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MECHANISMS OF HEMATOLOGIC ABNORMALITIES IN AIDS

MECHANISMS OF HEMATOLOGIC ABNORMALITIES IN AIDS
艾滋病血液学异常的机制
批准号:
6183968
负责人:
Krishna C. Agrawal
金额:
$27.45万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-08-01 至 2002-12-31

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DESCRIPTION (Adapted from the Investigator's Abstract): 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.
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The HIV-1 Tat protein enhances megakaryocytic commitment of K562 cells by facilitating CREB transcription factor coactivation by CBP.
HIV-1 Tat 蛋白通过促进 CBP 共激活 CREB ​​转录因子来增强 K562 细胞的巨核细胞定型。
DOI: 10.1177/153537020523001113
发表时间: 2005
期刊: Experimental biology and medicine (Maywood, N.J.)
影响因子: --
作者: [Williams,ChristopherA, Mondal,Debasis, Agrawal,KrishnaC]
通讯作者: Agrawal,KrishnaC
The HIV-1 Tat protein selectively enhances CXCR4 and inhibits CCR5 expression in megakaryocytic K562 cells.
HIV-1 Tat 蛋白选择性增强巨核细胞 K562 细胞中 CXCR4 的表达并抑制 CCR5 的表达。
DOI: 10.1177/153537020523000905
发表时间: 2005
期刊: Experimental biology and medicine (Maywood, N.J.)
影响因子: --
作者: [Mondal,Debasis, Williams,ChristopherA, Ali,Mussa, Eilers,Mark, Agrawal,KrishnaC]
通讯作者: Agrawal,KrishnaC
Mechanisms of HAART-Induced Endothelial Dysfunction
  • 批准号:
    7086954
  • 项目类别:
  • 资助金额:
    $34.09万
  • 财政年份:
    2003
  • 负责人:
    Krishna C. Agrawal
  • 依托单位:
Mechanisms of HAART-Induced Endothelial Dysfunction
  • 批准号:
    7291423
  • 项目类别:
  • 资助金额:
    $36.37万
  • 财政年份:
    2003
  • 负责人:
    Krishna C. Agrawal
  • 依托单位:
Mechanisms of HAART-Induced Endothelial Dysfunction
  • 批准号:
    6765886
  • 项目类别:
  • 资助金额:
    $37.13万
  • 财政年份:
    2003
  • 负责人:
    Krishna C. Agrawal
  • 依托单位:
Mechanisms of HAART-Induced Endothelial Dysfunction
  • 批准号:
    6915196
  • 项目类别:
  • 资助金额:
    $37.13万
  • 财政年份:
    2003
  • 负责人:
    Krishna C. Agrawal
  • 依托单位:
海外基金