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Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates

The pathogenesis of Alzheimer’s disease (AD) is primarily driven by brain accumulation of the amyloid-β-42 (Aβ(42)) peptide generated from the amyloid-β precursor protein (APP) via cleavages by β- and γ-secretase. γ-Secretase is a prime drug target for AD; however, its brain regional expression and...

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Autores principales: Xu, Yulong, Wang, Changning, Wey, Hsiao-Ying, Liang, Yingxia, Chen, Zude, Choi, Se Hoon, Ran, Chongzhao, Rynearson, Kevin D., Bernales, Daniela R., Koegel, Robert E., Fiedler, Stephanie A., Striar, Robin, Wagner, Steven L., Tanzi, Rudolph E., Zhang, Can
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553790/
https://www.ncbi.nlm.nih.gov/pubmed/32936886
http://dx.doi.org/10.1084/jem.20182266
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author Xu, Yulong
Wang, Changning
Wey, Hsiao-Ying
Liang, Yingxia
Chen, Zude
Choi, Se Hoon
Ran, Chongzhao
Rynearson, Kevin D.
Bernales, Daniela R.
Koegel, Robert E.
Fiedler, Stephanie A.
Striar, Robin
Wagner, Steven L.
Tanzi, Rudolph E.
Zhang, Can
author_facet Xu, Yulong
Wang, Changning
Wey, Hsiao-Ying
Liang, Yingxia
Chen, Zude
Choi, Se Hoon
Ran, Chongzhao
Rynearson, Kevin D.
Bernales, Daniela R.
Koegel, Robert E.
Fiedler, Stephanie A.
Striar, Robin
Wagner, Steven L.
Tanzi, Rudolph E.
Zhang, Can
author_sort Xu, Yulong
collection PubMed
description The pathogenesis of Alzheimer’s disease (AD) is primarily driven by brain accumulation of the amyloid-β-42 (Aβ(42)) peptide generated from the amyloid-β precursor protein (APP) via cleavages by β- and γ-secretase. γ-Secretase is a prime drug target for AD; however, its brain regional expression and distribution remain largely unknown. Here, we are aimed at developing molecular imaging tools for visualizing γ-secretase. We used our recently developed γ-secretase modulators (GSMs) and synthesized our GSM-based imaging agent, [(11)C]SGSM-15606. We subsequently performed molecular imaging in rodents, including AD transgenic animals, and macaques, which revealed that our probe displayed good brain uptake and selectivity, stable metabolism, and appropriate kinetics and distribution for imaging γ-secretase in the brain. Interestingly, rodents and macaques shared certain brain areas with high γ-secretase expression, suggesting a functional conservation of γ-secretase. Collectively, we have provided the first molecular brain imaging of γ-secretase, which may not only accelerate our drug discovery for AD but also advance our understanding of AD.
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spelling pubmed-75537902021-06-07 Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates Xu, Yulong Wang, Changning Wey, Hsiao-Ying Liang, Yingxia Chen, Zude Choi, Se Hoon Ran, Chongzhao Rynearson, Kevin D. Bernales, Daniela R. Koegel, Robert E. Fiedler, Stephanie A. Striar, Robin Wagner, Steven L. Tanzi, Rudolph E. Zhang, Can J Exp Med Brief Definitive Report The pathogenesis of Alzheimer’s disease (AD) is primarily driven by brain accumulation of the amyloid-β-42 (Aβ(42)) peptide generated from the amyloid-β precursor protein (APP) via cleavages by β- and γ-secretase. γ-Secretase is a prime drug target for AD; however, its brain regional expression and distribution remain largely unknown. Here, we are aimed at developing molecular imaging tools for visualizing γ-secretase. We used our recently developed γ-secretase modulators (GSMs) and synthesized our GSM-based imaging agent, [(11)C]SGSM-15606. We subsequently performed molecular imaging in rodents, including AD transgenic animals, and macaques, which revealed that our probe displayed good brain uptake and selectivity, stable metabolism, and appropriate kinetics and distribution for imaging γ-secretase in the brain. Interestingly, rodents and macaques shared certain brain areas with high γ-secretase expression, suggesting a functional conservation of γ-secretase. Collectively, we have provided the first molecular brain imaging of γ-secretase, which may not only accelerate our drug discovery for AD but also advance our understanding of AD. Rockefeller University Press 2020-09-16 /pmc/articles/PMC7553790/ /pubmed/32936886 http://dx.doi.org/10.1084/jem.20182266 Text en © 2020 Xu et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Brief Definitive Report
Xu, Yulong
Wang, Changning
Wey, Hsiao-Ying
Liang, Yingxia
Chen, Zude
Choi, Se Hoon
Ran, Chongzhao
Rynearson, Kevin D.
Bernales, Daniela R.
Koegel, Robert E.
Fiedler, Stephanie A.
Striar, Robin
Wagner, Steven L.
Tanzi, Rudolph E.
Zhang, Can
Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title_full Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title_fullStr Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title_full_unstemmed Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title_short Molecular imaging of Alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
title_sort molecular imaging of alzheimer’s disease–related gamma-secretase in mice and nonhuman primates
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553790/
https://www.ncbi.nlm.nih.gov/pubmed/32936886
http://dx.doi.org/10.1084/jem.20182266
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