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Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity

Short-term perioperative administration of probiotics was shown to alleviate postoperative complications and promote liver recovery among patients undergoing resection for liver malignancy. The mechanisms by which probiotic bacteria effectively influence the gut microbiome composition during the per...

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Autores principales: Cohen, Shmuel J., Meyerovich, Guy, Blank, Simcha, Ovdat, Esther, Loewenstein, Shelly, Kania-Almog, Juliane, Cohen, Meir, Lahat, Guy, Klausner, Joseph M., Lubezky, Nir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234462/
https://www.ncbi.nlm.nih.gov/pubmed/37255349
http://dx.doi.org/10.1097/HC9.0000000000000164
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author Cohen, Shmuel J.
Meyerovich, Guy
Blank, Simcha
Ovdat, Esther
Loewenstein, Shelly
Kania-Almog, Juliane
Cohen, Meir
Lahat, Guy
Klausner, Joseph M.
Lubezky, Nir
author_facet Cohen, Shmuel J.
Meyerovich, Guy
Blank, Simcha
Ovdat, Esther
Loewenstein, Shelly
Kania-Almog, Juliane
Cohen, Meir
Lahat, Guy
Klausner, Joseph M.
Lubezky, Nir
author_sort Cohen, Shmuel J.
collection PubMed
description Short-term perioperative administration of probiotics was shown to alleviate postoperative complications and promote liver recovery among patients undergoing resection for liver malignancy. The mechanisms by which probiotic bacteria effectively influence the gut microbiome composition during the perioperative time are controversial. Here, we aim to elucidate the short-term direct biological effect of probiotic microbiota–derived vesicles on host liver cells during the perioperative period. METHODS: Probiotic-derived vesicles (pbMVs) were administered postoperatively. pbMVs were isolated and characterized from probiotics, mainly from the bacteria genus Lactobacillus, Bifidobacterium, and Lactococcus. Mice underwent bile duct ligation, sham laparotomy (SHAM), or 70% partial hepatectomy (70%PH). pbMVs were tracked in vivo, and intrahepatic cellular and molecular aspects were analyzed by flow cytometry and qRT-PCR techniques. Liver sinusoidal endothelial cells (LSECs) analysis for Vascular Cell Adhesion Molecule-1(VCAM-1) expression following pbMV stimulation of cultured liver non-parenchymal cells which had been activated by LPS. RESULTS: The administered pbMV rapidly translocated to the liver after surgery. pbMV administrations following surgeries enhanced neutrophil clearance; there was a dramatic decline in the liver neutrophil-to-lymphocyte ratio Ly6G(+)/CD3(+) and an increase in IL6 levels. pbMVs reduced intrahepatic VCAM1 and ICAM2 expression compared with control following SHAM and decrease in IL10 levels following 70%PH. The administration of pbMV improved liver regeneration 72 hours following surgical liver resection with a significant decrease in IL17 expression. pbMVs modulated VCAM-1 on liver sinusoidal endothelial cells in liver cell culture. CONCLUSIONS: Our study findings provide mechanistic insights into the liver-gut axis following surgery and illustrate how probiotic vesicles can reduce adhesion molecule expression and affect immune cell invasion and liver immunity, resulting in improved liver recovery following hepatic surgery.
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spelling pubmed-102344622023-06-02 Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity Cohen, Shmuel J. Meyerovich, Guy Blank, Simcha Ovdat, Esther Loewenstein, Shelly Kania-Almog, Juliane Cohen, Meir Lahat, Guy Klausner, Joseph M. Lubezky, Nir Hepatol Commun Original Article Short-term perioperative administration of probiotics was shown to alleviate postoperative complications and promote liver recovery among patients undergoing resection for liver malignancy. The mechanisms by which probiotic bacteria effectively influence the gut microbiome composition during the perioperative time are controversial. Here, we aim to elucidate the short-term direct biological effect of probiotic microbiota–derived vesicles on host liver cells during the perioperative period. METHODS: Probiotic-derived vesicles (pbMVs) were administered postoperatively. pbMVs were isolated and characterized from probiotics, mainly from the bacteria genus Lactobacillus, Bifidobacterium, and Lactococcus. Mice underwent bile duct ligation, sham laparotomy (SHAM), or 70% partial hepatectomy (70%PH). pbMVs were tracked in vivo, and intrahepatic cellular and molecular aspects were analyzed by flow cytometry and qRT-PCR techniques. Liver sinusoidal endothelial cells (LSECs) analysis for Vascular Cell Adhesion Molecule-1(VCAM-1) expression following pbMV stimulation of cultured liver non-parenchymal cells which had been activated by LPS. RESULTS: The administered pbMV rapidly translocated to the liver after surgery. pbMV administrations following surgeries enhanced neutrophil clearance; there was a dramatic decline in the liver neutrophil-to-lymphocyte ratio Ly6G(+)/CD3(+) and an increase in IL6 levels. pbMVs reduced intrahepatic VCAM1 and ICAM2 expression compared with control following SHAM and decrease in IL10 levels following 70%PH. The administration of pbMV improved liver regeneration 72 hours following surgical liver resection with a significant decrease in IL17 expression. pbMVs modulated VCAM-1 on liver sinusoidal endothelial cells in liver cell culture. CONCLUSIONS: Our study findings provide mechanistic insights into the liver-gut axis following surgery and illustrate how probiotic vesicles can reduce adhesion molecule expression and affect immune cell invasion and liver immunity, resulting in improved liver recovery following hepatic surgery. Lippincott Williams & Wilkins 2023-05-31 /pmc/articles/PMC10234462/ /pubmed/37255349 http://dx.doi.org/10.1097/HC9.0000000000000164 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
Cohen, Shmuel J.
Meyerovich, Guy
Blank, Simcha
Ovdat, Esther
Loewenstein, Shelly
Kania-Almog, Juliane
Cohen, Meir
Lahat, Guy
Klausner, Joseph M.
Lubezky, Nir
Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title_full Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title_fullStr Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title_full_unstemmed Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title_short Microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
title_sort microbiota transfer following liver surgery involves microbial extracellular vesicle migration that affects liver immunity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234462/
https://www.ncbi.nlm.nih.gov/pubmed/37255349
http://dx.doi.org/10.1097/HC9.0000000000000164
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