Matches in SemOpenAlex for { <https://semopenalex.org/work/W1992253100> ?p ?o ?g. }
- W1992253100 endingPage "e473" @default.
- W1992253100 startingPage "e473" @default.
- W1992253100 abstract "Human cytomegalovirus (hCMV) is involved in the pathogenesis of atherosclerosis. We have previously shown in patients with atherosclerosis that antibodies directed against the hCMV-derived proteins US28 and UL122 are able to induce endothelial cell damage and apoptosis of non-stressed endothelial cells through cross-rection with normally expressed surface molecules. Our aim was to dissect the molecular basis of such interaction and to investigate mechanisms linking innate immunity to atherosclerosis.We analysed the gene expression profiles in endothelial cells stimulated with antibodies affinity-purified against either the UL122 or the US28 peptides using the microarray technology. Microarray results were validated by quantitative PCR and by detection of proteins in the medium. Supernatant of endothelial cells incubated with antibodies was analysed also for the presence of Heat Shock Protein (HSP)60 and was used to assess stimulation of Toll-Like Receptor-4 (TLR4). Antibodies against UL122 and US28 induced the expression of genes encoding for adhesion molecules, chemokines, growth factors and molecules involved in the apoptotis process together with other genes known to be involved in the initiation and progression of the atherosclerotic process. HSP60 was released in the medium of cells incubated with anti-US28 antibodies and was able to engage TLR4.Antibodies directed against hCMV modulate the expression of genes coding for molecules involved in activation and apoptosis of endothelial cells, processes known to play a pivotal role in the pathogenesis of atherosclerosis. Moreover, endothelial cells exposed to such antibodies express HSP60 on the cell surface and release HSP60 in the medium able to activate TLR4. These data confirm that antibodies directed against hCMV-derived proteins US28 and UL122 purified from patients with coronary artery disease induce endothelial cell damage and support the hypothesis that hCMV infection may play a crucial role in mediating the atherosclerotic process." @default.
- W1992253100 created "2016-06-24" @default.
- W1992253100 creator A5000403129 @default.
- W1992253100 creator A5011154871 @default.
- W1992253100 creator A5026746758 @default.
- W1992253100 creator A5035205676 @default.
- W1992253100 creator A5056123741 @default.
- W1992253100 creator A5059468462 @default.
- W1992253100 creator A5060497601 @default.
- W1992253100 creator A5065548367 @default.
- W1992253100 creator A5065645344 @default.
- W1992253100 creator A5077922476 @default.
- W1992253100 date "2007-05-30" @default.
- W1992253100 modified "2023-10-17" @default.
- W1992253100 title "Endothelial Cells' Activation and Apoptosis Induced by a Subset of Antibodies against Human Cytomegalovirus: Relevance to the Pathogenesis of Atherosclerosis" @default.
- W1992253100 cites W1591714343 @default.
- W1992253100 cites W1970207578 @default.
- W1992253100 cites W1992207607 @default.
- W1992253100 cites W1995671732 @default.
- W1992253100 cites W2020789949 @default.
- W1992253100 cites W2025228141 @default.
- W1992253100 cites W2025869159 @default.
- W1992253100 cites W2032766057 @default.
- W1992253100 cites W2032791044 @default.
- W1992253100 cites W2054284944 @default.
- W1992253100 cites W2065095370 @default.
- W1992253100 cites W2071613661 @default.
- W1992253100 cites W2075972974 @default.
- W1992253100 cites W2105847016 @default.
- W1992253100 cites W2107480668 @default.
- W1992253100 cites W2112260972 @default.
- W1992253100 cites W2113902557 @default.
- W1992253100 cites W2120652037 @default.
- W1992253100 cites W2120653802 @default.
- W1992253100 cites W2121311096 @default.
- W1992253100 cites W2121934956 @default.
- W1992253100 cites W2124006262 @default.
- W1992253100 cites W2130668675 @default.
- W1992253100 cites W2131412402 @default.
- W1992253100 cites W2131464744 @default.
- W1992253100 cites W2136347732 @default.
- W1992253100 cites W2151124162 @default.
- W1992253100 cites W2158256445 @default.
- W1992253100 cites W2163584115 @default.
- W1992253100 cites W2164162150 @default.
- W1992253100 cites W2165884492 @default.
- W1992253100 cites W2324841714 @default.
- W1992253100 cites W2418490055 @default.
- W1992253100 cites W303348942 @default.
- W1992253100 cites W112051748 @default.
- W1992253100 cites W1778838840 @default.
- W1992253100 doi "https://doi.org/10.1371/journal.pone.0000473" @default.
- W1992253100 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1868596" @default.
- W1992253100 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17534423" @default.
- W1992253100 hasPublicationYear "2007" @default.
- W1992253100 type Work @default.
- W1992253100 sameAs 1992253100 @default.
- W1992253100 citedByCount "35" @default.
- W1992253100 countsByYear W19922531002013 @default.
- W1992253100 countsByYear W19922531002014 @default.
- W1992253100 countsByYear W19922531002015 @default.
- W1992253100 countsByYear W19922531002016 @default.
- W1992253100 countsByYear W19922531002017 @default.
- W1992253100 countsByYear W19922531002018 @default.
- W1992253100 countsByYear W19922531002019 @default.
- W1992253100 countsByYear W19922531002020 @default.
- W1992253100 countsByYear W19922531002021 @default.
- W1992253100 countsByYear W19922531002023 @default.
- W1992253100 crossrefType "journal-article" @default.
- W1992253100 hasAuthorship W1992253100A5000403129 @default.
- W1992253100 hasAuthorship W1992253100A5011154871 @default.
- W1992253100 hasAuthorship W1992253100A5026746758 @default.
- W1992253100 hasAuthorship W1992253100A5035205676 @default.
- W1992253100 hasAuthorship W1992253100A5056123741 @default.
- W1992253100 hasAuthorship W1992253100A5059468462 @default.
- W1992253100 hasAuthorship W1992253100A5060497601 @default.
- W1992253100 hasAuthorship W1992253100A5065548367 @default.
- W1992253100 hasAuthorship W1992253100A5065645344 @default.
- W1992253100 hasAuthorship W1992253100A5077922476 @default.
- W1992253100 hasBestOaLocation W19922531001 @default.
- W1992253100 hasConcept C104317684 @default.
- W1992253100 hasConcept C123012128 @default.
- W1992253100 hasConcept C13373296 @default.
- W1992253100 hasConcept C136449434 @default.
- W1992253100 hasConcept C146621620 @default.
- W1992253100 hasConcept C153911025 @default.
- W1992253100 hasConcept C159654299 @default.
- W1992253100 hasConcept C16224149 @default.
- W1992253100 hasConcept C202751555 @default.
- W1992253100 hasConcept C203014093 @default.
- W1992253100 hasConcept C205260736 @default.
- W1992253100 hasConcept C2780942790 @default.
- W1992253100 hasConcept C54355233 @default.
- W1992253100 hasConcept C68991219 @default.
- W1992253100 hasConcept C86803240 @default.
- W1992253100 hasConcept C8891405 @default.
- W1992253100 hasConcept C95444343 @default.
- W1992253100 hasConceptScore W1992253100C104317684 @default.