STARD 3 mediates endoplasmic reticulum‐to‐endosome cholesterol transport at membrane contact sites

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Wilhelm, Léa, P | Wendling, Corinne | Védie, Benoît | Kobayashi, Toshihide | Chenard, Marie‐pierre | Tomasetto, Catherine | Drin, Guillaume | Alpy, Fabien

Edité par CCSD ; EMBO Press -

International audience. StAR-related lipid transfer domain-3 (STARD3) is a sterol-binding protein that creates endoplasmic reticulum (ER)-endosome contact sites. How this protein, at the crossroad between sterol uptake and synthesis pathways, impacts the intracellular distribution of this lipid was ill-defined. Here, by using in situ cholesterol labeling and quantification, we demonstrated that STARD3 induces cholesterol accumulation in endosomes at the expense of the plasma membrane. STARD3-mediated cholesterol routing depends both on its lipid transfer activity and its ability to create ER-endosome contacts. Corroborating this, in vitro reconstitution assays indicated that STARD3 and its ER-anchored partner, Vesicle-associated membrane protein-associated protein (VAP), assemble into a machine that allows a highly efficient transport of cholesterol within membrane contacts. Thus, STARD3 is a cholesterol transporter scaffolding ER-endosome contacts and modulating cellular cholesterol repartition by delivering cholesterol to endosomes.

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