Vitamin B6 prevents excessive inflammation by reducing accumulation of sphingosine-1-phosphate in a sphingosine-1-phosphate lyase-dependent manner

被引:33
作者
Du, Xialin [1 ]
Yang, Yalong [1 ]
Zhan, Xiaoxia [2 ]
Huang, Yulan [1 ]
Fu, Yuling [1 ]
Zhang, Zelin [1 ]
Liu, Honglin [1 ]
Zhang, Lijie [1 ]
Li, Yanfen [1 ]
Wen, Qian [1 ]
Zhou, Xinying [1 ]
Zuo, Daming [1 ]
Zhou, Chaoying [1 ]
Li, Laisheng [2 ]
Hu, Shengfeng [1 ]
Ma, Li [1 ]
机构
[1] Southern Med Univ, Sch Lab Med & Biotechnol, Inst Mol Immunol, Guangzhou 510515, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Lab Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
anti-inflammatory; inflammatory disease; sphingosine-1-phosphate; sphingosine-1-phosphate lyase; Vitamin B6; METABOLISM; MACROPHAGES; ACTIVATION; DISEASE; MICE;
D O I
10.1111/jcmm.15917
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Vitamin B6 is necessary to maintain normal metabolism and immune response, especially the anti-inflammatory immune response. However, the exact mechanism by which vitamin B6 plays the anti-inflammatory role is still unclear. Here, we report a novel mechanism of preventing excessive inflammation by vitamin B6 via reduction in the accumulation of sphingosine-1-phosphate (S1P) in a S1P lyase (SPL)-dependent manner in macrophages. Vitamin B6 supplementation decreased the expression of pro-inflammatory cytokines by suppressing nuclear factor-kappa B and mitogen-activated protein kinases signalling pathways. Furthermore, vitamin B6-reduced accumulation of S1P by promoting SPL activity. The anti-inflammatory effects of vitamin B6 were inhibited by S1P supplementation or SPL deficiency. Importantly, vitamin B6 supplementation protected mice from lethal endotoxic shock and attenuated experimental autoimmune encephalomyelitis progression. Collectively, these findings revealed a novel anti-inflammatory mechanism of vitamin B6 and provided guidance on its clinical use.
引用
收藏
页码:13129 / 13138
页数:10
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