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Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling

H(2)O(2)-producing lactobacilli in the vaginal fluid have been suggested to play a potential tumor-preventive role in addition to the control of undesirable microorganisms. As the vaginal fluid also contains a significant concentration of peroxidase that might utilize lactobacilli-derived H(2)O(2) a...

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Autores principales: Krüger, Hannah, Bauer, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310163/
https://www.ncbi.nlm.nih.gov/pubmed/28193594
http://dx.doi.org/10.1016/j.redox.2017.01.015
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author Krüger, Hannah
Bauer, Georg
author_facet Krüger, Hannah
Bauer, Georg
author_sort Krüger, Hannah
collection PubMed
description H(2)O(2)-producing lactobacilli in the vaginal fluid have been suggested to play a potential tumor-preventive role in addition to the control of undesirable microorganisms. As the vaginal fluid also contains a significant concentration of peroxidase that might utilize lactobacilli-derived H(2)O(2) as substrate for HOCl synthesis, a dominant biological role of HOCl in both natural defence systems has been postulated. Our study shows that lactobacillus-derived H(2)O(2) per se is not likely to be beneficial for the vaginal epithelium, as it causes apoptosis nonselectively in nontransformed as well as transformed cells. However, the combination of lactobacilli and peroxidase, i.e. the situation that is actually found in vivo, leads to the conversion of H(2)O(2) to HOCl which does not affect non-malignant cells, as these do not generate extracellular superoxide anions. In contrast, malignant cells, due to their abundant extracellular superoxide anion generation allow the generation of apoptosis-inducing hydroxyl radicals through HOCl/superoxide anion interaction. In total, our data show that the combination of H(2)O(2) -generating lactobacilli and peroxidase causes the selective elimination of malignant cells and thus might contribute to the tumorpreventive potential of lactobacilli. These findings are in good agreement with epidemiological data. The contribution of lactobacilli in this system can be completely mimicked by H(2)O(2)-generating glucose oxidase, indicating that it is fully explained by bacterial generation of H(2)O(2).
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spelling pubmed-53101632017-02-21 Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling Krüger, Hannah Bauer, Georg Redox Biol Research Paper H(2)O(2)-producing lactobacilli in the vaginal fluid have been suggested to play a potential tumor-preventive role in addition to the control of undesirable microorganisms. As the vaginal fluid also contains a significant concentration of peroxidase that might utilize lactobacilli-derived H(2)O(2) as substrate for HOCl synthesis, a dominant biological role of HOCl in both natural defence systems has been postulated. Our study shows that lactobacillus-derived H(2)O(2) per se is not likely to be beneficial for the vaginal epithelium, as it causes apoptosis nonselectively in nontransformed as well as transformed cells. However, the combination of lactobacilli and peroxidase, i.e. the situation that is actually found in vivo, leads to the conversion of H(2)O(2) to HOCl which does not affect non-malignant cells, as these do not generate extracellular superoxide anions. In contrast, malignant cells, due to their abundant extracellular superoxide anion generation allow the generation of apoptosis-inducing hydroxyl radicals through HOCl/superoxide anion interaction. In total, our data show that the combination of H(2)O(2) -generating lactobacilli and peroxidase causes the selective elimination of malignant cells and thus might contribute to the tumorpreventive potential of lactobacilli. These findings are in good agreement with epidemiological data. The contribution of lactobacilli in this system can be completely mimicked by H(2)O(2)-generating glucose oxidase, indicating that it is fully explained by bacterial generation of H(2)O(2). Elsevier 2017-01-24 /pmc/articles/PMC5310163/ /pubmed/28193594 http://dx.doi.org/10.1016/j.redox.2017.01.015 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Krüger, Hannah
Bauer, Georg
Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title_full Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title_fullStr Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title_full_unstemmed Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title_short Lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
title_sort lactobacilli enhance reactive oxygen species-dependent apoptosis-inducing signaling
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310163/
https://www.ncbi.nlm.nih.gov/pubmed/28193594
http://dx.doi.org/10.1016/j.redox.2017.01.015
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