Effects of cytokines, growth factors, extracellular matrix proteins and recent evidence of viral proteins on pluripotent stem cell differentiation has led the applicant to hypothesize that viral Tat and/or Nef proteins may affect the overall proliferation and differentiation of the hematopoietic progenitor cells via alteration of production of the various cytokines in the stromal cells and/or induction of a direct inhibitory effect on the CD34+ cells. To test this hypothesis, the P.I. proposes to investigate the effects of Tat and/or Nef proteins, either directly or by the co-culture techniques utilizing the HeLa-tat and/or HeLa-nef stably transfected cell lines on the primary CD34+ cells, the stromal cells and the transformed progenitor cells, K562 and HL-60. Specifically, following aims will be investigated: (1) proliferation and differentiation of CD34+ cells, and K-562 and HL-60 cells in the presence and absence of stromal cells both untreated and pretreated with the viral proteins; (2) the effect of the viral proteins on signal transduction pathways; (3) the levels of cytokines released by the stromal cells and monitoring of the corresponding mRNA levels; (4) the expression of protooncogenes and of the cell surface receptors; (5) the modulation of the function of various transcription factors via direct protein-protein interactions; and (6) the mechanisms that may be responsible for the viral protein-induced modulation of apoptotic pathways in the progenitor cells. The applicant believes that the proposed experiments will provide an in-depth understanding of the mechanisms that may be involved in HIV-induced hematopoietic suppression.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL058409-02
Application #
2735379
Study Section
AIDS and Related Research Study Section 4 (ARRD)
Project Start
1997-08-01
Project End
2001-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Tulane University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Mondal, Debasis; Williams, Christopher A; Ali, Mussa et al. (2005) The HIV-1 Tat protein selectively enhances CXCR4 and inhibits CCR5 expression in megakaryocytic K562 cells. Exp Biol Med (Maywood) 230:631-44
Williams, Christopher A; Mondal, Debasis; Agrawal, Krishna C (2005) The HIV-1 Tat protein enhances megakaryocytic commitment of K562 cells by facilitating CREB transcription factor coactivation by CBP. Exp Biol Med (Maywood) 230:872-84
Abdel-Mageed, Asim B; Zhao, Fusheng; Rider, Barbara J et al. (2003) Erythropoietin-induced metallothionein gene expression: role in proliferation of K562 cells. Exp Biol Med (Maywood) 228:1033-9