Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.

Alzheimer's disease (AD) is tightly correlated with synapse loss in vulnerable brain regions. It is assumed that specific molecular entities such as Aβ and tau cause synapse loss in AD, yet unbiased screens for synaptotoxic activities have not been performed. Here, we performed size exclusion c...

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Autores principales:	Hao Jiang, Thomas J Esparza, Terrance T Kummer, David L Brody
Formato:	article
Lenguaje:	EN
Publicado:	Public Library of Science (PLoS) 2021
Materias:	Medicine R Science Q
Acceso en línea:	https://doaj.org/article/022bb368d84f4c268f73494fc6f10c44
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spelling	oai:doaj.org-article:022bb368d84f4c268f73494fc6f10c442021-12-02T20:05:57ZUnbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.1932-620310.1371/journal.pone.0259335https://doaj.org/article/022bb368d84f4c268f73494fc6f10c442021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0259335https://doaj.org/toc/1932-6203Alzheimer's disease (AD) is tightly correlated with synapse loss in vulnerable brain regions. It is assumed that specific molecular entities such as Aβ and tau cause synapse loss in AD, yet unbiased screens for synaptotoxic activities have not been performed. Here, we performed size exclusion chromatography on soluble human brain homogenates from AD cases, high pathology non-demented controls, and low pathology age-matched controls using our novel high content primary cultured neuron-based screening assay. Both presynaptic and postsynaptic toxicities were elevated in homogenates from AD cases and high pathology non-demented controls to a similar extent, with more modest synaptotoxic activities in homogenates from low pathology normal controls. Surprisingly, synaptotoxic activities were found in size fractions peaking between the 17-44 kDa size standards that did not match well with Aβ and tau immunoreactive species in these homogenates. The fractions containing previously identified high molecular weight soluble amyloid beta aggregates/"oligomers" were non-toxic in this assay. Furthermore, immunodepletion of Aβ and tau did not reduce synaptotoxic activity. This result contrasts with previous findings involving the same methods applied to 3xTg-AD mouse brain extracts. The nature of the synaptotoxic species has not been identified. Overall, our data indicates one or more potential Aβ and tau independent synaptotoxic activities in human AD brain homogenates. This result aligns well with the key role of synaptic loss in the early cognitive decline and may provide new insight into AD pathophysiology.Hao JiangThomas J EsparzaTerrance T KummerDavid L BrodyPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11, p e0259335 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	Medicine R Science Q
spellingShingle	Medicine R Science Q Hao Jiang Thomas J Esparza Terrance T Kummer David L Brody Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
description	Alzheimer's disease (AD) is tightly correlated with synapse loss in vulnerable brain regions. It is assumed that specific molecular entities such as Aβ and tau cause synapse loss in AD, yet unbiased screens for synaptotoxic activities have not been performed. Here, we performed size exclusion chromatography on soluble human brain homogenates from AD cases, high pathology non-demented controls, and low pathology age-matched controls using our novel high content primary cultured neuron-based screening assay. Both presynaptic and postsynaptic toxicities were elevated in homogenates from AD cases and high pathology non-demented controls to a similar extent, with more modest synaptotoxic activities in homogenates from low pathology normal controls. Surprisingly, synaptotoxic activities were found in size fractions peaking between the 17-44 kDa size standards that did not match well with Aβ and tau immunoreactive species in these homogenates. The fractions containing previously identified high molecular weight soluble amyloid beta aggregates/"oligomers" were non-toxic in this assay. Furthermore, immunodepletion of Aβ and tau did not reduce synaptotoxic activity. This result contrasts with previous findings involving the same methods applied to 3xTg-AD mouse brain extracts. The nature of the synaptotoxic species has not been identified. Overall, our data indicates one or more potential Aβ and tau independent synaptotoxic activities in human AD brain homogenates. This result aligns well with the key role of synaptic loss in the early cognitive decline and may provide new insight into AD pathophysiology.
format	article
author	Hao Jiang Thomas J Esparza Terrance T Kummer David L Brody
author_facet	Hao Jiang Thomas J Esparza Terrance T Kummer David L Brody
author_sort	Hao Jiang
title	Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
title_short	Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
title_full	Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
title_fullStr	Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
title_full_unstemmed	Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.
title_sort	unbiased high-content screening reveals aβ- and tau-independent synaptotoxic activities in human brain homogenates from alzheimer's patients and high-pathology controls.
publisher	Public Library of Science (PLoS)
publishDate	2021
url	https://doaj.org/article/022bb368d84f4c268f73494fc6f10c44
work_keys_str_mv	AT haojiang unbiasedhighcontentscreeningrevealsabandtauindependentsynaptotoxicactivitiesinhumanbrainhomogenatesfromalzheimerspatientsandhighpathologycontrols AT thomasjesparza unbiasedhighcontentscreeningrevealsabandtauindependentsynaptotoxicactivitiesinhumanbrainhomogenatesfromalzheimerspatientsandhighpathologycontrols AT terrancetkummer unbiasedhighcontentscreeningrevealsabandtauindependentsynaptotoxicactivitiesinhumanbrainhomogenatesfromalzheimerspatientsandhighpathologycontrols AT davidlbrody unbiasedhighcontentscreeningrevealsabandtauindependentsynaptotoxicactivitiesinhumanbrainhomogenatesfromalzheimerspatientsandhighpathologycontrols
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Unbiased high-content screening reveals Aβ- and tau-independent synaptotoxic activities in human brain homogenates from Alzheimer's patients and high-pathology controls.

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