Molecular Role of Protein Phosphatases in Alzheimer’s and Other Neurodegenerative Diseases

Author:

Hassan Mubashir1,Yasir Muhammad2,Shahzadi Saba1,Chun Wanjoo2ORCID,Kloczkowski Andrzej134ORCID

Affiliation:

1. The Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children’s Hospital, Columbus, OH 43205, USA

2. Department of Pharmacology, Kangwon National University School of Medicine, Chuncheon 24341, Republic of Korea

3. Department of Pediatrics, The Ohio State University, Columbus, OH 43205, USA

4. Department of Biomedical Informatics, The Ohio State University, Columbus, OH 43210, USA

Abstract

Alzheimer’s disease (AD) is distinguished by the gradual loss of cognitive function, which is associated with neuronal loss and death. Accumulating evidence supports that protein phosphatases (PPs; PP1, PP2A, PP2B, PP4, PP5, PP6, and PP7) are directly linked with amyloid beta (Aβ) as well as the formation of the neurofibrillary tangles (NFTs) causing AD. Published data reported lower PP1 and PP2A activity in both gray and white matters in AD brains than in the controls, which clearly shows that dysfunctional phosphatases play a significant role in AD. Moreover, PP2A is also a major causing factor of AD through the deregulation of the tau protein. Here, we review recent advances on the role of protein phosphatases in the pathology of AD and other neurodegenerative diseases. A better understanding of this problem may lead to the development of phosphatase-targeted therapies for neurodegenerative disorders in the near future.

Funder

National Institutes of Health

Publisher

MDPI AG

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