GLYCOSPHINGOLIPIDS OF HUMAN ENDOTHELIAL CELLS
GLYCOSPHINGOLIPIDS OF HUMAN ENDOTHELIAL CELLS
批准号:
3355166
负责人:
Baiba Kurins Gillard
金额:
$9.29万
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:
1987-08-01 至 1990-07-31
关键词:
atherosclerosis autoantibody binding proteins blood group antigens blood vessel disorder cell adhesion chemical binding coagulation factor VIII cytolysis fibronectins flow cytometry galactose oxidase gangliosides gas chromatography glycolipids glycosphingolipids high performance liquid chromatography human pregnant subject human tissue interferons interleukin 1 laminin leukocytes liposomes mass spectrometry membrane lipids methylation monoclonal antibody neutrophil nuclear magnetic resonance spectroscopy radioimmunoassay radiotracer receptor serology /serodiagnosis surface antigens thrombospondins tissue /cell culture umbilical cord vascular endothelium
中文摘要
内皮细胞的许多特殊特性是一种特殊的特性
英文摘要
Many of the specialized properties of endothelial cells are a
function of specific receptors and enzymes that are present on
their surface. Activation of endothelial cells by a variety of
stimuli causes striking changes in their expression of cell surface
molecules and in their functional properties. Glycosphingolipids
(GSLs) are cell surface molecules that are receptors and
immunogens. A number of blood group and tumor-associated
antigens are glycolipids, and autoantibodies to several glycolipids
have been identified recently. Although endothelial cells have
been the subject of intensive biochemical investigation, prior to
our work no information was available about the GSLs of these
cells. We have recently identified the major neutral GSLs and
gangliosides of human umbilical vein endothelial cells. The long
term objectives of our work are to determine whether an
immunological attack on endothelial cell GSLs plays a role in the
pathogenesis of vascular damage, and whether these GSLs are cell
surface receptors for regulatory molecules or cells. The specific
aims of this proposal are to identify changes in the composition
and cell surface expression of GSLs of lymphokine-activated
endothelial cells; to determine if cell surface GSLs mediate
binding of cells or adhesion proteins to activated endothelial cells;
and to analyze human sera for the presence of autoantibodies
against endothelial cell GSL antigens. These studies will provide
new information about an important class of endothelial cell
surface molecules, and will evaluate the role of GSLs as receptors
for immune cells and autoantibodies as a cause of vascular
damage and atherosclerosis.
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GLYCOSPHINGOLIPIDS OF HUMAN ENDOTHELIAL CELLS
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批准号:3355165
-
项目类别:
-
资助金额:$9.08万
-
财政年份:1987
-
负责人:Baiba Kurins Gillard
-
依托单位:
GLYCOSPHINGOLIPIDS OF HUMAN ENDOTHELIAL CELLS
-
批准号:3355163
-
项目类别:
-
资助金额:$10.79万
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财政年份:1987
-
负责人:Baiba Kurins Gillard
-
依托单位:
海外基金