Highly upregulated expression of CD36 and MSR1 in circulating monocytes of patients with acute coronary syndromes
Protein Journal, ISSN: 1875-8355, Vol: 31, Issue: 6, Page: 511-518
2012
- 34Citations
- 33Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations34
- Citation Indexes34
- 34
- CrossRef32
- Captures33
- Readers33
- 33
Article Description
Acute Coronary Syndromes (ACS) are a group of disorders caused by the significant reduction of circulation in coronary arteries. The most common reason of the dysfunction is a blood clot formed in place of plaque rupture. The role of scavenger receptors in development and progression of atherosclerosis has been confirmed in many animal experiments, however the knowledge about contribution of the receptors in the development of ACS symptoms in humans still remains insufficient. The aim of this work was to define the expression of two scavenger receptors: CD36 and MSR1 in monocytes of patients with ACS after the onset of symptoms and after the 6 months of treatment. The analysis of CD36 and MSR1 expression was carried out with the use of real-time PCR and flow cytometry. Analyses of lipid and glucose concentration in blood and the level of inflammatory markers in plasma were performed additionally for all ACS patients. All data obtained during the research were analyzed using statistical tests, such as Mann Whitney test, Wilcoxon test, or correlation. In all patients with symptoms of ACS the amount of CD36 and MSR1 mRNA in circulating monocytes, as well as the density of both receptors on the cells surface was significantly higher. Re-analysis of subjects after 6 months of treatment, showed a significant decrease in the CD36 and MSR1 expression in all patients who received atorvastatin. The results of presented studies demonstrate that both investigated receptors are involved in the development and/or progression of ACS. © 2012 Springer Science+Business Media, LLC.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84864718435&origin=inward; http://dx.doi.org/10.1007/s10930-012-9431-8; http://www.ncbi.nlm.nih.gov/pubmed/22763563; https://link.springer.com/10.1007/s10930-012-9431-8; https://dx.doi.org/10.1007/s10930-012-9431-8; https://link.springer.com/article/10.1007/s10930-012-9431-8; http://www.springerlink.com/index/10.1007/s10930-012-9431-8; http://www.springerlink.com/index/pdf/10.1007/s10930-012-9431-8
Springer Science and Business Media LLC
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