Neurobiology of Disease Laboratory, Genetics and Aging Research Unit, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
Neurosci Lett. 2010 Dec 10;486(2):68-72. doi: 10.1016/j.neulet.2010.08.048. Epub 2010 Sep 15.
BACE1 and presenilin (PS)/γ-secretase are primary proteolytic enzymes responsible for the generation of pathogenic amyloid β-peptides (Aβ) in Alzheimer's disease. We and others have found that β-subunits of the voltage-gated sodium channel (Na(v)βs) also undergo sequential proteolytic cleavages mediated by BACE1 and PS/γ-secretase. In a follow-up study, we reported that elevated BACE1 activity regulates total and surface expression of voltage-gated sodium channels (Na(v)1 channels) and thereby modulates sodium currents in neuronal cells and mouse brains. In this review, we focus on the molecular mechanism of how BACE1 and PS/γ-secretase regulate Na(v)1 channels in neuronal cells. We will also discuss potential physiological and pathological roles of BACE1- and PS/γ-secretase-mediated processing of Na(v)βs in relation to Na(v)1 channel function.
BACE1 和早老素(PS)/γ-分泌酶是负责阿尔茨海默病中致病性淀粉样 β-肽(Aβ)产生的主要蛋白水解酶。我们和其他人发现,电压门控钠离子通道(Na(v)βs)的β亚基也通过 BACE1 和 PS/γ-分泌酶进行连续的蛋白水解切割。在后续研究中,我们报告说,升高的 BACE1 活性调节电压门控钠离子通道(Na(v)1 通道)的总表达和表面表达,从而调节神经元细胞和小鼠大脑中的钠离子电流。在这篇综述中,我们重点讨论了 BACE1 和 PS/γ-分泌酶如何调节神经元细胞中 Na(v)1 通道的分子机制。我们还将讨论 BACE1 和 PS/γ-分泌酶介导的 Na(v)βs 加工与 Na(v)1 通道功能相关的潜在生理和病理作用。