| Tekijä(t): | Solakivi, Tiina; Kunnas, Tarja; Kärkkäinen, Satu; Jaakkola, Olli; Nikkari, Seppo T |
| Nimeke: | Arachidonic acid increases matrix metalloproteinase 9 secretion and expression in human monocytic MonoMac 6 cells |
| Vuosi: | 2009 |
| Lehden nimi: | Lipids in Health and Disease |
| Vol ja numero: |
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| Sivunumerot: | 1-8 |
| ISSN: | 1476-511X |
| Tieteenala: | Biolääketieteet |
| Julkaisun tyyppi: | Artikkeli aikakauslehdessä |
| Kieli: | en |
| DOI: | http://dx.doi.org/10.1186/1476-511X-8-11 |
| URN: | urn:nbn:uta-3-554 |
| Tiivistelmä: | Background
Dietary fatty acids may modulate inflammation in macrophages of the atherosclerotic plaque, affecting its stability. The n-6 polyunsaturated fatty acid (PUFA) arachidonic acid (AA) generally promotes inflammation, while the PUFAs of the n-3 series eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA) and docosahexaenoic acid (DHA) are considered anti-inflammatory. We determined how these PUFAs influence MMP-9 expression and secretion by the human monocytic cell line (MonoMac 6) at baseline and after 24-hour exposure. MMP-9 protein was measured by zymography and relative levels of MMP-9 mRNA were determined using quantitative real time PCR. Results Supplementation with AA (but not the n-3 fatty acids) increased, in a dose-dependent manner, expression of MMP-9 protein. This stimulation was regulated at the mRNA level. MMP-9 secretion started after 1 h of incubation and could not be prevented by simultaneous presence of n-3 series fatty acids. Finally, the secretion could be attenuated by LY 294002, a specific phosphatidylinositol-3-kinase (PI3K) inhibitor and by SH-5, a selective Akt inhibitor, suggesting that activation of PI3K by AA leads to augmented and sustained MMP-9 production. Conclusion This study shows that of the PUFA studied, AA alone influences the expression of MMP-9, which might have implications in MMP-9 induced plaque rupture. |
| Lisätiedot: | BioMed Central Open access |