Cargando…

Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium

This study aimed to identify the therapeutic ability of a novel toll-like receptor (TLR) 5 agonist, KMRC011, on ulcerative colitis induced by Citrobacter rodentium and dextran sulfate sodium in a C57BL/6N mouse model. Ulcerative colitis was induced in the mice by the oral administration of 1% dextra...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Jun-Young, Seo, Sun-Min, Kim, Han-Woong, Lee, Woo-Jong, Choi, Yang-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Microbiology and Biotechnology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895994/
https://www.ncbi.nlm.nih.gov/pubmed/36457188
http://dx.doi.org/10.4014/jmb.2209.09048
_version_ 1784881970357993472
author Kim, Jun-Young
Seo, Sun-Min
Kim, Han-Woong
Lee, Woo-Jong
Choi, Yang-Kyu
author_facet Kim, Jun-Young
Seo, Sun-Min
Kim, Han-Woong
Lee, Woo-Jong
Choi, Yang-Kyu
author_sort Kim, Jun-Young
collection PubMed
description This study aimed to identify the therapeutic ability of a novel toll-like receptor (TLR) 5 agonist, KMRC011, on ulcerative colitis induced by Citrobacter rodentium and dextran sulfate sodium in a C57BL/6N mouse model. Ulcerative colitis was induced in the mice by the oral administration of 1% dextran sulfate sodium in sterile drinking water for seven days ad libitum, followed by C. rodentium infection on the seventh day by intra-gastric administration (DSS-CT group). KMRC011 was administered intramuscularly at both 24 h and 15 min before (Treatment 1 group), and at both 15 min and 24 h after (Treatment 2 group) the C. rodentium infection. The length of the large intestine and histopathological counts were significantly greater and mucosal thickness was significantly thinner in the Treatment 1 group compared to the DSS-CT and Treatment 2 groups. Il-6 and Il-10 mRNA expression levels were upregulated, while Ifn-γ and Tnf-α mRNA expression levels were significantly downregulated in the Treatment 1 group, compared to the DSS-CT group. NF-κB p65 expression level was elevated due to ulcerative colitis in the DSS-CT group, but was significantly downregulated in the Treatment 1 group. Overall, KMRC011 showed protective effects against murine colitis by inhibiting NF-κB signaling.
format Online
Article
Text
id pubmed-9895994
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Korean Society for Microbiology and Biotechnology
record_format MEDLINE/PubMed
spelling pubmed-98959942023-02-14 Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium Kim, Jun-Young Seo, Sun-Min Kim, Han-Woong Lee, Woo-Jong Choi, Yang-Kyu J Microbiol Biotechnol Research article This study aimed to identify the therapeutic ability of a novel toll-like receptor (TLR) 5 agonist, KMRC011, on ulcerative colitis induced by Citrobacter rodentium and dextran sulfate sodium in a C57BL/6N mouse model. Ulcerative colitis was induced in the mice by the oral administration of 1% dextran sulfate sodium in sterile drinking water for seven days ad libitum, followed by C. rodentium infection on the seventh day by intra-gastric administration (DSS-CT group). KMRC011 was administered intramuscularly at both 24 h and 15 min before (Treatment 1 group), and at both 15 min and 24 h after (Treatment 2 group) the C. rodentium infection. The length of the large intestine and histopathological counts were significantly greater and mucosal thickness was significantly thinner in the Treatment 1 group compared to the DSS-CT and Treatment 2 groups. Il-6 and Il-10 mRNA expression levels were upregulated, while Ifn-γ and Tnf-α mRNA expression levels were significantly downregulated in the Treatment 1 group, compared to the DSS-CT group. NF-κB p65 expression level was elevated due to ulcerative colitis in the DSS-CT group, but was significantly downregulated in the Treatment 1 group. Overall, KMRC011 showed protective effects against murine colitis by inhibiting NF-κB signaling. The Korean Society for Microbiology and Biotechnology 2023-01-28 2022-11-15 /pmc/articles/PMC9895994/ /pubmed/36457188 http://dx.doi.org/10.4014/jmb.2209.09048 Text en Copyright © 2023 by the authors. Licensee KMB. https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research article
Kim, Jun-Young
Seo, Sun-Min
Kim, Han-Woong
Lee, Woo-Jong
Choi, Yang-Kyu
Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title_full Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title_fullStr Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title_full_unstemmed Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title_short Protective Role of the Toll-Like Receptor 5 Agonist KMRC011 against Murine Colitis Induced by Citrobacter rodentium and Dextran Sulfate Sodium
title_sort protective role of the toll-like receptor 5 agonist kmrc011 against murine colitis induced by citrobacter rodentium and dextran sulfate sodium
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895994/
https://www.ncbi.nlm.nih.gov/pubmed/36457188
http://dx.doi.org/10.4014/jmb.2209.09048
work_keys_str_mv AT kimjunyoung protectiveroleofthetolllikereceptor5agonistkmrc011againstmurinecolitisinducedbycitrobacterrodentiumanddextransulfatesodium
AT seosunmin protectiveroleofthetolllikereceptor5agonistkmrc011againstmurinecolitisinducedbycitrobacterrodentiumanddextransulfatesodium
AT kimhanwoong protectiveroleofthetolllikereceptor5agonistkmrc011againstmurinecolitisinducedbycitrobacterrodentiumanddextransulfatesodium
AT leewoojong protectiveroleofthetolllikereceptor5agonistkmrc011againstmurinecolitisinducedbycitrobacterrodentiumanddextransulfatesodium
AT choiyangkyu protectiveroleofthetolllikereceptor5agonistkmrc011againstmurinecolitisinducedbycitrobacterrodentiumanddextransulfatesodium