Quantitative Proteomics Reveals Docosahexaenoic Acid-Mediated Neuroprotective Effects in Lipopolysaccharide-Stimulated Microglial Cells.
Bo YangRunting LiPei N LiuXue GengBrian P MooneyChen ChenJianlin ChengKevin L FritscheDavid Q BeversdorfJames C LeeGrace Y SunCharles Michael GreenliefPublished in: Journal of proteome research (2020)
The high levels of docosahexaenoic acid (DHA) in cell membranes within the brain have led to a number of studies exploring its function. These studies have shown that DHA can reduce inflammatory responses in microglial cells. However, the method of action is poorly understood. Here, we report the effects of DHA on microglial cells stimulated with lipopolysaccharides (LPSs). Data were acquired using the parallel accumulation serial fragmentation method in a hybrid trapped ion mobility-quadrupole time-of-flight mass spectrometer. Over 2800 proteins are identified using label-free quantitative proteomics. Cells exposed to LPSs and/or DHA resulted in changes in cell morphology and expression of 49 proteins with differential abundance (greater than 1.5-fold change). The data provide details about pathways that are influenced in this system including the nuclear factor κ-light-chain-enhancer of the activated B cells (NF-κB) pathway. Western blots and enzyme-linked immunosorbent assay studies are used to help confirm the proteomic results. The MS data are available at ProteomeXchange.
Keyphrases
- induced apoptosis
- label free
- cell cycle arrest
- mass spectrometry
- nuclear factor
- fatty acid
- inflammatory response
- lps induced
- toll like receptor
- signaling pathway
- oxidative stress
- electronic health record
- lipopolysaccharide induced
- poor prognosis
- neuropathic pain
- ms ms
- multiple sclerosis
- big data
- endoplasmic reticulum stress
- pi k akt
- microbial community
- transcription factor
- cell therapy
- liquid chromatography
- long non coding rna
- mesenchymal stem cells
- cell proliferation
- white matter
- functional connectivity
- brain injury