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Biological function of Presenilin and its role in AD pathogenesis
Presenilins (PSs) are the catalytic core of γ-secretase complex. However, the mechanism of FAD-associated PS mutations in AD pathogenesis still remains elusive. Here we review the general biology and mechanism of γ-secretase and focus on the catalytic components – presenilins and their biological fu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718700/ https://www.ncbi.nlm.nih.gov/pubmed/23866842 http://dx.doi.org/10.1186/2047-9158-2-15 |
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author | Zhang, Shuting Zhang, Mingming Cai, Fang Song, Weihong |
author_facet | Zhang, Shuting Zhang, Mingming Cai, Fang Song, Weihong |
author_sort | Zhang, Shuting |
collection | PubMed |
description | Presenilins (PSs) are the catalytic core of γ-secretase complex. However, the mechanism of FAD-associated PS mutations in AD pathogenesis still remains elusive. Here we review the general biology and mechanism of γ-secretase and focus on the catalytic components – presenilins and their biological functions and contributions to the AD pathogenesis. The functions of presenilins are divided into γ-secretase dependent and γ-secretase independent ones. The γ-secretase dependent functions of presenilins are exemplified by the sequential cleavages in the processing of APP and Notch; the γ-secretase independent functions of presenilins include stabilizing β-catenin in Wnt signaling pathway, regulating calcium homeostasis and their interaction with synaptic transmission. |
format | Online Article Text |
id | pubmed-3718700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37187002013-07-23 Biological function of Presenilin and its role in AD pathogenesis Zhang, Shuting Zhang, Mingming Cai, Fang Song, Weihong Transl Neurodegener Review Presenilins (PSs) are the catalytic core of γ-secretase complex. However, the mechanism of FAD-associated PS mutations in AD pathogenesis still remains elusive. Here we review the general biology and mechanism of γ-secretase and focus on the catalytic components – presenilins and their biological functions and contributions to the AD pathogenesis. The functions of presenilins are divided into γ-secretase dependent and γ-secretase independent ones. The γ-secretase dependent functions of presenilins are exemplified by the sequential cleavages in the processing of APP and Notch; the γ-secretase independent functions of presenilins include stabilizing β-catenin in Wnt signaling pathway, regulating calcium homeostasis and their interaction with synaptic transmission. BioMed Central 2013-07-17 /pmc/articles/PMC3718700/ /pubmed/23866842 http://dx.doi.org/10.1186/2047-9158-2-15 Text en Copyright © 2013 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Zhang, Shuting Zhang, Mingming Cai, Fang Song, Weihong Biological function of Presenilin and its role in AD pathogenesis |
title | Biological function of Presenilin and its role in AD pathogenesis |
title_full | Biological function of Presenilin and its role in AD pathogenesis |
title_fullStr | Biological function of Presenilin and its role in AD pathogenesis |
title_full_unstemmed | Biological function of Presenilin and its role in AD pathogenesis |
title_short | Biological function of Presenilin and its role in AD pathogenesis |
title_sort | biological function of presenilin and its role in ad pathogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718700/ https://www.ncbi.nlm.nih.gov/pubmed/23866842 http://dx.doi.org/10.1186/2047-9158-2-15 |
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