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Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons
Microbial flora is investigated to be related with neuropathological conditions in Alzheimer’s disease (AD), and is attracting attention as a drug discovery resource. However, the relevance between the soil microbiota and the pathological condition has not been fully clarified due to the difficulty...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891331/ https://www.ncbi.nlm.nih.gov/pubmed/35236875 http://dx.doi.org/10.1038/s41598-022-06513-z |
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author | Kondo, Takayuki Yamamoto, Tsuyoshi Okayama, Kaoru Narumi, Hideki Inoue, Haruhisa |
author_facet | Kondo, Takayuki Yamamoto, Tsuyoshi Okayama, Kaoru Narumi, Hideki Inoue, Haruhisa |
author_sort | Kondo, Takayuki |
collection | PubMed |
description | Microbial flora is investigated to be related with neuropathological conditions in Alzheimer’s disease (AD), and is attracting attention as a drug discovery resource. However, the relevance between the soil microbiota and the pathological condition has not been fully clarified due to the difficulty in isolation culture and the component complexity. In this study, we established a library of secondly metabolites produced in microorganism to investigate the potential effect of microorganisms on the production of amyloid β (Aβ), one of the most representative pathogens of AD. We conducted a library screening to quantify Aβ and neuronal toxicity by using cortical neurons from human induced pluripotent stem cells (iPSCs) of AD patients after adding secondary metabolites. Screening results and following assessment of dose-dependency identified Verrucarin A, produced in Myrothecium spp., showed 80% decrease in Aβ production. Furthermore, addition of Mer-A2026A, produced in Streptomyces pactum, showed increase in Aβ42/40 ratio at the low concentration, and decrease in Aβ production at the higher concentration. As a result, established library and iPSC-based phenotyping assay clarified a direct link between Aβ production and soil microorganisms. These results suggest that Aβ-microorganism interaction may provide insight into the AD pathophysiology with potential therapeutics. |
format | Online Article Text |
id | pubmed-8891331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88913312022-03-03 Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons Kondo, Takayuki Yamamoto, Tsuyoshi Okayama, Kaoru Narumi, Hideki Inoue, Haruhisa Sci Rep Article Microbial flora is investigated to be related with neuropathological conditions in Alzheimer’s disease (AD), and is attracting attention as a drug discovery resource. However, the relevance between the soil microbiota and the pathological condition has not been fully clarified due to the difficulty in isolation culture and the component complexity. In this study, we established a library of secondly metabolites produced in microorganism to investigate the potential effect of microorganisms on the production of amyloid β (Aβ), one of the most representative pathogens of AD. We conducted a library screening to quantify Aβ and neuronal toxicity by using cortical neurons from human induced pluripotent stem cells (iPSCs) of AD patients after adding secondary metabolites. Screening results and following assessment of dose-dependency identified Verrucarin A, produced in Myrothecium spp., showed 80% decrease in Aβ production. Furthermore, addition of Mer-A2026A, produced in Streptomyces pactum, showed increase in Aβ42/40 ratio at the low concentration, and decrease in Aβ production at the higher concentration. As a result, established library and iPSC-based phenotyping assay clarified a direct link between Aβ production and soil microorganisms. These results suggest that Aβ-microorganism interaction may provide insight into the AD pathophysiology with potential therapeutics. Nature Publishing Group UK 2022-03-02 /pmc/articles/PMC8891331/ /pubmed/35236875 http://dx.doi.org/10.1038/s41598-022-06513-z Text en © The Author(s) 2022 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 Kondo, Takayuki Yamamoto, Tsuyoshi Okayama, Kaoru Narumi, Hideki Inoue, Haruhisa Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title | Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title_full | Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title_fullStr | Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title_full_unstemmed | Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title_short | Metabolites of soil microorganisms modulate amyloid β production in Alzheimer’s neurons |
title_sort | metabolites of soil microorganisms modulate amyloid β production in alzheimer’s neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891331/ https://www.ncbi.nlm.nih.gov/pubmed/35236875 http://dx.doi.org/10.1038/s41598-022-06513-z |
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