کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6264067 1613950 2012 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research ReportPresenilin-null cells have altered two-pore calcium channel expression and lysosomal calcium: Implications for lysosomal function
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Research ReportPresenilin-null cells have altered two-pore calcium channel expression and lysosomal calcium: Implications for lysosomal function
چکیده انگلیسی

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.

► Presenilin loss leads a reduction in overall lysosomal calcium content. ► Presenilins regulate expression of two-pore lysosomal calcium channels. ► Inhibition of lysosomal calcium channels decreases autophagic function. ► Thus, presenilin regulation of lysosomal calcium modulates autophagy.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1489, 13 December 2012, Pages 8-16
نویسندگان
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