Zhang Qing, Xia Yiyuan, Luo Hongbin, Huang Sheng, Wang Yongjun, Shentu Yangping, Mahaman Yacoubou Abdoul Razak, Huang Fang, Ke Dan, Wang Qun, Liu Rong, Wang Jian-Zhi, Zhang Bin, Wang Xiaochuan
Department of Pathophysiology, School of Basic Medicine, Key Laboratory of Ministry of Education for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Medical College, Hubei University for Nationalities, Enshi, China.
Front Mol Neurosci. 2018 Nov 27;11:437. doi: 10.3389/fnmol.2018.00437. eCollection 2018.
polysaccharide (CPPs), a natural products with potentially lower toxicity and better bioavailability has been used in traditional Chinese medicine for 1000s of years and a neuroprotective polysaccharide mitigates tau pathology in Alzheimer's disease (AD) mouse model. However, whether CPPs can relieve AD pathology and cognitive defects remains poorly understood. Here we reported that CPPs remarkably increased the cell viability and PP2A activity, decreased tau phosphorylation in HEK 293/tau cells. Next, we employed an adeno-associated virus serotype 2 (AAV2)-induced expression of human full length tau (hTau) in C57/BL6 mice to mimic AD tau pathology. One month intragastric administration of CPPs significantly increased PP2A activity and reduced tau phosphorylation at Ser199, Ser202/Thr205 (AT8) and Thr231 in hippocampus of AAV2-hTau infected mice. Furthermore, behavioral tests revealed that CPPs rescued hTau overexpression induced cognitive defects while CPPs significantly increased the fEPSP slope and synaptic proteins including synaptotagmin and synaptophysin. Together, our data suggest that CPPs might prevent AD-like tau hyperphosphorylation via activation of PP2A and attenuates AD-like cognitive impairments through restoring the synaptic plasticity and synaptogenesis. In conclusion, our findings suggest that CPPs might be a potential candidate compound for the treatment of tau related diseases.
多糖(CPPs)是一种潜在毒性较低且生物利用度较好的天然产物,已在传统中药中使用了数千年,一种具有神经保护作用的多糖可减轻阿尔茨海默病(AD)小鼠模型中的tau病理变化。然而,CPPs是否能缓解AD病理变化和认知缺陷仍知之甚少。在此我们报告,CPPs显著提高了HEK 293/tau细胞的细胞活力和PP2A活性,降低了tau磷酸化水平。接下来,我们利用腺相关病毒2型(AAV2)诱导C57/BL6小鼠表达人全长tau(hTau),以模拟AD tau病理变化。对AAV2-hTau感染小鼠进行为期一个月的胃内给予CPPs,可显著提高PP2A活性,并降低海马体中Ser199、Ser202/Thr205(AT8)和Thr231位点的tau磷酸化水平。此外,行为测试表明,CPPs可挽救hTau过表达诱导的认知缺陷,同时CPPs显著增加了场兴奋性突触后电位(fEPSP)斜率以及包括突触结合蛋白和突触素在内的突触蛋白。总之,我们的数据表明,CPPs可能通过激活PP2A来预防类似AD的tau过度磷酸化,并通过恢复突触可塑性和突触形成来减轻类似AD的认知障碍。综上所述,我们的研究结果表明,CPPs可能是治疗tau相关疾病的潜在候选化合物。