Please use this identifier to cite or link to this item:
Title: Pin1 has opposite effects on wild-type and P301L tau stability and tauopathy
Authors: Lim, J.
Balastik, M.
Lee, T.H.
Nakamura, K.
Liou, Y.-C. 
Sun, A.
Finn, G.
Pastorino, L.
Lee, V.M.-Y.
Lu, K.P.
Issue Date: 1-May-2008
Citation: Lim, J., Balastik, M., Lee, T.H., Nakamura, K., Liou, Y.-C., Sun, A., Finn, G., Pastorino, L., Lee, V.M.-Y., Lu, K.P. (2008-05-01). Pin1 has opposite effects on wild-type and P301L tau stability and tauopathy. Journal of Clinical Investigation 118 (5) : 1877-1889. ScholarBank@NUS Repository.
Abstract: Tau pathology is a hallmark of many neurodegenerative diseases including Alzheimer disease (AD) and frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17). Genetic tau mutations can cause FTDP-17, and mice overexpressing tau mutants such as P301L tau are used as AD models. However, since no tau mutations are found in AD, it remains unclear how appropriate tau mutant mice are as an AD model. The prolyl isomerase Pin1 binds and isomerizes tau and has been implicated in protecting against neurodegeneration, but whether such Pin1 regulation is affected by tau mutations is unknown. Consistent with earlier findings that Pin1 KO induces tauopathy, here we demonstrate that Pin1 knockdown or KO increased WT tau protein stability in vitro and in mice and that Pin1 overexpression suppressed the tauopathy phenotype in WT tau transgenic mice. Unexpectedly, Pin1 knockdown or KO decreased P301L tau protein stability and abolished its robust tauopathy phenotype in mice. In contrast, Pin1 overexpression exacerbated the tauopathy phenotype in P301L tau mice. Thus, Pin1 has opposite effects on the tauopathy phenotype depending on whether the tau is WT or a P301L mutant, indicating the need for disease-specific therapies for tauopathies.
Source Title: Journal of Clinical Investigation
ISSN: 00219738
DOI: 10.1172/JCI34308
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.


checked on Apr 9, 2021


checked on Apr 1, 2021

Page view(s)

checked on Apr 11, 2021

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.