Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 1 | Journal of Biomedical Science

Fig. 1

From: Blocking the SIRPα-CD47 axis promotes macrophage phagocytosis of exosomes derived from visceral adipose tissue and improves inflammation and metabolism in mice

Fig. 1

Diet-induced obesity affects lipid composition of AT-Exos. A Schematic diagram of AT-Exos isolation from HFD-fed or LFD-fed mice. B Representative electron microscopy images of exosomes. Scale bar, 100 nm. C The particle size of the AT-Exos measured by Nanoparticle tracking analysis. D The exosome-related protein markers CD63, HSP70 and CD9 measured by western blot in AT-Exos. These blots are representative of three independent replicate experiments. E Quantification of AT-Exos released from adipose tissue (per gram per hour) from HFD-fed and LFD-fed mice, as determined by Nanoparticle Tracking Analysis. n = 6 per group. F-I Partial Least-Squares Discriminant Analysis (PLS-DA) of lipid metabolites in AT-Exos from different origins, including WAT-Exos from HFD-fed and LFD-fed mice (panel f), BAT-Exos from HFD- and LFD-fed mice (panel g), BAT-Exos and WAT-Exos from LFD-fed mice (panel h), BAT-Exos and WAT-Exos from HFD-fed mice (panel i). J The heatmap shows relative content of different lipid types in WAT-Exos and BAT-Exos of wild-type B6 mice fed LFD or HFD for 16 weeks. n = 6 per group. All data are presented as mean ± SEM. *P < 0.05 and**P < 0.01

Back to article page