溶酶体跨膜蛋白165通过介导溶酶体钙内流和氢离子外流来控制细胞离子稳态和细胞存活。
Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca import and H efflux.
作者信息
Chen Ran, Liu Bin, Jaślan Dawid, Kucej Lucija, Kudrina Veronika, Warnke Belinda, Klingl Yvonne E, Petrauskas Arnas, Castro Sandra Prat, Maeda Kenji, Grimm Christian, Jäättelä Marja
机构信息
Cell Death and Metabolism, Center for Autophagy, Recycling and Disease (CARD), Danish Cancer Institute, Copenhagen, Denmark.
Rare Disease, Novo Nordisk, Måløv, Denmark.
出版信息
Nat Commun. 2025 Jun 5;16(1):5209. doi: 10.1038/s41467-025-60349-5.
The proper function of lysosomes depends on their ability to store and release calcium. While several lysosomal calcium release channels have been described, how lysosomes replenish their calcium stores in placental mammals has not been determined. Using genetic depletion and overexpression techniques combined with electrophysiology and visualization of subcellular ion concentrations and their fluxes across the lysosomal membrane, we show here that TMEM165 imports calcium to the lysosomal lumen and mediates calcium-induced lysosomal proton leakage. Accordingly, TMEM165 accelerates the recovery of cells from cytosolic calcium overload thereby enhancing cell survival while causing a significant acidification of the cytosol. These data indicate that in addition to its previously identified role in the glycosylation of proteins and lipids in the Golgi, a fraction of TMEM165 localizes on the lysosomal limiting membrane, where its putative calcium/proton antiporter activity plays an essential role in the regulation of intracellular ion homeostasis and cell survival.
溶酶体的正常功能取决于它们储存和释放钙的能力。虽然已经描述了几种溶酶体钙释放通道,但胎盘哺乳动物中溶酶体如何补充其钙储存尚未确定。通过结合电生理学以及亚细胞离子浓度及其跨溶酶体膜通量的可视化的基因敲除和过表达技术,我们在此表明,跨膜蛋白165(TMEM165)将钙导入溶酶体腔并介导钙诱导的溶酶体质子泄漏。因此,TMEM165加速细胞从胞质钙超载中恢复,从而提高细胞存活率,同时导致胞质溶胶显著酸化。这些数据表明,除了其先前确定的在高尔基体中蛋白质和脂质糖基化中的作用外,一部分TMEM165定位于溶酶体限制膜上,其假定的钙/质子反向转运活性在调节细胞内离子稳态和细胞存活中起重要作用。