Zack Stephanie R, Nikolaienko Roman, Cook Ben, Melki Ronald, Zima Aleksey V, Campbell Edward M
Loyola University Chicago.
Institut Francois Jacob (MIRCen), CEA, CNRS, Fontenay-aux-Roses.
Res Sq. 2023 Jan 27:rs.3.rs-2508369. doi: 10.21203/rs.3.rs-2508369/v1.
Altered expression of vacuole membrane protein 1 (VMP1) has recently been observed in the context of multiple sclerosis and Parkinson's disease (PD). However, how changes in VMP1 expression may impact pathogenesis has not been explored. Here, we report that genetic deletion of VMP1 from a monocytic cell line resulted in increased NLRP3 inflammasome activation and release of proinflammatory molecules. Examination of the VMP1 dependent changes in these cells revealed that VMP1 deficiency led to decreased SERCA activity and increased intracellular [Ca]. We also observed calcium overload in mitochondria in VMP1 depleted cells, which was associated with mitochondrial dysfunction and release of mitochondrial DNA into the cytoplasm and the extracellular environment. Autophagic defects were also observed in VMP1 depleted macrophages. Collectively, these studies reveal VMP1 as a negative regulator of inflammatory responses, and we postulate that decreased expression of VMP1 can aggravate the inflammatory sequelae associated with neurodegenerative diseases like PD.
最近在多发性硬化症和帕金森病(PD)的背景下观察到液泡膜蛋白1(VMP1)的表达改变。然而,VMP1表达的变化如何影响发病机制尚未得到探索。在这里,我们报告从单核细胞系中基因删除VMP1导致NLRP3炎性小体激活增加和促炎分子释放。对这些细胞中VMP1依赖性变化的检查表明,VMP1缺乏导致SERCA活性降低和细胞内[Ca]增加。我们还观察到VMP1缺失细胞中线粒体钙超载,这与线粒体功能障碍以及线粒体DNA释放到细胞质和细胞外环境有关。在VMP1缺失的巨噬细胞中也观察到自噬缺陷。总的来说,这些研究揭示了VMP1是炎症反应的负调节因子,并且我们推测VMP1表达降低会加重与PD等神经退行性疾病相关的炎症后遗症。