Hepatocyte-secreted extracellular vesicles modify blood metabolome and endothelial function by an arginase-dependent mechanism

• DOI: 10.1038/srep42798
• Publication Date: 2017-02-17T10:16:02Z
• Authors: Felix Royo; Laura Moreno; Justyna Mleczko; Laura Palomo; Esperanza Gonzalez; Diana Cabrera; Angel Cogolludo; Francisco Perez V...; Sebastiaan van-Li...; Juan M. Falcon-Perez
• Keywords: Male; 0301 basic medicine; Arginase; Tetraspanin 30; Article; Acetylcholine; Rats; Tetraspanin 28; Extracellular Vesicles; 03 medical and health sciences; Blood; Hepatocytes; Animals; Metabolomics; Endothelium, Vascular; Cells, Cultured

AbstractHepatocytes release extracellular vesicles (EVs) loaded with signaling molecules and enzymes into the bloodstream. Although the importance of EVs in the intercellular communication is already recognized, the metabolic impact of the enzymes carried by these vesicles is still unclear. We evaluated the global effect of the enzymatic activities of EVs by performing untargeted metabolomic profiling of serum samples after their exposure to EVs. This approach revealed a significant change in the abundance of 94 serum metabolic signals. Our study shows that these vesicles modify the concentration of metabolites of different chemical nature including metabolites related to arginine metabolism, which regulates vascular function. To assess the functional relevance of this finding, we examined the levels of arginase-1 protein and its activity in the hepatic EVs carrying the exosomal markers CD81 and CD63. Remarkably, the arginase activity was also detected in EVs isolated from the serum in vivo, and this vesicular activity significantly increased under liver-damaging conditions. Finally, we demonstrated that EVs secreted by hepatocytes inhibited the acetylcholine-induced relaxation in isolated pulmonary arteries, via an arginase-dependent mechanism. In summary, our study demonstrates that the hepatocyte-released EVs are metabolically active, affecting a number of serum metabolites involved in oxidative stress metabolism and the endothelial function.