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Transcriptomic profiling identifies ferroptosis and NF-κB signaling involved in α-dimorphecolic acid regulation of
Xiao-Xi Zhu1, Pei-Juan Wang2, Shan Chao3
1Key Laboratory of Cell Engineering in Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Background:
Microglia-evoked neuroinflammation contributes to neurodegenerative diseases such as multiple sclerosis (MS). Metabolic reprogramming, including changes in polyunsaturated fatty acids (PUFAs), plays a critical role in MS pathophysiology. Previous studies identified reduced plasma α-dimorphecolic acid (α-DIPA), a linoleic acid derivative, in MS patients. This study investigated the anti-inflammatory effects of α-DIPA on microglia and the underlying pathways.
Methods:
Lipopolysaccharide (LPS)-induced BV-2 microglial inflammation was used as an in vitro model. α-DIPA effects were assessed via ELISA for nitric oxide (NO) release, flow cytometry was used to examine cell proliferation, activation and polarization, and transcriptomic analysis was applied to identify key signaling pathways regulated by α-DIPA.
Results:
ELISA results showed that exogenous α-DIPA treatment significantly inhibited LPS-induced NO release from BV-2 cells in a concentration-dependent manner. Moreover, flow cytometry analysis suggested that 40 µM α-DIPA treatment significantly repressed LPS-induced BV-2 cell proliferation, activation, as well as M1 and M2 type polarization. Furthermore, transcriptome analysis revealed that exogenous α-DIPA extensively and drastically decreased the transcriptional level of numerous genes that are involved in the regulation of inflammatory responses, for instance, proinflammatory genes such as Tnf and Ccl3 related to IL-17 and TNF-α signaling. In addition, we also observed that the expression of multiple genes in NF-κB signaling were also inhibited greatly by α-DIPA, such as Nfkb2 and Nfkbia. Notably, α-DIPA robustly suppressed LPS-induced mRNA expression of abundant genes participating in the ferroptosis pathway, including Acsl4, Slc7a11, Me1, and Hmox1. Interestingly, the expressions of multiple ferroptosis-related genes were regulated specifically by α-DIPA but not LPS, such as Acsl5, Acsl6, Alox5, Cars, Dpp3, Dpp10, Slc2a5, and Slc7a1.
Conclusion:
α-DIPA inhibits microglial inflammation likely through regulating the pathways of the ferroptosis and NF-κB signaling. These results provided preliminary evidence for α-DIPA as a potential therapeutic candidate for neurodegenerative diseases like MS.
Insights
Alpha-dimorphecolic acid (α-DIPA) reduces microglial inflammation by inhibiting nitric oxide release and cell activation. This polyunsaturated fatty acid derivative shows potential as a therapeutic for neurodegenerative diseases like multiple sclerosis.
Area of Science:
- Neuroscience
- Immunology
- Biochemistry
Background:
- Microglia-driven neuroinflammation is implicated in neurodegenerative diseases such as multiple sclerosis (MS).
- Metabolic alterations, particularly in polyunsaturated fatty acids (PUFAs), are crucial in MS.
- Reduced plasma levels of alpha-dimorphecolic acid (α-DIPA), a linoleic acid metabolite, are observed in MS patients.
Purpose of the Study:
- To investigate the anti-inflammatory effects of α-DIPA on microglia.
- To elucidate the molecular pathways modulated by α-DIPA in microglial inflammation.
Main Methods:
- Utilized lipopolysaccharide (LPS)-induced BV-2 microglial cells as an in vitro model.
- Assessed nitric oxide (NO) release using ELISA.
- Analyzed cell proliferation, activation, and polarization via flow cytometry.
- Employed transcriptomic analysis to identify signaling pathways regulated by α-DIPA.
Main Results:
- α-DIPA significantly inhibited LPS-induced NO release in a dose-dependent manner.
- α-DIPA suppressed LPS-induced microglial proliferation, activation, and M1/M2 polarization.
- Transcriptomic analysis revealed α-DIPA downregulated inflammatory genes (e.g., Tnf, Ccl3) and NF-κB signaling pathway components (e.g., Nfkb2, Nfkbia).
- α-DIPA notably suppressed genes involved in ferroptosis, including Acsl4 and Slc7a11, and modulated other ferroptosis-related genes.
Conclusions:
- α-DIPA exerts anti-inflammatory effects on microglia by modulating ferroptosis and NF-κB signaling pathways.
- These findings suggest α-DIPA as a potential therapeutic agent for neurodegenerative conditions like MS.
