Cedazo-Mínguez A, Popescu B O, Blanco-Millán J M, Akterin S, Pei J-J, Winblad B, Cowburn R F
Neurotec, Section for Experimental Geriatrics, Karolinska Institutet, NOVUM, KFC, plan 4, S-141 86 Huddinge, Sweden.
J Neurochem. 2003 Dec;87(5):1152-64. doi: 10.1046/j.1471-4159.2003.02088.x.
Glycogen synthase kinase-3beta (GSK-3beta) is implicated in regulating apoptosis and tau protein hyperphosphorylation in Alzheimer's disease (AD). We investigated the effects of two key AD molecules, namely apoE (E3 and E4 isoforms) and beta-amyloid (Abeta) 1-42 on GSK-3beta and its major upstream regulators, intracellular calcium and protein kinases C and B (PKC and PKB) in human SH-SY5Y neuroblastoma cells. ApoE3 induced a mild, transient, Ca2+-independent and early activation of GSK-3beta. ApoE4 effects were biphasic, with an early strong GSK-3beta activation that was partially dependent on extracellular Ca2+, followed by a GSK-3beta inactivation. ApoE4 also activated PKC-alpha and PKB possibly giving the subsequent GSK-3beta inhibition. Abeta(1-42) effects were also biphasic with a strong activation dependent partially on extracellular Ca2+ followed by an inactivation. Abeta(1-42) induced an early and potent activation of PKC-alpha and a late decrease of PKB activity. ApoE4 and Abeta(1-42) were more toxic than apoE3 as shown by MTT reduction assays and generation of activated caspase-3. ApoE4 and Abeta(1-42)-induced early activation of GSK-3beta could lead to apoptosis and tau hyperphosphorylation. A late inhibition of GSK-3beta through activation of upstream kinases likely compensates the effects of apoE4 and Abeta(1-42) on GSK-3beta, the unbalanced regulation of which may contribute to AD pathology.
糖原合酶激酶-3β(GSK-3β)与阿尔茨海默病(AD)中细胞凋亡和tau蛋白过度磷酸化的调节有关。我们研究了两种关键的AD分子,即载脂蛋白E(E3和E4亚型)和β-淀粉样蛋白(Aβ)1-42对人SH-SY5Y神经母细胞瘤细胞中GSK-3β及其主要上游调节因子细胞内钙、蛋白激酶C和B(PKC和PKB)的影响。载脂蛋白E3诱导GSK-3β轻度、短暂、不依赖Ca2+且早期激活。载脂蛋白E4的作用是双相的,早期强烈激活GSK-3β,部分依赖细胞外Ca2+,随后GSK-3β失活。载脂蛋白E4还激活PKC-α和PKB,可能导致随后的GSK-3β抑制。Aβ(1-42)的作用也是双相的,强烈激活部分依赖细胞外Ca2+,随后失活。Aβ(1-42)诱导PKC-α早期和强效激活以及PKB活性后期降低。如MTT还原试验和活化的半胱天冬酶-3的产生所示,载脂蛋白E4和Aβ(1-42)比载脂蛋白E3毒性更大。载脂蛋白E4和Aβ(1-42)诱导的GSK-3β早期激活可能导致细胞凋亡和tau过度磷酸化。通过上游激酶激活对GSK-3β的后期抑制可能补偿了载脂蛋白E4和Aβ(1-42)对GSK-3β 的影响,其调节失衡可能导致AD病理。