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LPS and palmitate synergistically stimulate sphingosine kinase 1 and increase sphingosine 1 phosphate in RAW264.7 macrophages

促炎细胞因子 鞘氨醇激酶 神经酰胺 脂质信号 鞘氨醇激酶1 1-磷酸鞘氨醇 下调和上调 鞘氨醇 生物 细胞因子 内分泌学 炎症 内科学 生物化学 受体 免疫学 细胞凋亡 医学 基因
作者
Junfei Jin,Zhongyang Lu,Yanchun Li,Ji Hyun Ru,Maria F. Lopes‐Virella,Yan Huang
出处
期刊:Journal of Leukocyte Biology [Oxford University Press]
卷期号:104 (4): 843-853 被引量:26
标识
DOI:10.1002/jlb.3a0517-188rrr
摘要

Abstract It has been well established that patients with diabetes or metabolic syndrome (MetS) have increased prevalence and severity of periodontitis, an oral infection initiated by bacteria and characterized by tissue inflammation and destruction. To understand the underlying mechanisms, we have shown that saturated fatty acid (SFA), which is increased in patients with type 2 diabetes or MetS, and LPS, an important pathogenic factor for periodontitis, synergistically stimulate expression of proinflammatory cytokines in macrophages by increasing ceramide production. However, the mechanisms by which increased ceramide enhances proinflammatory cytokine expression have not been well understood. Since sphingosine 1 phosphate (S1P) is a metabolite of ceramide and a bioactive lipid, we tested our hypothesis that stimulation of ceramide production by LPS and SFA facilitates S1P production, which contributes to proinflammatory cytokine expression. Results showed that LPS and palmitate, a major SFA, synergistically increased not only ceramide, but also S1P, and stimulated sphingosine kinase (SK) expression and membrane translocation in RAW264.7 macrophages. Results also showed that SK inhibition attenuated the stimulatory effect of LPS and palmitate on IL-6 secretion. Moreover, results showed that S1P enhanced the stimulatory effect of LPS and palmitate on IL-6 secretion. Finally, results showed that targeting S1P receptors using either S1P receptor antagonists or small interfering RNA attenuated IL-6 upregulation by LPS and palmitate. Taken together, this study demonstrated that LPS and palmitate synergistically stimulated S1P production and S1P in turn contributed to the upregulation of proinflammatory cytokine expression in macrophages by LPS and palmitate. LPS and palmitate synergistically increase S1P and, in turn, S1P contributes to upregulation of proinflammatory genes by LPS and palmitate.
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