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NF-кB increases LPS-mediated procalcitonin production in human hepatocytes

For years, procalcitonin (PCT) has been employed as a diagnostic biomarker for the severity of sepsis and septic shock, as well as for guiding the application of antibiotics. However, the molecular/cellular basis for the regulation of PCT production is not fully understood. In this study, we identif...

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Autores principales: Bai, Yongfeng, Lu, Jun, Cheng, Ying, Zhang, Feng, Fan, Xueyu, Weng, Yuanyuan, Zhu, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995812/
https://www.ncbi.nlm.nih.gov/pubmed/29891911
http://dx.doi.org/10.1038/s41598-018-27302-7
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author Bai, Yongfeng
Lu, Jun
Cheng, Ying
Zhang, Feng
Fan, Xueyu
Weng, Yuanyuan
Zhu, Jin
author_facet Bai, Yongfeng
Lu, Jun
Cheng, Ying
Zhang, Feng
Fan, Xueyu
Weng, Yuanyuan
Zhu, Jin
author_sort Bai, Yongfeng
collection PubMed
description For years, procalcitonin (PCT) has been employed as a diagnostic biomarker for the severity of sepsis and septic shock, as well as for guiding the application of antibiotics. However, the molecular/cellular basis for the regulation of PCT production is not fully understood. In this study, we identified the signalling pathway by which the expression of PCT was induced by lipopolysaccharide in human hepatocytes at the mRNA and protein levels. This expression was dependent on nuclear transcription factor κB (NF-κB), as indicated by a NF-κB binding site (nt −53 to −44) found in the PCT promoter region. We also showed that microRNA-513b (miR-513b) was also able to bind to the 3′-untranslated region (UTR) of the PCT promoter sequence. Meanwhile, the activation of NF-κB down-regulated the expression of miR-513b. In conclusion, we suggest that NF-κB is capable of enhancing the expression of PCT by either directly activating the transcription of the PCT gene or indirectly modulating the expression of its regulatory component, miR-513b. Our results indicate a molecular mechanism responsible for the regulation of PCT production.
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spelling pubmed-59958122018-06-21 NF-кB increases LPS-mediated procalcitonin production in human hepatocytes Bai, Yongfeng Lu, Jun Cheng, Ying Zhang, Feng Fan, Xueyu Weng, Yuanyuan Zhu, Jin Sci Rep Article For years, procalcitonin (PCT) has been employed as a diagnostic biomarker for the severity of sepsis and septic shock, as well as for guiding the application of antibiotics. However, the molecular/cellular basis for the regulation of PCT production is not fully understood. In this study, we identified the signalling pathway by which the expression of PCT was induced by lipopolysaccharide in human hepatocytes at the mRNA and protein levels. This expression was dependent on nuclear transcription factor κB (NF-κB), as indicated by a NF-κB binding site (nt −53 to −44) found in the PCT promoter region. We also showed that microRNA-513b (miR-513b) was also able to bind to the 3′-untranslated region (UTR) of the PCT promoter sequence. Meanwhile, the activation of NF-κB down-regulated the expression of miR-513b. In conclusion, we suggest that NF-κB is capable of enhancing the expression of PCT by either directly activating the transcription of the PCT gene or indirectly modulating the expression of its regulatory component, miR-513b. Our results indicate a molecular mechanism responsible for the regulation of PCT production. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995812/ /pubmed/29891911 http://dx.doi.org/10.1038/s41598-018-27302-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bai, Yongfeng
Lu, Jun
Cheng, Ying
Zhang, Feng
Fan, Xueyu
Weng, Yuanyuan
Zhu, Jin
NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title_full NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title_fullStr NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title_full_unstemmed NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title_short NF-кB increases LPS-mediated procalcitonin production in human hepatocytes
title_sort nf-кb increases lps-mediated procalcitonin production in human hepatocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995812/
https://www.ncbi.nlm.nih.gov/pubmed/29891911
http://dx.doi.org/10.1038/s41598-018-27302-7
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