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AZP2006, a new promising treatment for Alzheimer’s and related diseases
Progranulin (PGRN) is a protein with multiple functions including the regulation of neuroinflammation, neuronal survival, neurite and synapsis growth. Although the mechanisms of action of PGRN are currently unknown, its potential therapeutic application in treating neurodegenerative diseases is huge...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376949/ https://www.ncbi.nlm.nih.gov/pubmed/34413330 http://dx.doi.org/10.1038/s41598-021-94708-1 |
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author | Callizot, N. Estrella, C. Burlet, S. Henriques, A. Brantis, C. Barrier, M. Campanari, M. L. Verwaerde, P. |
author_facet | Callizot, N. Estrella, C. Burlet, S. Henriques, A. Brantis, C. Barrier, M. Campanari, M. L. Verwaerde, P. |
author_sort | Callizot, N. |
collection | PubMed |
description | Progranulin (PGRN) is a protein with multiple functions including the regulation of neuroinflammation, neuronal survival, neurite and synapsis growth. Although the mechanisms of action of PGRN are currently unknown, its potential therapeutic application in treating neurodegenerative diseases is huge. Thus, strategies to increase PGRN levels in patients could provide an effective treatment. In the present study, we investigated the effects of AZP2006, a lysotropic molecule now in phase 2a clinical trial in Progressive Supranuclear Palsy patients, for its ability to increase PGRN level and promote neuroprotection. We showed for the first time the in vitro and in vivo neuroprotective effects of AZP2006 in neurons injured with Aβ(1–42) and in two different pathological animal models of Alzheimer’s disease (AD) and aging. Thus, the chronic treatment with AZP2006 was shown to reduce the loss of central synapses and neurons but also to dramatically decrease the massive neuroinflammation associated with the animal pathology. A deeper investigation showed that the beneficial effects of AZP2006 were associated with PGRN production. Also, AZP2006 binds to PSAP (the cofactor of PGRN) and inhibits TLR9 receptors normally responsible for proinflammation when activated. Altogether, these results showed the high potential of AZP2006 as a new putative treatment for AD and related diseases. |
format | Online Article Text |
id | pubmed-8376949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83769492021-08-20 AZP2006, a new promising treatment for Alzheimer’s and related diseases Callizot, N. Estrella, C. Burlet, S. Henriques, A. Brantis, C. Barrier, M. Campanari, M. L. Verwaerde, P. Sci Rep Article Progranulin (PGRN) is a protein with multiple functions including the regulation of neuroinflammation, neuronal survival, neurite and synapsis growth. Although the mechanisms of action of PGRN are currently unknown, its potential therapeutic application in treating neurodegenerative diseases is huge. Thus, strategies to increase PGRN levels in patients could provide an effective treatment. In the present study, we investigated the effects of AZP2006, a lysotropic molecule now in phase 2a clinical trial in Progressive Supranuclear Palsy patients, for its ability to increase PGRN level and promote neuroprotection. We showed for the first time the in vitro and in vivo neuroprotective effects of AZP2006 in neurons injured with Aβ(1–42) and in two different pathological animal models of Alzheimer’s disease (AD) and aging. Thus, the chronic treatment with AZP2006 was shown to reduce the loss of central synapses and neurons but also to dramatically decrease the massive neuroinflammation associated with the animal pathology. A deeper investigation showed that the beneficial effects of AZP2006 were associated with PGRN production. Also, AZP2006 binds to PSAP (the cofactor of PGRN) and inhibits TLR9 receptors normally responsible for proinflammation when activated. Altogether, these results showed the high potential of AZP2006 as a new putative treatment for AD and related diseases. Nature Publishing Group UK 2021-08-19 /pmc/articles/PMC8376949/ /pubmed/34413330 http://dx.doi.org/10.1038/s41598-021-94708-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Callizot, N. Estrella, C. Burlet, S. Henriques, A. Brantis, C. Barrier, M. Campanari, M. L. Verwaerde, P. AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title | AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title_full | AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title_fullStr | AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title_full_unstemmed | AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title_short | AZP2006, a new promising treatment for Alzheimer’s and related diseases |
title_sort | azp2006, a new promising treatment for alzheimer’s and related diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376949/ https://www.ncbi.nlm.nih.gov/pubmed/34413330 http://dx.doi.org/10.1038/s41598-021-94708-1 |
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