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Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells

Examining how host cells affect metabolic behaviors of probiotics is pivotal to better understand the mechanisms underlying the probiotic efficacy in vivo. However, studies to elucidate the interaction between probiotics and host cells, such as intestinal epithelial cells, remain limited. Therefore,...

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Autores principales: Sen, Akira, Nishimura, Tatsuki, Yoshimoto, Shin, Yoshida, Keisuke, Gotoh, Aina, Katoh, Toshihiko, Yoneda, Yasuko, Hashimoto, Toyoyuki, Xiao, Jin-Zhong, Katayama, Takane, Odamaki, Toshitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133457/
https://www.ncbi.nlm.nih.gov/pubmed/37125172
http://dx.doi.org/10.3389/fmicb.2023.1155438
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author Sen, Akira
Nishimura, Tatsuki
Yoshimoto, Shin
Yoshida, Keisuke
Gotoh, Aina
Katoh, Toshihiko
Yoneda, Yasuko
Hashimoto, Toyoyuki
Xiao, Jin-Zhong
Katayama, Takane
Odamaki, Toshitaka
author_facet Sen, Akira
Nishimura, Tatsuki
Yoshimoto, Shin
Yoshida, Keisuke
Gotoh, Aina
Katoh, Toshihiko
Yoneda, Yasuko
Hashimoto, Toyoyuki
Xiao, Jin-Zhong
Katayama, Takane
Odamaki, Toshitaka
author_sort Sen, Akira
collection PubMed
description Examining how host cells affect metabolic behaviors of probiotics is pivotal to better understand the mechanisms underlying the probiotic efficacy in vivo. However, studies to elucidate the interaction between probiotics and host cells, such as intestinal epithelial cells, remain limited. Therefore, in this study, we performed a comprehensive metabolome analysis of a co-culture containing Bifidobacterium breve MCC1274 and induced pluripotent stem cells (iPS)-derived small intestinal-like cells. In the co-culture, we observed a significant increase in several amino acid metabolites, including indole-3-lactic acid (ILA) and phenyllactic acid (PLA). In accordance with the metabolic shift, the expression of genes involved in ILA synthesis, such as transaminase and tryptophan synthesis-related genes, was also elevated in B. breve MCC1274 cells. ILA production was enhanced in the presence of purines, which were possibly produced by intestinal epithelial cells (IECs). These findings suggest a synergistic action of probiotics and IECs, which may represent a molecular basis of host-probiotic interaction in vivo.
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spelling pubmed-101334572023-04-28 Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells Sen, Akira Nishimura, Tatsuki Yoshimoto, Shin Yoshida, Keisuke Gotoh, Aina Katoh, Toshihiko Yoneda, Yasuko Hashimoto, Toyoyuki Xiao, Jin-Zhong Katayama, Takane Odamaki, Toshitaka Front Microbiol Microbiology Examining how host cells affect metabolic behaviors of probiotics is pivotal to better understand the mechanisms underlying the probiotic efficacy in vivo. However, studies to elucidate the interaction between probiotics and host cells, such as intestinal epithelial cells, remain limited. Therefore, in this study, we performed a comprehensive metabolome analysis of a co-culture containing Bifidobacterium breve MCC1274 and induced pluripotent stem cells (iPS)-derived small intestinal-like cells. In the co-culture, we observed a significant increase in several amino acid metabolites, including indole-3-lactic acid (ILA) and phenyllactic acid (PLA). In accordance with the metabolic shift, the expression of genes involved in ILA synthesis, such as transaminase and tryptophan synthesis-related genes, was also elevated in B. breve MCC1274 cells. ILA production was enhanced in the presence of purines, which were possibly produced by intestinal epithelial cells (IECs). These findings suggest a synergistic action of probiotics and IECs, which may represent a molecular basis of host-probiotic interaction in vivo. Frontiers Media S.A. 2023-04-13 /pmc/articles/PMC10133457/ /pubmed/37125172 http://dx.doi.org/10.3389/fmicb.2023.1155438 Text en Copyright © 2023 Sen, Nishimura, Yoshimoto, Yoshida, Gotoh, Katoh, Yoneda, Hashimoto, Xiao, Katayama and Odamaki. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sen, Akira
Nishimura, Tatsuki
Yoshimoto, Shin
Yoshida, Keisuke
Gotoh, Aina
Katoh, Toshihiko
Yoneda, Yasuko
Hashimoto, Toyoyuki
Xiao, Jin-Zhong
Katayama, Takane
Odamaki, Toshitaka
Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title_full Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title_fullStr Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title_full_unstemmed Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title_short Comprehensive analysis of metabolites produced by co-cultivation of Bifidobacterium breve MCC1274 with human iPS-derived intestinal epithelial cells
title_sort comprehensive analysis of metabolites produced by co-cultivation of bifidobacterium breve mcc1274 with human ips-derived intestinal epithelial cells
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133457/
https://www.ncbi.nlm.nih.gov/pubmed/37125172
http://dx.doi.org/10.3389/fmicb.2023.1155438
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