced the expression of both the PAX2 gene and PAX2 protein in HMECs but failed to induce PAX2 protein in HMECs stably transfected with PAX2 antisense (HMEC-AS). HHV-8-infected HMECs but not HMEC-AS acquired proinvasive proadhesive properties, enhanced survival and in vitro angiogenesis, suggesting a correlation between PAX2 expression and the effects triggered by HHV-8 infection. When HMEC-expressing PAX2 by stable transfection with PAX2 sense gene or by HHV-8 infection were implanted in vivo in severe combined immunodeficient (SCID) mice, enhanced angiogenesis and proliferative lesions resembling KS were observed. HHV-8-infected HMEC-AS failed to induce angiogenesis and KS-like lesions. These results suggest that the expression of PAX2 is required for the proangiogenic and proinvasive changes induced by HHV-8 infection in HMECs. In conclusion, HHV-8 infection may activate an embryonic angiogenic program in HMECs by inducing the expression of PAX2 oncogene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Adhesion
  • Cell Movement
  • Cells, Cultured
  • Chemokine CCL2 / metabolism
  • Collagen
  • Drug Combinations
  • Endothelial Cells / enzymology
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology*
  • Endothelial Cells / virology*
  • Enzyme Activation
  • Gene Expression Regulation
  • Herpesvirus 8, Human / physiology*
  • Intercellular Adhesion Molecule-1 / metabolism
  • Laminin
  • Leukocytes / cytology
  • Mice
  • Mice, SCID
  • Neoplasm Invasiveness
  • Neovascularization, Pathologic / pathology*
  • PAX2 Transcription Factor / genetics
  • PAX2 Transcription Factor / metabolism*
  • Phenotype
  • Proteoglycans
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA, Antisense
  • Sarcoma, Kaposi / pathology

Substances

  • Chemokine CCL2
  • Drug Combinations
  • Laminin
  • PAX2 Transcription Factor
  • Proteoglycans
  • RNA, Antisense
  • matrigel
  • Intercellular Adhesion Molecule-1
  • Collagen
  • Proto-Oncogene Proteins c-akt