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. 3 | Cell Communication and Signaling

Fig. 3

From: Physiological and pathological consequences of exosomes at the blood–brain-barrier interface

Fig. 3

Exos can cross the BBB interface using paracellular and transcellular pathways. Due to the existence of transferrin on the Exo surface, these nanoparticles can attach to the transferrin receptor (TFR) at the luminal surface of brain ECs, leading to the formation of clathrin-coated pits and Exo internalization. The internalized Exos are direct to lysosomal degradation where the released cargo can regulate specific signaling pathways inside the ECs or cross the endothelial barrier and exist through the abluminal surface. After the production of inflammatory cytokines and certain physiological conditions, Exos can cross the BBB via a paracellular route where the function of tight junctions is not abnormal. Reprinted with permission [1], Copyright 2021. Cell & Bioscience

Back to article page