College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.
Department of Histology and Embryology, China Medical University, Shenyang 110122, China.
Int J Mol Sci. 2021 Oct 27;22(21):11582. doi: 10.3390/ijms222111582.
Hydrogen peroxide (HO)-induced neuronal apoptosis is critical to the pathology of Alzheimer's disease (AD) as well as other neurodegenerative diseases. The neuroprotective effects of apolipoprotein (ApoE) isoforms against apoptosis and the underlying mechanism remains controversial. Here, we have generated human cortical neurons from iPSCs and induced apoptosis with HO. We show that ApoE2 and ApoE3 pretreatments significantly attenuate neuronal apoptosis, whereas ApoE4 has no neuroprotective effect and higher concentrations of ApoE4 even display toxic effect. We further identify that ApoE2 and ApoE3 regulate Akt/FoxO3a/Bim signaling pathway in the presence of HO. We propose that ApoE alleviates HO-induced apoptosis in human iPSC-derived neuronal culture in an isoform specific manner. Our results provide an alternative mechanistic explanation on how ApoE isoforms influence the risk of AD onset as well as a promising therapeutic target for diseases involving neuronal apoptosis in the central nervous system.
过氧化氢(HO)诱导的神经元凋亡是阿尔茨海默病(AD)以及其他神经退行性疾病病理学的关键。载脂蛋白(ApoE)异构体对细胞凋亡的神经保护作用及其潜在机制仍存在争议。在这里,我们用人诱导多能干细胞(iPSC)生成皮质神经元,并使用 HO 诱导其凋亡。我们发现 ApoE2 和 ApoE3 预处理可显著减轻神经元凋亡,而 ApoE4 则没有神经保护作用,且较高浓度的 ApoE4 甚至显示出毒性作用。我们进一步发现,在 HO 存在的情况下,ApoE2 和 ApoE3 调节 Akt/FoxO3a/Bim 信号通路。我们提出,ApoE 以异构体特异性方式减轻人 iPSC 源性神经元培养物中 HO 诱导的凋亡。我们的结果为 ApoE 异构体如何影响 AD 发病风险提供了另一种机制解释,也为涉及中枢神经系统神经元凋亡的疾病提供了有前途的治疗靶点。