Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783544527262318592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7284693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT limdaejin lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT kimheekyung lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT jeongjaeho lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT jungyoonseok lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT leesheeeun lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT jangheechang lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT jungsookin lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT choihuengsik lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT rheejoonhaeng lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT leesunggwon lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT parkchungoo lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT songmiryoung lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis AT choyhyone lipocalin2inducedbybacterialflagellinprotectsmiceagainstcyclophosphamidemediatedneutropenicsepsis |