Endothelial cell CD36 regulates membrane ceramide formation, exosome fatty acid transfer and circulating fatty acid levels

• Published in: Nature communications Vol. 14; no. 1; p. 4029
• Main Authors: Peche, V. S., Pietka, T. A., Jacome-Sosa, M., Samovski, D., Palacios, H., Chatterjee-Basu, G., Dudley, A. C., Beatty, W., Meyer, G. A., Goldberg, I. J., Abumrad, N. A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 07-07-2023; Nature Publishing Group; Nature Portfolio
• Subjects: 13/1; 13/106; 14; 14/19; 14/28; 14/63; 38; 38/39; 38/91; 631/45/287/1183; 631/80/128/1276; 631/80/86/2365; Actin; Animals; Blood circulation; Blood vessels; Caveolae; Caveolin; Caveolin-1; CD36 antigen; CD36 Antigens - genetics; CD36 Antigens - metabolism; CD63 antigen; Cell interactions; Ceramide; Ceramides - metabolism; Endocytosis; Endothelial cells; Endothelial Cells - metabolism; Endothelium; Exosomes - metabolism; Fatty acids; Fatty Acids - metabolism; Humanities and Social Sciences; Membranes; Mice; multidisciplinary; Muscle Fibers, Skeletal - metabolism; Muscles; Myotubes; Parenchyma; Phenotypes; Phosphorylation; Science; Science (multidisciplinary); Tyrosine; Vesicles
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-39752-3

Endothelial cell (EC) CD36 controls tissue fatty acid (FA) uptake. Here we examine how ECs transfer FAs. FA interaction with apical membrane CD36 induces Src phosphorylation of caveolin-1 tyrosine-14 (Cav-1Y14) and ceramide generation in caveolae. Ensuing fission of caveolae yields vesicles containing FAs, CD36 and ceramide that are secreted basolaterally as small (80–100 nm) exosome-like extracellular vesicles (sEVs). We visualize in transwells EC transfer of FAs in sEVs to underlying myotubes. In mice with EC-expression of the exosome marker emeraldGFP-CD63, muscle fibers accumulate circulating FAs in emGFP-labeled puncta. The FA-sEV pathway is mapped through its suppression by CD36 depletion, blocking actin-remodeling, Src inhibition, Cav-1Y14 mutation, and neutral sphingomyelinase 2 inhibition. Suppression of sEV formation in mice reduces muscle FA uptake, raises circulating FAs, which remain in blood vessels, and lowers glucose, mimicking prominent
Cd36
−/
−
mice phenotypes. The findings show that FA uptake influences membrane ceramide, endocytosis, and EC communication with parenchymal cells.
Endothelial cell CD36 controls tissue fatty acid uptake. Here the authors show how fatty acid uptake by endothelial cells involves regulation of membrane ceramide production, caveolae dynamics, and exosome generation, these events facilitate transfer of circulating fatty acids to tissues and communication between endothelium and parenchyma.