Department of Neurobiology and Behavior, University of California, Irvine, 3208 Biological Sciences III, Irvine, CA 92697-4545, United States.
Brain Res. 2012 Dec 13;1489:8-16. doi: 10.1016/j.brainres.2012.10.036. Epub 2012 Oct 24.
Presenilins are necessary for calcium homeostasis and also for efficient proteolysis through the autophagy/lysosome system. Presenilin regulates both endoplasmic reticulum calcium stores and autophagic proteolysis in a γ-secretase independent fashion. The endo-lysosome system can also act as a calcium store, with calcium efflux channels being recently identified as two-pore channels 1 and 2. Here we investigated lysosomal calcium content and the channels that mediate calcium release from these acidic stores in presenilin knockout cells. We report that presenilin loss leads to a lower total lysosomal calcium store despite the buildup of lysosomes found in these cells. Additionally, we find alterations in two-pore calcium channel protein expression, with loss of presenilin preventing the formation of a high molecular weight species of TPC1 and TPC2. Finally, we find that treatments that disturb lysosomal calcium release lead to a reduction in autophagy function yet lysosomal inhibitors do not alter two-pore calcium channel expression. These data indicate that alterations in lysosomal calcium in the absence of presenilins might be leading to disruptions in autophagy.
早老素对于钙稳态和通过自噬/溶酶体系统进行有效的蛋白水解都是必需的。早老素以 γ-分泌酶非依赖性的方式调节内质网钙库和自噬性蛋白水解。内溶酶体系统也可以作为钙库,最近发现钙流出通道为双孔通道 1 和 2。在这里,我们研究了溶酶体钙含量以及在早老素敲除细胞中从这些酸性储存库释放钙的通道。我们报告说,尽管在这些细胞中发现溶酶体积累,但早老素缺失会导致总溶酶体钙库减少。此外,我们发现双孔钙通道蛋白表达发生改变,早老素缺失会阻止 TPC1 和 TPC2 的高分子量物种形成。最后,我们发现干扰溶酶体钙释放的处理会导致自噬功能降低,但溶酶体抑制剂不会改变双孔钙通道的表达。这些数据表明,早老素缺失时溶酶体钙的改变可能导致自噬的破坏。