Ocaña-Morgner Carlos, Sales Susanne, Rothe Manuela, Shevchenko Andrej, Jessberger Rolf
Institute of Physiological Chemistry, Faculty of Medicine Carl Gustav Carus, Dresden University of Technology, Dresden 01307, Germany; and
Max Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.
J Immunol. 2017 Jun 1;198(11):4360-4372. doi: 10.4049/jimmunol.1601928. Epub 2017 May 3.
Lipids affect the membrane properties determining essential biological processes. Earlier studies have suggested a role of switch-activated protein 70 (SWAP-70) in lipid raft formation of dendritic cells. We used lipidomics combined with genetic and biochemical assays to analyze the role of SWAP-70 in lipid dynamics. TLR activation using LPS as a ligand represented a pathogenic immunogenic stimulus, physical disruption of cell-cell contacts a tolerogenic stimulus. Physical disruption, but not LPS, caused an increase of phosphatidylcholine ether and cholesteryl esters in CD11c immune cells. An increase of ceramide (Cer) was a hallmark for LPS activation. SWAP-70 was required for regulating the increase and localization of Cers in the cell membrane. SWAP-70 controls Cer accumulation through the regulation of pH-dependent acid-sphingomyelinase activity and of RhoA-dependent transport of endosomal contents to the plasma membrane. Poor accumulation of Cers in cells caused decreased apoptosis. This shows that two different pathways of activation, immunogenic and tolerogenic, induce different changes in the lipid composition of cultured CD11c cells, and highlights the important role of SWAP-70 in Cer dynamics in dendritic cells.
脂质会影响决定基本生物学过程的膜特性。早期研究表明,开关激活蛋白70(SWAP - 70)在树突状细胞的脂筏形成中发挥作用。我们运用脂质组学结合基因和生化分析方法,来剖析SWAP - 70在脂质动态变化中的作用。以脂多糖(LPS)作为配体进行Toll样受体(TLR)激活代表一种致病性免疫原性刺激,细胞间接触的物理破坏则是一种耐受性刺激。物理破坏而非LPS导致CD11c免疫细胞中磷脂酰胆碱醚和胆固醇酯增加。神经酰胺(Cer)增加是LPS激活的一个标志。SWAP - 70是调节细胞膜中Cers增加及定位所必需的。SWAP - 70通过调节pH依赖性酸性鞘磷脂酶活性以及RhoA依赖性内体内容物向质膜的转运来控制Cer积累。细胞中Cers积累不足导致细胞凋亡减少。这表明免疫原性和耐受性这两种不同的激活途径会诱导培养的CD11c细胞脂质组成发生不同变化,并突出了SWAP - 70在树突状细胞Cer动态变化中的重要作用。