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Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis

Neutropenic sepsis is a fatal consequence of chemotherapy, and septic complications are the principal cause of mortality. Chemotherapy-induced neutropenia leads to the formation of microscopic ulcers in the gastrointestinal epithelium that function as a portal of entry for intraluminal bacteria, whi...

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Autores principales: Lim, Daejin, Kim, Hee Kyung, Jeong, Jae-Ho, Jung, Yoon Seok, Lee, Shee Eun, Jang, Hee-Chang, Jung, Sook-In, Choi, Hueng-Sik, Rhee, Joon Haeng, Lee, Sung-Gwon, Park, Chungoo, Song, Miryoung, Choy, Hyon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284693/
https://www.ncbi.nlm.nih.gov/pubmed/32365611
http://dx.doi.org/10.3390/microorganisms8050646
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author Lim, Daejin
Kim, Hee Kyung
Jeong, Jae-Ho
Jung, Yoon Seok
Lee, Shee Eun
Jang, Hee-Chang
Jung, Sook-In
Choi, Hueng-Sik
Rhee, Joon Haeng
Lee, Sung-Gwon
Park, Chungoo
Song, Miryoung
Choy, Hyon E.
author_facet Lim, Daejin
Kim, Hee Kyung
Jeong, Jae-Ho
Jung, Yoon Seok
Lee, Shee Eun
Jang, Hee-Chang
Jung, Sook-In
Choi, Hueng-Sik
Rhee, Joon Haeng
Lee, Sung-Gwon
Park, Chungoo
Song, Miryoung
Choy, Hyon E.
author_sort Lim, Daejin
collection PubMed
description Neutropenic sepsis is a fatal consequence of chemotherapy, and septic complications are the principal cause of mortality. Chemotherapy-induced neutropenia leads to the formation of microscopic ulcers in the gastrointestinal epithelium that function as a portal of entry for intraluminal bacteria, which translocate across the intestinal mucosal barrier and gain access to systemic sites, causing septicemia. A cyclophosphamide-induced mouse model was developed to mimic the pathophysiologic sequence of events that occurs in patients with neutropenic sepsis. The TLR5 agonist bacterial flagellin derived from Vibrio vulnificus extended the survival of cyclophosphamide-treated mice by reducing the bacterial load in internal organs. The protective effect of flagellin was mediated by the antimicrobial protein lipocalin 2 (Lcn2), which is induced by TLR5-NF-κB activation in hepatocytes. Lcn2 sequestered iron from infecting bacteria, particularly siderophore enterobactin-dependent members of the Enterobacteriaceae family, thereby limiting their proliferation. Lcn2 should be considered for the treatment of neutropenic sepsis and gastrointestinal damage during chemotherapy to prevent or minimize the adverse effects of cancer chemotherapy.
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spelling pubmed-72846932020-06-15 Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis Lim, Daejin Kim, Hee Kyung Jeong, Jae-Ho Jung, Yoon Seok Lee, Shee Eun Jang, Hee-Chang Jung, Sook-In Choi, Hueng-Sik Rhee, Joon Haeng Lee, Sung-Gwon Park, Chungoo Song, Miryoung Choy, Hyon E. Microorganisms Article Neutropenic sepsis is a fatal consequence of chemotherapy, and septic complications are the principal cause of mortality. Chemotherapy-induced neutropenia leads to the formation of microscopic ulcers in the gastrointestinal epithelium that function as a portal of entry for intraluminal bacteria, which translocate across the intestinal mucosal barrier and gain access to systemic sites, causing septicemia. A cyclophosphamide-induced mouse model was developed to mimic the pathophysiologic sequence of events that occurs in patients with neutropenic sepsis. The TLR5 agonist bacterial flagellin derived from Vibrio vulnificus extended the survival of cyclophosphamide-treated mice by reducing the bacterial load in internal organs. The protective effect of flagellin was mediated by the antimicrobial protein lipocalin 2 (Lcn2), which is induced by TLR5-NF-κB activation in hepatocytes. Lcn2 sequestered iron from infecting bacteria, particularly siderophore enterobactin-dependent members of the Enterobacteriaceae family, thereby limiting their proliferation. Lcn2 should be considered for the treatment of neutropenic sepsis and gastrointestinal damage during chemotherapy to prevent or minimize the adverse effects of cancer chemotherapy. MDPI 2020-04-29 /pmc/articles/PMC7284693/ /pubmed/32365611 http://dx.doi.org/10.3390/microorganisms8050646 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lim, Daejin
Kim, Hee Kyung
Jeong, Jae-Ho
Jung, Yoon Seok
Lee, Shee Eun
Jang, Hee-Chang
Jung, Sook-In
Choi, Hueng-Sik
Rhee, Joon Haeng
Lee, Sung-Gwon
Park, Chungoo
Song, Miryoung
Choy, Hyon E.
Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title_full Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title_fullStr Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title_full_unstemmed Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title_short Lipocalin2 Induced by Bacterial Flagellin Protects Mice against Cyclophosphamide Mediated Neutropenic Sepsis
title_sort lipocalin2 induced by bacterial flagellin protects mice against cyclophosphamide mediated neutropenic sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284693/
https://www.ncbi.nlm.nih.gov/pubmed/32365611
http://dx.doi.org/10.3390/microorganisms8050646
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