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Status |
Public on Apr 01, 2008 |
Title |
Imprints of atherosclerosis are present in circulating T cells of patients with Familial Hypercholesterolemia |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Atherosclerosis is the major cause of death in industrialized countries. This disease has initially been characterized as a lipid disorder, but current concepts argue for an inflammatory disease, which develops in the background of hypercholesterolemia and other risk factors. In response to initial events of atherosclerosis formation, such as LDL-deposition in the subendothelial space, monocytes and T cells interact with the vessel wall. However, little is known about the properties and the behavior of these cells in this context. Using familial hypercholesterolemia (FH) as a model we demonstrate substantial differences in the gene expression of freshly isolated human monocytes and T lymphocytes. In FH monocytes we found an increased uptake of oxidized LDL, elevated amounts of scavenger receptors and adhesion molecules, and differences in the regulation of intracellular lipoprotein metabolism compared to monocytes from healthy individuals. Furthermore, the monocyte subpopulation of CD14+/CD16+ cells is less frequent in FH but exhibits significantly higher levels of CD11c and CD29 which increases the likelihood for their transmigration through the endothelial layer. The presence of increased amounts of CD69 in T lymphocytes from FH patients suggests that these cells are more activated than control cells. Our results indicate that some important steps of atherosclerosis formation already take place in circulating blood cells which extends current atherosclerosis models to the plasma compartment. Keywords: atherosclerosis, T cells, Familial Hypercholesterolemia
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Overall design |
23 T cells samples: 3 homozygous FH, 7 heterozygous FH, 13 control participants
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Contributor(s) |
Mosig S, Rennert K, Buettner P, Soufi M, Krause S, Kzhyshkowska J, Goerdt S, Heller R, Schaefer J, Funke H, Kuehn B, Neunuebel K, Schreiner T |
Citation missing |
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Submission date |
Oct 20, 2006 |
Last update date |
Mar 25, 2019 |
Contact name |
Sandy Mosig |
E-mail(s) |
sandy.mosig@mti.uni-jena.de, sandy.mosig@googlemail.com
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Phone |
+49-3641-934813
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Fax |
+49-3641-933950
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Organization name |
University Hospital Jena
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Department |
Molecular Hemostaseology - Institute of Vascular Medicine
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Street address |
Bachstrasse 18
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City |
Jena |
ZIP/Postal code |
07743 |
Country |
Germany |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (23)
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Relations |
BioProject |
PRJNA97641 |
Supplementary file |
Size |
Download |
File type/resource |
GSE6088_RAW.tar |
103.2 Mb |
(http)(custom) |
TAR (of CEL) |
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