Abstract | UNLABELLED: OBJECTIVE: Therefore, the capacity of PTX3 to alter the inflammatory milieu following in vitro stimulation of PBMCs with the pro-inflammatory lipid, palmitate, was examined. METHODS: PBMCs from 17 healthy male donors were isolated and cultured under four separate conditions; 200μmol/L palmitate, a physiologically relevant concentration of PTX3, in combination (pal+PTX3), and an unstimulated time-course control. RESULTS:
Palmitate-induced production of the counter-regulatory protein PTX3 was positively associated with the production of the anti-inflammatory cytokine interleukin 10 (IL-10) following in vitro stimulation of human PBMCs. Furthermore, stimulation of PBMCs in vitro with 500pg/mL PTX3 elicited a significantly greater increase in IL-10 production compared to the palmitate stimulated conditions. However, PTX3 stimulation did not result in the production of the pro-inflammatory cytokines IL-1β, IL-6, and tumor necrosis factor alpha, and when combined with palmitate, did not alter the pro-inflammatory milieu from PBMCs in this study. CONCLUSION: These findings provide evidence supporting the role of PTX3 as a mediator of the anti-inflammatory response in physiologically relevant conditions, and suggests that PTX3 counter regulates the development of atherosclerosis by enhancing the production of IL-10.
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Authors | Aaron L Slusher, Amanda B Mischo, Edmund O Acevedo |
Journal | Cytokine
(Cytokine)
Vol. 86
Pg. 36-40
(10 2016)
ISSN: 1096-0023 [Electronic] England |
PMID | 27450429
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2016 Elsevier Ltd. All rights reserved. |
Chemical References |
- Cytokines
- IL10 protein, human
- Lipopolysaccharides
- Serum Amyloid P-Component
- Tumor Necrosis Factor-alpha
- Interleukin-10
- PTX3 protein
- Palmitic Acid
- C-Reactive Protein
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Topics |
- Adult
- Atherosclerosis
(immunology)
- C-Reactive Protein
(immunology, metabolism)
- Cells, Cultured
- Cytokines
(metabolism)
- Humans
- Inflammation
- Interleukin-10
(immunology, metabolism)
- Leukocytes, Mononuclear
(immunology, metabolism)
- Lipopolysaccharides
(immunology)
- Male
- Palmitic Acid
(pharmacology)
- Serum Amyloid P-Component
(immunology, metabolism)
- Tumor Necrosis Factor-alpha
(metabolism)
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