The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells

Neurodegenerative disorders, including Tauopathies that involve tau protein, base their pathological mechanism on forming proteinaceous aggregates, which has a deleterious effect on cells triggering an inflammatory response. Moreover, tau inhibitors can exert their mechanism of action through noncov...

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Published in:Molecules
Main Authors: González, Camila, Cartagena, Constanza, Caballero, Leonardo, Melo, Francisco, Areche Medina, Carlos Alberto, Cornejo, Alberto
Format: Article in Journal/Newspaper
Language:English
Published: MDPI 2021
Subjects:
Online Access:https://doi.org/10.3390/molecules26123760
https://repositorio.uchile.cl/handle/2250/182873
id ftunivchile:oai:repositorio.uchile.cl:2250/182873
record_format openpolar
spelling ftunivchile:oai:repositorio.uchile.cl:2250/182873 2023-05-15T13:38:36+02:00 The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells González, Camila Cartagena, Constanza Caballero, Leonardo Melo, Francisco Areche Medina, Carlos Alberto Cornejo, Alberto 2021 application/pdf https://doi.org/10.3390/molecules26123760 https://repositorio.uchile.cl/handle/2250/182873 en eng MDPI Molecules 2021, 26, 3760. doi:10.3390/molecules26123760 https://repositorio.uchile.cl/handle/2250/182873 Attribution-NonCommercial-NoDerivs 3.0 United States http://creativecommons.org/licenses/by-nc-nd/3.0/us/ CC-BY-NC-ND Molecules Lichens Tauopathies Alpha,beta carbonyl group Inhibitors Aggregates Cytotoxicity Artículo de revista 2021 ftunivchile https://doi.org/10.3390/molecules26123760 2021-11-28T00:49:53Z Neurodegenerative disorders, including Tauopathies that involve tau protein, base their pathological mechanism on forming proteinaceous aggregates, which has a deleterious effect on cells triggering an inflammatory response. Moreover, tau inhibitors can exert their mechanism of action through noncovalent and covalent interactions. Thus, Michael’s addition appears as a feasible type of interaction involving an , unsaturated carbonyl moiety to avoid pathological confirmation and further cytotoxicity. Moreover, we isolated three compounds from Antarctic lichens Cladonia cariosa and Himantormia lugubris: protolichesterinic acid (1), fumarprotocetraric acid (2), and lichesterinic acid (3). The maleimide cysteine labeling assay showed that compounds 1, 2, and 3 inhibit at 50 M, but compounds 2 and 3 are statistically significant. Based on its inhibition capacity, we decided to test compound 2 further. Thus, our results suggest that compound 2 remodel soluble oligomers and diminish sheet content, as demonstrated through ThT experiments. Hence, we added externally treated oligomers with compound 2 to demonstrate that they are harmless in cell culture. First, the morphology of cells in the presence of aggregates does not suffer evident changes compared to the control. Additionally, the externally added aggregates do not provoke a substantial LDH release compared to the control, indicating that treated oligomers do not provoke membrane damage in cell culture compared with aggregates alone. Thus, in the present work, we demonstrated that Michael’s acceptors found in lichens could serve as a scaffold to explore different mechanisms of action to turn tau aggregates into harmless species. Instituto Antartico Chileno (INACH) RT_18-19 ANID-Chile Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 1201013 Fondequip EQM 130149 EQM 170111 Dicyt-Usach 041831MH Versión publicada - versión final del editor Article in Journal/Newspaper Antarc* Antarctic antartic* Instituto Antartico Chileno Universidad de Chile: Repositorio académico Antarctic Inach ENVELOPE(-60.783,-60.783,-62.467,-62.467) Molecules 26 12 3760
institution Open Polar
collection Universidad de Chile: Repositorio académico
op_collection_id ftunivchile
language English
topic Lichens
Tauopathies
Alpha,beta carbonyl group
Inhibitors
Aggregates
Cytotoxicity
spellingShingle Lichens
Tauopathies
Alpha,beta carbonyl group
Inhibitors
Aggregates
Cytotoxicity
González, Camila
Cartagena, Constanza
Caballero, Leonardo
Melo, Francisco
Areche Medina, Carlos Alberto
Cornejo, Alberto
The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
topic_facet Lichens
Tauopathies
Alpha,beta carbonyl group
Inhibitors
Aggregates
Cytotoxicity
description Neurodegenerative disorders, including Tauopathies that involve tau protein, base their pathological mechanism on forming proteinaceous aggregates, which has a deleterious effect on cells triggering an inflammatory response. Moreover, tau inhibitors can exert their mechanism of action through noncovalent and covalent interactions. Thus, Michael’s addition appears as a feasible type of interaction involving an , unsaturated carbonyl moiety to avoid pathological confirmation and further cytotoxicity. Moreover, we isolated three compounds from Antarctic lichens Cladonia cariosa and Himantormia lugubris: protolichesterinic acid (1), fumarprotocetraric acid (2), and lichesterinic acid (3). The maleimide cysteine labeling assay showed that compounds 1, 2, and 3 inhibit at 50 M, but compounds 2 and 3 are statistically significant. Based on its inhibition capacity, we decided to test compound 2 further. Thus, our results suggest that compound 2 remodel soluble oligomers and diminish sheet content, as demonstrated through ThT experiments. Hence, we added externally treated oligomers with compound 2 to demonstrate that they are harmless in cell culture. First, the morphology of cells in the presence of aggregates does not suffer evident changes compared to the control. Additionally, the externally added aggregates do not provoke a substantial LDH release compared to the control, indicating that treated oligomers do not provoke membrane damage in cell culture compared with aggregates alone. Thus, in the present work, we demonstrated that Michael’s acceptors found in lichens could serve as a scaffold to explore different mechanisms of action to turn tau aggregates into harmless species. Instituto Antartico Chileno (INACH) RT_18-19 ANID-Chile Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 1201013 Fondequip EQM 130149 EQM 170111 Dicyt-Usach 041831MH Versión publicada - versión final del editor
format Article in Journal/Newspaper
author González, Camila
Cartagena, Constanza
Caballero, Leonardo
Melo, Francisco
Areche Medina, Carlos Alberto
Cornejo, Alberto
author_facet González, Camila
Cartagena, Constanza
Caballero, Leonardo
Melo, Francisco
Areche Medina, Carlos Alberto
Cornejo, Alberto
author_sort González, Camila
title The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
title_short The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
title_full The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
title_fullStr The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
title_full_unstemmed The fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
title_sort fumarprotocetraric acid inhibits tau covalently, avoiding cytotoxicity of aggregates in cells
publisher MDPI
publishDate 2021
url https://doi.org/10.3390/molecules26123760
https://repositorio.uchile.cl/handle/2250/182873
long_lat ENVELOPE(-60.783,-60.783,-62.467,-62.467)
geographic Antarctic
Inach
geographic_facet Antarctic
Inach
genre Antarc*
Antarctic
antartic*
Instituto Antartico Chileno
genre_facet Antarc*
Antarctic
antartic*
Instituto Antartico Chileno
op_source Molecules
op_relation Molecules 2021, 26, 3760.
doi:10.3390/molecules26123760
https://repositorio.uchile.cl/handle/2250/182873
op_rights Attribution-NonCommercial-NoDerivs 3.0 United States
http://creativecommons.org/licenses/by-nc-nd/3.0/us/
op_rightsnorm CC-BY-NC-ND
op_doi https://doi.org/10.3390/molecules26123760
container_title Molecules
container_volume 26
container_issue 12
container_start_page 3760
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