Human immunodeficiency virus type 1 Tat protein modulates cell cycle and apoptosis in Epstein-Barr virus-immortalized B cells

Exp Cell Res. 2004 May 1;295(2):539-48. doi: 10.1016/j.yexcr.2004.01.018.

Abstract

Patients infected with human immunodeficiency virus type 1 (HIV-1) develop a spectrum of B cell lymphoproliferative disorders ranging from polyclonal B cell activation to B cell lymphomas. While a direct role of Epstein-Barr virus (EBV) is well recognized for most of these lesions, recent findings have suggested that transactivator HIV-1 Tat protein might be involved in the pathogenesis of B cell lymphomas. Tat-expressing EBV-positive B cells were generated by transduction with a retroviral Tat-encoding vector. B(Tat+) cells expressed lower levels of anti-apoptotic protein Bcl-2 than parental and control B(Tat-) cells, generated by transduction with an empty retroviral vector, and were more prone to apoptosis upon serum withdrawal, as assessed by analysis of annexin V-stained cells and cleavage of poly-ADP-ribose-polymerase by caspase 3. Nevertheless, in serum starvation, B(Tat-) cells mainly exhibited the Rb hypo-phosphorylated form, underwent cell cycle arrest, and grew in single cell suspension, while B(Tat+) cells displayed the Rb hyper-phoshorylated form, progressed throughout the cell cycle, and retained the ability to grow in small clumps. Finding that B(Tat+) cells maintained proliferative capacity upon serum withdrawal suggests that cells expressing Tat have growth advantages among the EBV-driven cell proliferations and may originate B cell clones with more oncogenic potential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Annexin A5 / metabolism
  • Apoptosis*
  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / virology*
  • Caspases / metabolism
  • Cell Cycle*
  • Cell Division
  • Cell Line
  • Cell Line, Transformed
  • Cell Transformation, Viral
  • Culture Media, Serum-Free
  • Gene Expression Regulation, Viral
  • Gene Products, tat / genetics
  • Gene Products, tat / metabolism*
  • HIV-1 / physiology*
  • Herpesvirus 4, Human / physiology*
  • Humans
  • Phosphorylation
  • Retinoblastoma / genetics
  • Retinoblastoma / metabolism
  • Retroviridae / genetics
  • Viral Proteins / analysis
  • Viral Proteins / metabolism
  • tat Gene Products, Human Immunodeficiency Virus

Substances

  • Annexin A5
  • Culture Media, Serum-Free
  • Gene Products, tat
  • Viral Proteins
  • tat Gene Products, Human Immunodeficiency Virus
  • Caspases