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Unsaturated fatty acids prevent activation of NLRP3 inflammasome in human monocytes/macrophages

机译:不饱和脂肪酸可阻止人单核细胞/巨噬细胞中NLRP3炎性小体的活化

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摘要

The NLRP3 inflammasome is involved in many obesity-associated diseases, such as type 2 diabetes, atherosclerosis, and gouty arthritis, through its ability to induce interleukin (IL)-1β release. The molecular link between obesity and inflammasome activation is still unclear, but free fatty acids have been proposed as one triggering event. Here we reported opposite effects of saturated fatty acids (SFAs) compared with unsaturated fatty acids (UFAs) on NLRP3 inflammasome in human monocytes/macrophages. Palmitate and stearate, both SFAs, triggered IL-1β secretion in a caspase-1/ASC/NLRP3-dependent pathway. Unlike SFAs, the UFAs oleate and linoleate did not lead to IL-1β secretion. In addition, they totally prevented the IL-1β release induced by SFAs and, with less efficiency, by a broad range of NLRP3 inducers, including nigericin, alum, and monosodium urate. UFAs did not affect the transcriptional effect of SFAs, suggesting a specific effect on the NLRP3 activation. These results provide a new anti-inflammatory mechanism of UFAs by preventing the activation of the NLRP3 inflammasome and, therefore, IL-1β processing. By this way, UFAs might play a protective role in NLRP3-associated diseases.
机译:NLRP3炎性小体通过其诱导白介素(IL)-1β释放的能力而参与许多与肥胖相关的疾病,例如2型糖尿病,动脉粥样硬化和痛风性关节炎。肥胖与炎症小体活化之间的分子联系仍不清楚,但已提出游离脂肪酸是一种触发事件。在这里,我们报道了饱和脂肪酸(SFA)与不饱和脂肪酸(UFA)对人单核细胞/巨噬细胞中NLRP3炎症小体的相反作用。棕榈酸酯和硬脂酸酯这两种SFA均以caspase-1 / ASC / NLRP3依赖性途径触发IL-1β分泌。与SFA不同,UFA的油酸酯和亚油酸酯不会导致IL-1β分泌。此外,它们完全阻止了由SFA诱导的IL-1β释放,并以较低的效率阻止了广泛的NLRP3诱导剂(包括黑霉素,明矾和尿酸一钠)的释放。 UFA不影响SFA的转录作用,表明对NLRP3激活具有特定作用。这些结果通过阻止NLRP3炎性小体的激活以及IL-1β的加工,提供了UFA的新抗炎机制。通过这种方式,UFA可能在与NLRP3相关的疾病中起保护作用。

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