MEMBRANES AND PHOSPHOLIPIDS IN RENAL HYPERPLASIA
MEMBRANES AND PHOSPHOLIPIDS IN RENAL HYPERPLASIA
批准号:
3236010
负责人:
FREDERICK Gary TOBACK
金额:
$23.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-04-01 至 1992-11-30
关键词:
Cercopithecidae biological signal transduction deficient growth media dietary potassium enzyme linked immunosorbent assay enzyme mechanism gene expression glyceraldehyde 3 phosphate dehydrogenase high performance liquid chromatography immunocytochemistry in situ hybridization kidney cell kidney hyperplasia kidney metabolism laboratory rat lipid metabolism membrane lipids membrane reconstitution /synthesis molecular cloning nucleic acid probes nutrition related tag pathogenic diet phospholipids potassium deficiency protein sequence protein structure function radiotracer renal cortex renal medulla tissue /cell culture transforming growth factors western blottings
中文摘要
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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.
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资助金额:$10.78万
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依托单位:
海外基金