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Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production
Cancer patients often experience impairments in cognitive function. However, the evidence for tumor-mediated neurological impairment and detailed mechanisms are still lacking. Gut microbiota has been demonstrated to be involved in the immune system homeostasis and brain functions. Here we find that...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318068/ https://www.ncbi.nlm.nih.gov/pubmed/37400621 http://dx.doi.org/10.1038/s42003-023-05036-1 |
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author | Zhu, Ying Mei, Yu Baby, Nimmi Teo, Huey Yee Binte Hanafi, Zuhairah Mohd Salleh, Siti Nazihah Sajikumar, Sreedharan Liu, Haiyan |
author_facet | Zhu, Ying Mei, Yu Baby, Nimmi Teo, Huey Yee Binte Hanafi, Zuhairah Mohd Salleh, Siti Nazihah Sajikumar, Sreedharan Liu, Haiyan |
author_sort | Zhu, Ying |
collection | PubMed |
description | Cancer patients often experience impairments in cognitive function. However, the evidence for tumor-mediated neurological impairment and detailed mechanisms are still lacking. Gut microbiota has been demonstrated to be involved in the immune system homeostasis and brain functions. Here we find that hepatocellular carcinoma (HCC) growth alters the gut microbiota and impedes the cognitive functions. The synaptic tagging and capture (STC), an associative cellular mechanism for the formation of associative memory, is impaired in the tumor-bearing mice. STC expression is rescued after microbiota sterilization. Transplantation of microbiota from HCC tumor-bearing mice induces similar STC impairment in wide type mice. Mechanistic study reveals that HCC growth significantly elevates the serum and hippocampus IL-1β levels. IL-1β depletion in the HCC tumor-bearing mice restores the STC. Taken together, these results demonstrate that gut microbiota plays a crucial role in mediating the tumor-induced impairment of the cognitive function via upregulating IL-1β production. |
format | Online Article Text |
id | pubmed-10318068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103180682023-07-05 Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production Zhu, Ying Mei, Yu Baby, Nimmi Teo, Huey Yee Binte Hanafi, Zuhairah Mohd Salleh, Siti Nazihah Sajikumar, Sreedharan Liu, Haiyan Commun Biol Article Cancer patients often experience impairments in cognitive function. However, the evidence for tumor-mediated neurological impairment and detailed mechanisms are still lacking. Gut microbiota has been demonstrated to be involved in the immune system homeostasis and brain functions. Here we find that hepatocellular carcinoma (HCC) growth alters the gut microbiota and impedes the cognitive functions. The synaptic tagging and capture (STC), an associative cellular mechanism for the formation of associative memory, is impaired in the tumor-bearing mice. STC expression is rescued after microbiota sterilization. Transplantation of microbiota from HCC tumor-bearing mice induces similar STC impairment in wide type mice. Mechanistic study reveals that HCC growth significantly elevates the serum and hippocampus IL-1β levels. IL-1β depletion in the HCC tumor-bearing mice restores the STC. Taken together, these results demonstrate that gut microbiota plays a crucial role in mediating the tumor-induced impairment of the cognitive function via upregulating IL-1β production. Nature Publishing Group UK 2023-07-03 /pmc/articles/PMC10318068/ /pubmed/37400621 http://dx.doi.org/10.1038/s42003-023-05036-1 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhu, Ying Mei, Yu Baby, Nimmi Teo, Huey Yee Binte Hanafi, Zuhairah Mohd Salleh, Siti Nazihah Sajikumar, Sreedharan Liu, Haiyan Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title | Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title_full | Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title_fullStr | Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title_full_unstemmed | Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title_short | Tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal CA1 area via IL-1β production |
title_sort | tumor-mediated microbiota alteration impairs synaptic tagging/capture in the hippocampal ca1 area via il-1β production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318068/ https://www.ncbi.nlm.nih.gov/pubmed/37400621 http://dx.doi.org/10.1038/s42003-023-05036-1 |
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