Liu Rong, Wang Jian-Zhi
Department of Pathophysiology, Hubei Provincial Key Laboratory of Neurological Diseases, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China.
Pathophysiology. 2009 Oct;16(4):273-7. doi: 10.1016/j.pathophys.2009.02.008. Epub 2009 Mar 10.
Protein phosphatase 2A (PP2A) is the predominant serine/threonine phosphatase in eukaryotic cells. In Alzheimer's disease (AD), PP2A activity is decreased. Decreased PP2A activity is suggested to be involved in NFT formation and neurodegeneration. PP2A is also involved in APP secreting pathway, thus probably participating the Abeta production. Based on our research and other previous findings, decreased PP2Ac level, decreased PP2A holoenzyme composition, increased level of PP2A inhibitors, increased PP2Ac Leu309 demethylation and Tyr307 phosphorylation could partly explain the mechanisms of PP2A inactivation in AD. Abeta over-production, estrogen deficiency and impaired homocysteine metabolism are the possible up-stream factors that inactivate PP2A in AD neurons. Further studies are needed to disclose the role of PP2A in Alzheimer's disease.
蛋白磷酸酶2A(PP2A)是真核细胞中主要的丝氨酸/苏氨酸磷酸酶。在阿尔茨海默病(AD)中,PP2A活性降低。PP2A活性降低被认为与神经原纤维缠结(NFT)形成和神经退行性变有关。PP2A也参与淀粉样前体蛋白(APP)分泌途径,因此可能参与β淀粉样蛋白(Aβ)的产生。基于我们的研究和其他先前的发现,PP2Ac水平降低、PP2A全酶组成减少、PP2A抑制剂水平升高、PP2Ac亮氨酸309去甲基化和酪氨酸307磷酸化增加可能部分解释了AD中PP2A失活的机制。Aβ产生过多、雌激素缺乏和同型半胱氨酸代谢受损是AD神经元中使PP2A失活的可能上游因素。需要进一步研究以揭示PP2A在阿尔茨海默病中的作用。