BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells

<p>Abstract</p> <p>Background</p> <p>Accumulation of amyloid β-peptide (Aβ) in the plaques is one of the major pathological features in Alzheimer's disease (AD). Sequential cleavage of amyloid precursor protein (APP) by β-site APP cleaving enzyme 1 (BACE-1) and γ-s...

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Main Authors: Edlund Michael, Belda Oscar, Jämsä Anne, Lindström Erik
Format: Article
Language:English
Published: BMC 2011-10-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/18/1/76
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spelling doaj-65c9b8c818e64305bc1b7f6d49193f462020-11-25T00:26:06ZengBMCJournal of Biomedical Science1021-77701423-01272011-10-011817610.1186/1423-0127-18-76BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cellsEdlund MichaelBelda OscarJämsä AnneLindström Erik<p>Abstract</p> <p>Background</p> <p>Accumulation of amyloid β-peptide (Aβ) in the plaques is one of the major pathological features in Alzheimer's disease (AD). Sequential cleavage of amyloid precursor protein (APP) by β-site APP cleaving enzyme 1 (BACE-1) and γ-secretase results in the formation of Aβ peptides. Preventing Aβ formation is believed to attenuate AD progression and BACE-1 and γ-secretase are thus attractive targets for AD drug development.</p> <p>Methods</p> <p>Combining BACE-1 and γ-secretase inhibition on Aβ secretion from human neuroblastoma SH-SY5Y cells was evaluated in this study. Secreted Aβ40 and Aβ42 levels were measured from SH-SY5Y cells stably transfected with APPwt or APPswe genes. A selective BACE inhibitor and the γ-secretase inhibitor LY450139 (semagacestat) were used to inhibit respective secretase.</p> <p>Results</p> <p>LY450139 increased Aβ40 and Aβ42 secretion from SH-SY5Y APPwt cells at low concentrations (by 60% at 3 nM) followed by subsequent inhibition at higher concentrations (IC<sub>50 </sub>90 nM). Washout studies showed that the Aβ increase evoked by 3 nM LY450139 was not due to enhanced cleavage following substrate accumulation but rather to activation of Aβ formation. By contrast, LY450139 inhibited Aβ formation from SH-SY5Y APPswe in a monophasic manner (IC<sub>50 </sub>18 nM). The BACE inhibitor <it>per se </it>inhibited Aβ secretion from both SH-SY5Y APPwt and SH-SY5Y APPswe cells with IC<sub>50</sub>s ranging between 7 - 18 nM and also prevented the increased Aβ secretion evoked by 3 nM LY450139. Combining the BACE inhibitor with higher inhibitory concentrations of LY450139 failed to demonstrate any clear additive or synergistic effects.</p> <p>Conclusion</p> <p>BACE-1 inhibition attenuates the Aβ increase evoked by LY450139 while not providing any obvious synergistic effects on LY450139-mediated inhibition.</p> http://www.jbiomedsci.com/content/18/1/76
collection DOAJ
language English
format Article
sources DOAJ
author Edlund Michael
Belda Oscar
Jämsä Anne
Lindström Erik
spellingShingle Edlund Michael
Belda Oscar
Jämsä Anne
Lindström Erik
BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
Journal of Biomedical Science
author_facet Edlund Michael
Belda Oscar
Jämsä Anne
Lindström Erik
author_sort Edlund Michael
title BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
title_short BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
title_full BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
title_fullStr BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
title_full_unstemmed BACE-1 inhibition prevents the γ-secretase inhibitor evoked Aβ rise in human neuroblastoma SH-SY5Y cells
title_sort bace-1 inhibition prevents the γ-secretase inhibitor evoked aβ rise in human neuroblastoma sh-sy5y cells
publisher BMC
series Journal of Biomedical Science
issn 1021-7770
1423-0127
publishDate 2011-10-01
description <p>Abstract</p> <p>Background</p> <p>Accumulation of amyloid β-peptide (Aβ) in the plaques is one of the major pathological features in Alzheimer's disease (AD). Sequential cleavage of amyloid precursor protein (APP) by β-site APP cleaving enzyme 1 (BACE-1) and γ-secretase results in the formation of Aβ peptides. Preventing Aβ formation is believed to attenuate AD progression and BACE-1 and γ-secretase are thus attractive targets for AD drug development.</p> <p>Methods</p> <p>Combining BACE-1 and γ-secretase inhibition on Aβ secretion from human neuroblastoma SH-SY5Y cells was evaluated in this study. Secreted Aβ40 and Aβ42 levels were measured from SH-SY5Y cells stably transfected with APPwt or APPswe genes. A selective BACE inhibitor and the γ-secretase inhibitor LY450139 (semagacestat) were used to inhibit respective secretase.</p> <p>Results</p> <p>LY450139 increased Aβ40 and Aβ42 secretion from SH-SY5Y APPwt cells at low concentrations (by 60% at 3 nM) followed by subsequent inhibition at higher concentrations (IC<sub>50 </sub>90 nM). Washout studies showed that the Aβ increase evoked by 3 nM LY450139 was not due to enhanced cleavage following substrate accumulation but rather to activation of Aβ formation. By contrast, LY450139 inhibited Aβ formation from SH-SY5Y APPswe in a monophasic manner (IC<sub>50 </sub>18 nM). The BACE inhibitor <it>per se </it>inhibited Aβ secretion from both SH-SY5Y APPwt and SH-SY5Y APPswe cells with IC<sub>50</sub>s ranging between 7 - 18 nM and also prevented the increased Aβ secretion evoked by 3 nM LY450139. Combining the BACE inhibitor with higher inhibitory concentrations of LY450139 failed to demonstrate any clear additive or synergistic effects.</p> <p>Conclusion</p> <p>BACE-1 inhibition attenuates the Aβ increase evoked by LY450139 while not providing any obvious synergistic effects on LY450139-mediated inhibition.</p>
url http://www.jbiomedsci.com/content/18/1/76
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