"State Key Laboratory of Food Nutrition and Safety", Key Laboratory of Food Nutrition and Safety, Ministry of Education, College of Food Engineering and Biotechnology, Tianjin University of Science and Technology, No. 29, 13th Avenue, Tianjin Economy Technological Development Area, Tianjin, 300457, People Republic of China.
Food Funct. 2020 Mar 26;11(3):2603-2616. doi: 10.1039/c9fo02618e.
DHA can regulate various physiological functions of cells. Our group has clarified the immunomodulatory activity and molecular mechanism of DHA on RAW264.7 cells. However, the effect of DHA on the membrane fatty acid environment and the activation of signaling pathways on the cell membrane is still not clear.
In this study, we evaluated the fluidity, the potential and the fatty acid, phospholipid and protein composition of the RAW264.7 cell membrane by DHA treatment.
The fluidity of the RAW264.7 cell membrane was increased by DHA treatment. The results of membrane potential analysis suggested that DHA (2.4 μM) significantly reduced the surface potential of the cell membrane, which might influence the fluidity of cell membranes. In addition, the fatty acids and phospholipids were measured and the results indicated that DHA treatment (2.4 μM) altered the lipid environment and the composition of phospholipids on the RAW264.7 cell membrane. Then the LC-MS/MS-based label free quantitative proteomics approach was applied to identify a total of 86 differential proteins in the 2.4 μM DHA and control groups (>2.0-fold change or <0.5-fold change in protein expression); these proteins are most frequently related to the cell response to stimuli and the response to stress. These results suggested that DHA could alter the fluidity, the potential, the fatty acid and phospholipid composition of the RAW264.7 cell membrane, eventually affecting the proteins of the cell membrane, especially the changes in Siglec 1, iNOS, GPR120, Ras and MEK expressions (validated by western blot analysis), which are likely associated with the activation of the intracellular signaling pathway in RAW264.7 cells by DHA treatment.
DHA 可以调节细胞的各种生理功能。我们的研究小组已经阐明了 DHA 对 RAW264.7 细胞的免疫调节活性和分子机制。然而,DHA 对细胞膜脂肪酸环境以及细胞膜上信号通路的激活的影响尚不清楚。
在本研究中,我们通过 DHA 处理来评估 RAW264.7 细胞膜的流动性、潜能以及脂肪酸、磷脂和蛋白质组成。
DHA 处理增加了 RAW264.7 细胞膜的流动性。膜电位分析结果表明,DHA(2.4 μM)显著降低了细胞膜的表面电位,这可能影响细胞膜的流动性。此外,还测量了脂肪酸和磷脂,结果表明 DHA 处理(2.4 μM)改变了 RAW264.7 细胞膜上的脂质环境和磷脂组成。然后应用基于 LC-MS/MS 的无标记定量蛋白质组学方法来鉴定 2.4 μM DHA 和对照组中总共 86 个差异蛋白(蛋白表达变化超过 2.0 倍或小于 0.5 倍);这些蛋白最常与细胞对刺激的反应和对压力的反应有关。这些结果表明,DHA 可以改变 RAW264.7 细胞膜的流动性、潜能、脂肪酸和磷脂组成,最终影响细胞膜的蛋白质,特别是 Siglec 1、iNOS、GPR120、Ras 和 MEK 表达的变化(通过 Western blot 分析验证),这可能与 DHA 处理激活 RAW264.7 细胞内的信号通路有关。