1. Academic Validation
  2. Polyphyllin I attenuates cognitive impairments and reduces AD-like pathology through CIP2A-PP2A signaling pathway in 3XTg-AD mice

Polyphyllin I attenuates cognitive impairments and reduces AD-like pathology through CIP2A-PP2A signaling pathway in 3XTg-AD mice

  • FASEB J. 2020 Dec;34(12):16414-16431. doi: 10.1096/fj.202001499R.
Ying Zhou 1 2 Dichen Yang 3 Hao Chen 3 Chenfei Zheng 1 Huanchang Jiang 3 Xiaoyuan Liu 3 Xingzhou Huang 4 Simin Ye 3 Shuangshuang Song 3 Nan Jiang 3 Zhongyuan Zhao 3 Shuqing Ma 3 Jun Ma 5 Kate Huang 5 Chaosheng Chen 1 Xiaofang Fan 6 Yongsheng Gong 6 Xiaochuan Wang 7 Junming Fan 6 Rong Liu 7 Yangping Shentu 2 5
Affiliations

Affiliations

  • 1 Department of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • 2 Key Laboratory of Diagnosis and Treatment of Severe Hepato-Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • 3 Wenzhou Medical University, Wenzhou, China.
  • 4 Central laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • 5 Department of Pathology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • 6 Institute of Hypoxia Medicine, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.
  • 7 Department of Pathophysiology, Key Laboratory of Ministry of Education for Neurological Disorders, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Abstract

Polyphyllin I (PPI) is a natural phytochemical drug isolated from Plants which can inhibit the proliferation of Cancer cells. One of the PPI tumor-inhibitory effects is through downregulating the expression of Cancerous Inhibitor of PP2A (CIP2A), the latter, is found upregulated in Alzheimer's disease (AD) brains and participates in the development of AD. In this study, we explored the application of PPI in experimental AD treatment in CIP2A-overexpressed cells and 3XTg-AD mice. In CIP2A-overexpressed HEK293 cells or primary neurons, PPI effectively reduced CIP2A level, activated PP2A, and decreased the phosphorylation of tau/APP and the level of Aβ. Furthermore, synaptic protein levels were restored by PPI in primary neurons overexpressing CIP2A. Animal experiments in 3XTg-AD mice revealed that PPI treatment resulted in decreased CIP2A expression and PP2A re-activation. With the modification of CIP2A-PP2A signaling, the hyperphosphorylation of tau/APP and Aβ overproduction were prevented, and the cognitive impairments of 3XTg-AD mice were rescued. In summary, PPI ameliorated AD-like pathology and cognitive impairment through modulating CIP2A-PP2A signaling pathway. It may be a potential drug candidate for the treatment of AD.

Keywords

cancerous inhibitor of PP2A (CIP2A); cognitive impairments; polyphyllin I (PPI).

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