课题基金 / 基金详情

项目摘要

项目成果

FREDERICK Gary TOBACK的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
THe long-term objective of this project is to elucidate molecular mechanisms by which a reduction in extracellular potassium (K) concentration is transduced into a mitogenic signal by renal epithelial cells. Kidney growth is induced in rats fed a diet deficient in K, and can be reversed by returning K to the chow. We have shown that cell proliferation, organelle biogenesis, and phospholipid biosynthesis for new cellular membranes in this experimental model can be turned on and off by this simple dietary manipulation. The kidneys of rats fed a K-medium for 1 hour exhibit enhanced glycolysis, activation of the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (G3PD), and accelerated growth. The rapid activation of G3PD is mediated by a cytosolic protein was purified from the cytosol of BSC-1 cells exposed to the low-K mitogenic signal, and subjected to enzymatic cleavage. Amino acid microsequencing of five of the peptide fragments revealed that the modifier is a novel protein. Recent studies utilizing a monospecific antibody revealed that an increased amount of immunoreactive protein and modifier function are present in rat renal papilla and inner stripe of red medulla during the onset of K depletion nephropathy. A new protocol to rapidly purify the modifier has been developed, using an immunoaffinity column, that will facilitate studies aimed at defining the structure and function of this protein. The specific aims of this revised application are to: 1. use new strategies to obtain a cDNA clone from monkey kidney epithelial cells or rat kidney tissue which encodes the G3PD modifier, and use it to predict the amino acid sequence of the protein; 2. use the cDNA clone to study the regulation of gene expression in normal and proliferation kidney tissue, and 3. use the monospecific antibody to elucidate the contribution of the modifier protein to control of cell growth. Achieving these aims could elucidate the role of the G3PD modifier protein and K in physiological and pathological states.
期刊论文(30)
专著(0)
科研奖励(0)
会议论文
Aberrant responses to growth-regulatory signals by variant kidney epithelial cells.
变异肾上皮细胞对生长调节信号的异常反应。
DOI: 10.1152/ajprenal.1988.254.5.f747
发表时间: 1988
期刊: The American journal of physiology
影响因子: --
作者: [Walsh-Reitz,MM, Feldman,RI, Toback,FG]
通讯作者: Toback,FG
Purine nucleotides stimulate DNA synthesis in kidney epithelial cells in culture.
嘌呤核苷酸刺激培养的肾上皮细胞中的 DNA 合成。
DOI: 10.1152/ajprenal.1985.249.6.f967
发表时间: 1985
期刊: The American journal of physiology
影响因子: --
作者: [Kartha,S, Toback,FG]
通讯作者: Toback,FG
Growth of kidney epithelial cells in culture: evidence for autocrine control.
培养物中肾上皮细胞的生长:自分泌控制的证据。
DOI: 10.1152/ajpcell.1984.246.3.c351
发表时间: 1984
期刊: The American journal of physiology
影响因子: --
作者: [Mordan,LJ, Toback,FG]
通讯作者: Toback,FG
Phosphatidylcholine metabolism during renal growth and regeneration.
肾脏生长和再生过程中的磷脂酰胆碱代谢。
DOI: 10.1152/ajprenal.1984.246.3.f249
发表时间: 1984
期刊: The American journal of physiology
影响因子: --
作者: [Toback,FG]
通讯作者: Toback,FG
27
    A Novel Agent with Dual Functions to Treat Head and Neck Cancer
    • 批准号:
      8638361
    • 项目类别:
    • 资助金额:
      $20.62万
    • 财政年份:
      2014
    • 负责人:
      FREDERICK Gary TOBACK
    • 依托单位:
    A Novel Agent with Dual Functions to Treat Head and Neck Cancer
    • 批准号:
      8777091
    • 项目类别:
    • 资助金额:
      $17.18万
    • 财政年份:
      2014
    • 负责人:
      FREDERICK Gary TOBACK
    • 依托单位:
    Targeting Tight Junctions To Treat Mucositis
    • 批准号:
      7817005
    • 项目类别:
    • 资助金额:
      $23.4万
    • 财政年份:
      2009
    • 负责人:
      FREDERICK Gary TOBACK
    • 依托单位:
    Targeting Tight Junctions To Treat Mucositis
    • 批准号:
      7660772
    • 项目类别:
    • 资助金额:
      $19.5万
    • 财政年份:
      2009
    • 负责人:
      FREDERICK Gary TOBACK
    • 依托单位:
    海外基金