NOVEL GROWTH FACTOR RELEASED BY KIDNEY EPITHELIAL CELLS
NOVEL GROWTH FACTOR RELEASED BY KIDNEY EPITHELIAL CELLS
批准号:
3239575
负责人:
FREDERICK Gary TOBACK
金额:
$14.94万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1987
资助国家:
美国
项目状态:
已结题
起止时间:
1987-09-30 至 1995-03-31
关键词:
autocrine complementary DNA deficient growth media enzyme linked immunosorbent assay epithelium gene expression growth factor growth factor receptors high performance liquid chromatography immunologic assay /test in situ hybridization ion transport kidney cell laboratory rat messenger RNA molecular cloning northern blottings nucleic acid probes protein sequence protein structure function sodium tissue /cell culture
中文摘要
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英文摘要
The goal of this project is to define the physiological significance of an
apparently novel protein that stimulates growth of kidney epithelial
cells.
We previously identified a protein that appears when nontransformed monkey
renal epithelial cells (BSC-1 line) are exposed for 3-5 minutes to a
reduced concentration of sodium in the culture medium; it is called the
low sodium growth factor (LSGF). This protein has an apparent molecular
weight about 6,500, stimulates growth of both monkey and canine kidney
epithelial cells in culture but not fibroblasts, resists denaturation by
dithiothreitol, appears to differ from known growth factors of similar
size with respect to biological activity and amino acid composition, and
resides in the extracellular matrix from which it is released when the
sodium concentration of the medium is reduced. The amino terminus of the
LSGF protein is blocked. A protocol to purify LSGF by reversed-phase (RP)
HPLC was developed during the 03 grant year.
This revised application describes a new biologically active isoform of
LSGF detected by RP HPLC that has a different amino acid composition than
the previously described protein. In addition, a rabbit antiserum against
LSGF has been prepared that recognizes both LSGF isoforms of ELISA, and
also neutralizes the growth-promoting activity of each. To define the
structure of LSGF and mechanisms by which it exerts its physiological
effects on renal cells in vitro and in vivo, new reagents are required
that will be used to achieve the following specific aims:
1. partially sequence the LSGF protein;
2. use oligonucleotide probes or immunoscreening to clone the gene that
encodes the protein, and study regulation of its expression during cell
growth;
3. develop LSGF immunoassays to study the physiology the protein;
4. determine if LSGF alters nutrient and ion transport in renal epithelial
cells.
Achieving these aims could define the role of this autocrine growth factor
in renal physiology and pathophysiology. Identifying mechanisms by which
the LSGF acts may be an important step towards our long-term goal of
formulating a therapeutic solution containing specific components such as
nutrients and growth factors that could speed regeneration of the kidney
after injury.
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海外基金