Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure

Patients with acute-on-chronic liver failure (ACLF) are at risk of developing acute hepatic decompensation and organ failures with an unraveled complex mechanism. An altered immune response toward insults in cirrhotic compared with healthy livers may contribute to the ACLF development. Therefore, we...

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Main Author: Suriguga S.
Other Authors: Mahidol University
Format: Article
Published: 2023
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/83655
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spelling th-mahidol.836552023-06-18T23:46:08Z Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure Suriguga S. Mahidol University Biochemistry, Genetics and Molecular Biology Patients with acute-on-chronic liver failure (ACLF) are at risk of developing acute hepatic decompensation and organ failures with an unraveled complex mechanism. An altered immune response toward insults in cirrhotic compared with healthy livers may contribute to the ACLF development. Therefore, we aim to investigate the differences in inflammatory responses between cirrhotic and healthy livers using human precision-cut liver slices (PCLSs) upon the lipopolysaccharide (LPS) challenge. PCLSs prepared from livers of patients with cirrhosis or healthy donors of liver transplantation were incubated ex vivo with or without LPS for up to 48 h. Viability test, qRT-PCR, and multiplex cytokine assay were performed. Regulation of the LPS receptors during incubation or with LPS challenge differed between healthy versus cirrhotic PCLSs. LPS upregulated TLR-2 in healthy PCLSs solely (P < 0.01). Culturing for 48 h induced a stronger inflammatory response in the cirrhotic than healthy PCLS. Upon LPS stimulation, cirrhotic PCLSs secreted more proinflammatory cytokines (IL-8, IL-6, TNF-α, eotaxin, and VEGF) significantly and less antiinflammatory cytokine (IL-1ra) than those of healthy. In summary, cirrhotic PCLSs released more proinflammatory and less antiinflammatory cytokines after LPS stimuli than healthy, leading to dysregulated inflammatory response. These events could possibly resemble the liver immune response in ACLF. 2023-06-18T16:46:08Z 2023-06-18T16:46:08Z 2022-08-01 Article American Journal of Physiology - Gastrointestinal and Liver Physiology Vol.323 No.2 (2022) , G114-G125 10.1152/ajpgi.00243.2021 15221547 01931857 35727919 2-s2.0-85134854493 https://repository.li.mahidol.ac.th/handle/123456789/83655 SCOPUS
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
spellingShingle Biochemistry, Genetics and Molecular Biology
Suriguga S.
Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
description Patients with acute-on-chronic liver failure (ACLF) are at risk of developing acute hepatic decompensation and organ failures with an unraveled complex mechanism. An altered immune response toward insults in cirrhotic compared with healthy livers may contribute to the ACLF development. Therefore, we aim to investigate the differences in inflammatory responses between cirrhotic and healthy livers using human precision-cut liver slices (PCLSs) upon the lipopolysaccharide (LPS) challenge. PCLSs prepared from livers of patients with cirrhosis or healthy donors of liver transplantation were incubated ex vivo with or without LPS for up to 48 h. Viability test, qRT-PCR, and multiplex cytokine assay were performed. Regulation of the LPS receptors during incubation or with LPS challenge differed between healthy versus cirrhotic PCLSs. LPS upregulated TLR-2 in healthy PCLSs solely (P < 0.01). Culturing for 48 h induced a stronger inflammatory response in the cirrhotic than healthy PCLS. Upon LPS stimulation, cirrhotic PCLSs secreted more proinflammatory cytokines (IL-8, IL-6, TNF-α, eotaxin, and VEGF) significantly and less antiinflammatory cytokine (IL-1ra) than those of healthy. In summary, cirrhotic PCLSs released more proinflammatory and less antiinflammatory cytokines after LPS stimuli than healthy, leading to dysregulated inflammatory response. These events could possibly resemble the liver immune response in ACLF.
author2 Mahidol University
author_facet Mahidol University
Suriguga S.
format Article
author Suriguga S.
author_sort Suriguga S.
title Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
title_short Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
title_full Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
title_fullStr Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
title_full_unstemmed Distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: Possible implications for acute-on-chronic liver failure
title_sort distinct responses between healthy and cirrhotic human livers upon lipopolysaccharide challenge: possible implications for acute-on-chronic liver failure
publishDate 2023
url https://repository.li.mahidol.ac.th/handle/123456789/83655
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