Proinflammatory changes in human umbilical cord vein endothelial cells can be induced neither by native nor by modified CRP
| Autor: | Imre Gombos, Alma J Nauta, George Füst, Zoltán Prohászka, Eszter Herczenik, Anja Roos, Mohamed R. Daha, Szabolcs Rugonfalvi-Kiss, László Cervenak, Melinda Oroszlán, István Karádi, László Romics |
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| Rok vydání: | 2006 |
| Předmět: |
Umbilical Veins
medicine.medical_specialty Endothelium Protein Conformation Immunology Inflammation Biology Umbilical vein Proinflammatory cytokine Structure-Activity Relationship Internal medicine E-selectin medicine Humans Protein Isoforms Urea Immunology and Allergy Interleukin 8 Cell adhesion Cells Cultured Dose-Response Relationship Drug Monocyte Endothelial Cells General Medicine Atherosclerosis Recombinant Proteins C-Reactive Protein medicine.anatomical_structure Endocrinology Gene Expression Regulation biology.protein medicine.symptom |
| Zdroj: | International Immunology. 18:871-878 |
| ISSN: | 1460-2377 0953-8178 |
| DOI: | 10.1093/intimm/dxl023 |
| Popis: | The role of C-reactive protein (CRP) in atherosclerosis is controversial. It is not clear, either, if the presumed endothelium-activating effect of CRP resides in native CRP (nCRP) or in a conformational isoform of CRP known as modified CRP (mCRP). In the present study we evaluated and compared the effect of nCRP, recombinant modified CRP (rmCRP) and urea-modified CRP (umCRP) on human umbilical vein endothelial cells (HUVECs). CRP preparations were carefully analyzed by biochemical, immunological and cell biological methods in order to avoid endotoxin or sodium azide contamination as well as inappropriate conformational changes, which together had possibly been the main reason for the previously published controversial results. Neither nCRP nor mCRP showed significant cytotoxicity up to 100 microg ml(-1) at 24 h but high concentrations of CRPs induced cell death at 48 h. rmCRP but not nCRP nor umCRP showed membrane binding to HUVEC by confocal microscopy. However, none of the CRP forms induced intercellular cell adhesion molecule-1, vascular cell adhesion molecule-1, E-selectin expression or IL-8 production. Monocyte chemotactic protein-1 production was weakly inhibited by high concentration of both nCRP and rmCRP, analyzed by sandwich ELISA. Neither nCRP nor mCRP could induce pro-inflammatory changes in the phenotype of HUVECs. Therefore, our present findings do not support the notion that different isoforms of CRP alone have significant effects on inflammation of the vessel wall via an interaction with endothelial cells (ECs), although one cannot exclude the possibility that there may be significant differences among various types of ECs in the response to CRP. |
| Databáze: | OpenAIRE |
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