Crystallography, Max Delbrück Center for Molecular Medicine, 13125 Berlin, Germany;
Signal Transduction/Developmental Biology, Max Delbrück Center for Molecular Medicine, 13125 Berlin, Germany.
Proc Natl Acad Sci U S A. 2020 Mar 31;117(13):7471-7481. doi: 10.1073/pnas.1918415117. Epub 2020 Mar 13.
Eps15-homology domain containing protein 2 (EHD2) is a dynamin-related ATPase located at the neck of caveolae, but its physiological function has remained unclear. Here, we found that global genetic ablation of EHD2 in mice leads to increased lipid droplet size in fat tissue. This organismic phenotype was paralleled at the cellular level by increased fatty acid uptake via a caveolae- and CD36-dependent pathway that also involves dynamin. Concomitantly, elevated numbers of detached caveolae were found in brown and white adipose tissue lacking EHD2, and increased caveolar mobility in mouse embryonic fibroblasts. EHD2 expression itself was down-regulated in the visceral fat of two obese mouse models and obese patients. Our data suggest that EHD2 controls a cell-autonomous, caveolae-dependent fatty acid uptake pathway and imply that low EHD2 expression levels are linked to obesity.
Eps15 同源结构域蛋白 2(EHD2)是一种位于小窝颈部的与动力蛋白相关的 ATP 酶,但它的生理功能仍不清楚。在这里,我们发现 EHD2 在小鼠中的全局基因缺失导致脂肪组织中脂质滴大小增加。这种机体表型在细胞水平上与通过小窝和 CD36 依赖性途径增加脂肪酸摄取相平行,该途径还涉及动力蛋白。同时,在缺乏 EHD2 的棕色和白色脂肪组织中发现了更多分离的小窝,并且在小鼠胚胎成纤维细胞中,小窝的流动性增加。EHD2 自身的表达在两种肥胖小鼠模型和肥胖患者的内脏脂肪中下调。我们的数据表明,EHD2 控制着细胞自主的、依赖小窝的脂肪酸摄取途径,并暗示低水平的 EHD2 表达与肥胖有关。