Increased expression of PS1 is sufficient to elevate the level and activity of γ-secretase in vivo Journal Article
| Authors: | Li, T.; Li, Y. M.; Ahn, K.; Price, D. L.; Sisodia, S. S.; Wong, P. C. |
| Article Title: | Increased expression of PS1 is sufficient to elevate the level and activity of γ-secretase in vivo |
| Abstract: | Increase in the generation and deposition of amyloid-β (Aβ) plays a central role in the development of Alzheimer's Disease (AD). Elevation of the activity of γ-secretase, a key enzyme required for the generation for Aβ, can thus be a potential risk factor in AD. However, it is not known whether γ-secretase can be upregulated in vivo. While in vitro studies showed that expression of all four components of γ-secretase (Nicastrin, Presenilin, Pen-2 and Aph-1) are required for upregulation of γ-secretase, it remains to be established as to whether this is true in vivo. To investigate whether overexpressing a single component of the γ-secretase complex is sufficient to elevate its level and activity in the brain, we analyzed transgenic mice expressing either wild type or familial AD (fAD) associated mutant PS1. In contrast to cell culture studies, overexpression of either wild type or mutant PS1 is sufficient to increase levels of Nicastrin and Pen-2, and elevate the level of active γ-secretase complex, enzymatic activity of γ-secretase and the deposition of Aβ in brains of mice. Importantly, γ-secretase comprised of mutant PS1 is less active than that of wild type PS1-containing γ-secretase; however, γ-secretase comprised of mutant PS1 cleaves at the Aβ42 site of APP-CTFs more efficiently than at the Aβ40 site, resulting in greater accumulation of Aβ deposits in the brain. Our data suggest that whereas fAD-linked PS1 mutants cause early onset disease, upregulation of PS1/γ-secretase activity may be a risk factor for late onset sporadic AD. © 2011 Li et al. |
| Keywords: | controlled study; protein expression; unclassified drug; nonhuman; mutant protein; animal cell; mouse; animal tissue; embryo; animal experiment; in vivo study; in vitro study; enzyme activity; wild type; risk factor; transgenic mouse; upregulation; enzyme assay; alzheimer disease; bioaccumulation; protein cleavage; nicastrin; regulator protein; gamma secretase; presenilin 1; presenilin 2; amyloid beta protein[1-40]; amyloid beta protein[1-42]; brain level; protein pen2 |
| Journal Title: | PLoS ONE |
| Volume: | 6 |
| Issue: | 11 |
| ISSN: | 1932-6203 |
| Publisher: | Public Library of Science |
| Date Published: | 2011-11-29 |
| Start Page: | e28179 |
| Language: | English |
| DOI: | 10.1371/journal.pone.0028179 |
| PROVIDER: | scopus |
| PMCID: | PMC3226664 |
| PUBMED: | 22140537 |
| DOI/URL: | |
| Notes: | --- - "Export Date: 3 January 2012" - "Source: Scopus" |
Altmetric
Citation Impact
BMJ Impact Analytics
Related MSK Work