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Fig. 5 | Journal of Neuroinflammation

Fig. 5

From: Parkinson’s disease-derived α-synuclein assemblies combined with chronic-type inflammatory cues promote a neurotoxic microglial phenotype

Fig. 5

Microglial metabolic reprogramming evoked by TPFPD is closely related to M1-type polarized cells. A Hierarchical clustering analysis and heatmap visualization of 248 differentially regulated metabolites (28 annotated and 220 unknown/nonannotated metabolites) in stimulated cells (LPS and TPFPD) compared to those in the NSC control group. The number of biological replicates is indicated in brackets. Clear changes in the metabolic profile between stimulated and nonstimulated cells are observed. B Hierarchical clustering analysis and heatmap visualization of the 28 annotated metabolites extracted from A. Despite these subtle differences, the TPFPD- and LPS-associated metabolic signatures are closely related. C Box plots showing the relative amount of α-ketoglutarate, succinate, fumarate, glutamate and glutathione disulfide (GSSG) in control (NSC) and in LPS- and TPFPD-treated microglial cells. Similar decreases in the α-ketoglutarate/succinate and fumarate/succinate ratios were found in LPS- and TPFPD-stimulated cells. Likewise, similar increases in glutamate and GSSG levels were observed under both stimulatory conditions. *p < 0.05 (Kruskal–Wallis and Wilcoxon test)

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