Yamada Seiya, Ogawa Hayato, Funato Miona, Kato Misaki, Nakadate Kazuhiko, Mizukoshi Tomoya, Kawakami Kiyoharu, Kobayashi Ryosuke, Horii Takuro, Hatada Izuho, Sakakibara Shin-Ichi
Laboratory for Molecular Neurobiology, Faculty of Human Sciences, Waseda University, Tokorozawa, Saitama, Japan.
Neuroscience Center, HiLIFE-Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Commun Biol. 2025 Mar 11;8(1):348. doi: 10.1038/s42003-025-07717-5.
Endoplasmic reticulum (ER) stores Ca and plays crucial roles in protein folding, lipid transfer, and it's perturbations trigger an ER stress. In the liver, chronic ER stress is involved in the pathogenesis of metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH). Dysfunction of sarco/endoplasmic reticulum calcium ATPase (SERCA2), a key regulator of Ca transport from the cytosol to ER, is associated with the induction of ER stress and lipid droplet formation. We previously identified NACHT and WD repeat domain-containing protein 1 (Nwd1) localized at the ER and mitochondria. However, the physiological significance of Nwd1 outside the brain remains unclear. In this study, we revealed that Nwd1 mice exhibited pathological manifestations comparable to MASH. Nwd1 interacts with SERCA2 near ER membranes. Nwd1 livers exhibited reduced SERCA2 ATPase activity and a smaller Ca pool in the ER, leading to an exacerbated state of ER stress. These findings highlight the importance of SERCA2 activity mediated by Nwd1 in the pathogenesis of MASH.
内质网(ER)储存钙离子,并在蛋白质折叠、脂质转运中发挥关键作用,其功能紊乱会引发内质网应激。在肝脏中,慢性内质网应激参与代谢功能障碍相关脂肪性肝病(MASLD)和代谢功能障碍相关脂肪性肝炎(MASH)的发病机制。肌浆网/内质网钙ATP酶(SERCA2)是将钙离子从细胞质转运至内质网的关键调节因子,其功能障碍与内质网应激的诱导及脂滴形成有关。我们之前鉴定出含NACHT和WD重复结构域蛋白1(Nwd1)定位于内质网和线粒体。然而,Nwd1在脑外的生理意义仍不清楚。在本研究中,我们发现Nwd1基因敲除小鼠表现出与MASH相似的病理表现。Nwd1在内质网膜附近与SERCA2相互作用。Nwd1基因敲除小鼠的肝脏SERCA2 ATP酶活性降低,内质网中的钙池较小,导致内质网应激加剧。这些发现凸显了由Nwd1介导的SERCA2活性在MASH发病机制中的重要性。