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Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease

Peroxiredoxin I (Prx I) is a member of the peroxiredoxins (Prxs) family, which are antioxidant enzymes that regulate various cellular process via intracellular oxidative signal pathways. In order to investigate the correlation between Prx I and the γ-secretase complex, which causes Alzheimer's...

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Autores principales: Lee, Young Ju, Goo, Jun Seo, Kim, Ji Eun, Nam, So Hee, Hwang, In Sik, Choi, Sun Il, Lee, Hye Ryun, Lee, Eon Phil, Choi, Hae Wook, Kim, Hong Sung, Lee, Jae Ho, Jung, Young Jin, Kim, Hak Jin, Hwang, Dae Youn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for Laboratory Animal Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251759/
https://www.ncbi.nlm.nih.gov/pubmed/22232637
http://dx.doi.org/10.5625/lar.2011.27.4.293
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author Lee, Young Ju
Goo, Jun Seo
Kim, Ji Eun
Nam, So Hee
Hwang, In Sik
Choi, Sun Il
Lee, Hye Ryun
Lee, Eon Phil
Choi, Hae Wook
Kim, Hong Sung
Lee, Jae Ho
Jung, Young Jin
Kim, Hak Jin
Hwang, Dae Youn
author_facet Lee, Young Ju
Goo, Jun Seo
Kim, Ji Eun
Nam, So Hee
Hwang, In Sik
Choi, Sun Il
Lee, Hye Ryun
Lee, Eon Phil
Choi, Hae Wook
Kim, Hong Sung
Lee, Jae Ho
Jung, Young Jin
Kim, Hak Jin
Hwang, Dae Youn
author_sort Lee, Young Ju
collection PubMed
description Peroxiredoxin I (Prx I) is a member of the peroxiredoxins (Prxs) family, which are antioxidant enzymes that regulate various cellular process via intracellular oxidative signal pathways. In order to investigate the correlation between Prx I and the γ-secretase complex, which causes Alzheimer's disease (AD), the expression level of Prx I was firstly evaluated in an animal model for AD. NSE/hPen-2 transgenic (Tg) mice, which were used as animal model in this study, showed a high level of Pen-2 expression and accumulation of Aβ-42 peptides in the hippocampus of brain. The expression level of Prx I was significantly higher on the mRNA and protein level in the brain of this model, while not change in Prx VI expression was observed. Furthermore, to verify the effect of Prx I on the γ-secretase components in vitro, the expression level of these components was analyzed in the Prx I transfectants. Of the components of the γ-secretase complex, the expression of PS-2 and Pen-2 was lower in the transfectants overexpressing Prx I compared to the vector transfectants. However, the expression of APP, NCT and APH-1 did not change in Prx I transfectants. Therefore, these results suggested that the expression of Prx I may be induced by the accumulation of Aβ-42 peptides and the overexpression of Prx I in neuroblastoma cells may regulate the expression of γ-secretase components.
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spelling pubmed-32517592012-01-09 Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease Lee, Young Ju Goo, Jun Seo Kim, Ji Eun Nam, So Hee Hwang, In Sik Choi, Sun Il Lee, Hye Ryun Lee, Eon Phil Choi, Hae Wook Kim, Hong Sung Lee, Jae Ho Jung, Young Jin Kim, Hak Jin Hwang, Dae Youn Lab Anim Res Original Article Peroxiredoxin I (Prx I) is a member of the peroxiredoxins (Prxs) family, which are antioxidant enzymes that regulate various cellular process via intracellular oxidative signal pathways. In order to investigate the correlation between Prx I and the γ-secretase complex, which causes Alzheimer's disease (AD), the expression level of Prx I was firstly evaluated in an animal model for AD. NSE/hPen-2 transgenic (Tg) mice, which were used as animal model in this study, showed a high level of Pen-2 expression and accumulation of Aβ-42 peptides in the hippocampus of brain. The expression level of Prx I was significantly higher on the mRNA and protein level in the brain of this model, while not change in Prx VI expression was observed. Furthermore, to verify the effect of Prx I on the γ-secretase components in vitro, the expression level of these components was analyzed in the Prx I transfectants. Of the components of the γ-secretase complex, the expression of PS-2 and Pen-2 was lower in the transfectants overexpressing Prx I compared to the vector transfectants. However, the expression of APP, NCT and APH-1 did not change in Prx I transfectants. Therefore, these results suggested that the expression of Prx I may be induced by the accumulation of Aβ-42 peptides and the overexpression of Prx I in neuroblastoma cells may regulate the expression of γ-secretase components. Korean Association for Laboratory Animal Science 2011-12 2011-12-19 /pmc/articles/PMC3251759/ /pubmed/22232637 http://dx.doi.org/10.5625/lar.2011.27.4.293 Text en Copyright © 2011 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Young Ju
Goo, Jun Seo
Kim, Ji Eun
Nam, So Hee
Hwang, In Sik
Choi, Sun Il
Lee, Hye Ryun
Lee, Eon Phil
Choi, Hae Wook
Kim, Hong Sung
Lee, Jae Ho
Jung, Young Jin
Kim, Hak Jin
Hwang, Dae Youn
Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title_full Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title_fullStr Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title_full_unstemmed Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title_short Peroxiredoxin I regulates the component expression of γ-secretase complex causing the Alzheimer's disease
title_sort peroxiredoxin i regulates the component expression of γ-secretase complex causing the alzheimer's disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251759/
https://www.ncbi.nlm.nih.gov/pubmed/22232637
http://dx.doi.org/10.5625/lar.2011.27.4.293
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