From the Department of Neurology and the Alzheimer's Disease Research Center and.
J Biol Chem. 2013 Nov 1;288(44):32050-63. doi: 10.1074/jbc.M113.504365. Epub 2013 Sep 19.
Recent studies link synaptojanin 1 (synj1), the main phosphoinositol (4,5)-biphosphate phosphatase (PI(4,5)P2-degrading enzyme) in the brain and synapses, to Alzheimer disease. Here we report a novel mechanism by which synj1 reversely regulates cellular clearance of amyloid-β (Aβ). Genetic down-regulation of synj1 reduces both extracellular and intracellular Aβ levels in N2a cells stably expressing the Swedish mutant of amyloid precursor protein (APP). Moreover, synj1 haploinsufficiency in an Alzheimer disease transgenic mouse model expressing the Swedish mutant APP and the presenilin-1 mutant ΔE9 reduces amyloid plaque load, as well as Aβ40 and Aβ42 levels in hippocampus of 9-month-old animals. Reduced expression of synj1 attenuates cognitive deficits in these transgenic mice. However, reduction of synj1 does not affect levels of full-length APP and the C-terminal fragment, suggesting that Aβ generation by β- and γ-secretase cleavage is not affected. Instead, synj1 knockdown increases Aβ uptake and cellular degradation through accelerated delivery to lysosomes. These effects are partially dependent upon elevated PI(4,5)P2 with synj1 down-regulation. In summary, our data suggest a novel mechanism by which reduction of a PI(4,5)P2-degrading enzyme, synj1, improves amyloid-induced neuropathology and behavior deficits through accelerating cellular Aβ clearance.
最近的研究将突触结合蛋白 1(synj1)与阿尔茨海默病联系起来,synj1 是大脑和突触中主要的磷酸肌醇(4,5)-二磷酸(PI(4,5)P2)磷酸酶(PI(4,5)P2 降解酶)。在这里,我们报告了 synj1 反向调节细胞清除淀粉样β(Aβ)的新机制。在稳定表达淀粉样前体蛋白(APP)瑞典突变体的 N2a 细胞中,synj1 的基因下调降低了细胞外和细胞内 Aβ 的水平。此外,在表达瑞典突变 APP 和早老素-1 突变体 ΔE9 的阿尔茨海默病转基因小鼠模型中,synj1 单倍不足会降低淀粉样斑块负荷,以及 9 个月大动物海马中的 Aβ40 和 Aβ42 水平。synj1 表达降低可减轻这些转基因小鼠的认知缺陷。然而,synj1 的减少并不影响全长 APP 和 C 端片段的水平,表明β-和γ-分泌酶切割产生的 Aβ不受影响。相反,synj1 敲低通过加速递送至溶酶体来增加 Aβ 的摄取和细胞降解。这些效应部分依赖于 synj1 下调时 PI(4,5)P2 的升高。总之,我们的数据表明,通过加速细胞 Aβ 清除,一种 PI(4,5)P2 降解酶 synj1 的减少改善了淀粉样蛋白诱导的神经病理学和行为缺陷的新机制。