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The hepatic innate immune response is lobe-specific in a murine model endotoxemia
The liver plays a central role in the innate immune response to endotoxemia. While previous studies have demonstrated lobe-specific transcriptional responses to various insults, whether this is true in response to endotoxemia is unknown. We sought to assess whether there were significant intra- and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784545/ https://www.ncbi.nlm.nih.gov/pubmed/30774009 http://dx.doi.org/10.1177/1753425918823900 |
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author | Nguyen, Leanna Sandoval, Jeryl De Dios, Robyn Yihdego, Elesa Zarate, Miguel Castro, Odalis McKenna, Sarah Wright, Clyde J |
author_facet | Nguyen, Leanna Sandoval, Jeryl De Dios, Robyn Yihdego, Elesa Zarate, Miguel Castro, Odalis McKenna, Sarah Wright, Clyde J |
author_sort | Nguyen, Leanna |
collection | PubMed |
description | The liver plays a central role in the innate immune response to endotoxemia. While previous studies have demonstrated lobe-specific transcriptional responses to various insults, whether this is true in response to endotoxemia is unknown. We sought to assess whether there were significant intra- and inter-lobe differences in the murine hepatic innate immune transcriptional response to endotoxemia. Adult male ICR mice were exposed to i.p. LPS (5 mg/kg, 30 min, 60 min, 5 h) and primary (Tnf, Cxcl1, Nfkbia, Tnfiap3) and secondary (Il6, Nos2) innate immune response gene expression was assessed in the left medial, right medial, left lateral, and right lateral lobes, and the papillary and caudate processes. The expression of all innate immune response genes increased following i.p. LPS challenge. When tested at the early time points (30 and 60 min), the left medial lobe and caudate process consistently demonstrated the highest induction of gene expression. Most inter-lobe differences were attenuated at later time points (5 h). To improve reproducibility of the study of endotoxemia induced by i.p. LPS challenge, inclusion of appropriate methodological details regarding collection of hepatic tissue should be included when reporting scientific results in published manuscripts. |
format | Online Article Text |
id | pubmed-6784545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67845452019-10-09 The hepatic innate immune response is lobe-specific in a murine model endotoxemia Nguyen, Leanna Sandoval, Jeryl De Dios, Robyn Yihdego, Elesa Zarate, Miguel Castro, Odalis McKenna, Sarah Wright, Clyde J Innate Immun Original Articles The liver plays a central role in the innate immune response to endotoxemia. While previous studies have demonstrated lobe-specific transcriptional responses to various insults, whether this is true in response to endotoxemia is unknown. We sought to assess whether there were significant intra- and inter-lobe differences in the murine hepatic innate immune transcriptional response to endotoxemia. Adult male ICR mice were exposed to i.p. LPS (5 mg/kg, 30 min, 60 min, 5 h) and primary (Tnf, Cxcl1, Nfkbia, Tnfiap3) and secondary (Il6, Nos2) innate immune response gene expression was assessed in the left medial, right medial, left lateral, and right lateral lobes, and the papillary and caudate processes. The expression of all innate immune response genes increased following i.p. LPS challenge. When tested at the early time points (30 and 60 min), the left medial lobe and caudate process consistently demonstrated the highest induction of gene expression. Most inter-lobe differences were attenuated at later time points (5 h). To improve reproducibility of the study of endotoxemia induced by i.p. LPS challenge, inclusion of appropriate methodological details regarding collection of hepatic tissue should be included when reporting scientific results in published manuscripts. SAGE Publications 2019-02-06 2019-02 /pmc/articles/PMC6784545/ /pubmed/30774009 http://dx.doi.org/10.1177/1753425918823900 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Nguyen, Leanna Sandoval, Jeryl De Dios, Robyn Yihdego, Elesa Zarate, Miguel Castro, Odalis McKenna, Sarah Wright, Clyde J The hepatic innate immune response is lobe-specific in a murine model endotoxemia |
title | The hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
title_full | The hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
title_fullStr | The hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
title_full_unstemmed | The hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
title_short | The hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
title_sort | hepatic innate immune response is lobe-specific in a murine model
endotoxemia |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784545/ https://www.ncbi.nlm.nih.gov/pubmed/30774009 http://dx.doi.org/10.1177/1753425918823900 |
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