Figure 1: Release of exosomes by tumour cells depends on aerobic glycolysis. | Nature Communications

Figure 1: Release of exosomes by tumour cells depends on aerobic glycolysis.

From: Pyruvate kinase type M2 promotes tumour cell exosome release via phosphorylating synaptosome-associated protein 23

Figure 1

(ac) Isolated exosomes from A549 cells assessed by transmission electron microscopy (a), WB (b) and NTA (c). The lower right image in a represents the immune-gold labelling of CD63 in an exosome. (d) Tumour cells release more exosomes than non-tumour cells. (e) Positive correlation between exosome secretion and aerobic glycolysis. (f) Linear regression between glucose uptake (r12=0.83) and lactate level (r 22=0.81). (g) Release of exosomes is dependent on cellular aerobic glycolysis. Cells were treated with shikonin (1 μM) or tumour necrosis factor α (5 ng ml−1) to inhibit or promote aerobic glycolysis. Exosome concentration was measured 24 h post-treatment. (h) Effect of EGF and OA on cell aerobic glycolysis. Note that EGF (10 ng ml−1), an enhancer of exosome release, increases aerobic glycolysis, while OA (10 μg ml−1), an inhibitor of exosome release, decreases aerobic glycolysis. (i) EGF and OA regulate A549 cell exosome release via altering cellular aerobic glycolysis. Data are presented as the mean±s.e.m. and represent at least three independent experiments with three replicates per data point. NS, no significance. *P<0.05, **P<0.01, **P<0.001 as determined by the one-way ANOVA test.

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