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Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction
Glucagon promotes hepatic gluconeogenesis and maintains whole-body glucose levels during fasting. The regulatory factors that are involved in fasting glucagon response are not well understood. Here we report a role of p52, a key activator of the noncanonical nuclear factor-kappaB signaling, in hepat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754499/ https://www.ncbi.nlm.nih.gov/pubmed/31541100 http://dx.doi.org/10.1038/s41467-019-12351-x |
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author | Zhang, Wen-Song Pan, An Zhang, Xu Ying, Ang Ma, Gaoxiang Liu, Bao-Lin Qi, Lian-Wen Liu, Qun Li, Ping |
author_facet | Zhang, Wen-Song Pan, An Zhang, Xu Ying, Ang Ma, Gaoxiang Liu, Bao-Lin Qi, Lian-Wen Liu, Qun Li, Ping |
author_sort | Zhang, Wen-Song |
collection | PubMed |
description | Glucagon promotes hepatic gluconeogenesis and maintains whole-body glucose levels during fasting. The regulatory factors that are involved in fasting glucagon response are not well understood. Here we report a role of p52, a key activator of the noncanonical nuclear factor-kappaB signaling, in hepatic glucagon response. We show that p52 is activated in livers of HFD-fed and glucagon-challenged mice. Knockdown of p52 lowers glucagon-stimulated hyperglycemia, while p52 overexpression augments glucagon response. Mechanistically, p52 binds to phosphodiesterase 4B promoter to inhibit its transcription and promotes cAMP accumulation, thus augmenting the glucagon response through cAMP/PKA signaling. The anti-diabetic drug metformin and ginsenoside Rb1 lower blood glucose at least in part by inhibiting p52 activation. Our findings reveal that p52 mediates glucagon-triggered hepatic gluconeogenesis and suggests that pharmacological intervention to prevent p52 processing is a potential therapeutic strategy for diabetes. |
format | Online Article Text |
id | pubmed-6754499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67544992019-09-23 Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction Zhang, Wen-Song Pan, An Zhang, Xu Ying, Ang Ma, Gaoxiang Liu, Bao-Lin Qi, Lian-Wen Liu, Qun Li, Ping Nat Commun Article Glucagon promotes hepatic gluconeogenesis and maintains whole-body glucose levels during fasting. The regulatory factors that are involved in fasting glucagon response are not well understood. Here we report a role of p52, a key activator of the noncanonical nuclear factor-kappaB signaling, in hepatic glucagon response. We show that p52 is activated in livers of HFD-fed and glucagon-challenged mice. Knockdown of p52 lowers glucagon-stimulated hyperglycemia, while p52 overexpression augments glucagon response. Mechanistically, p52 binds to phosphodiesterase 4B promoter to inhibit its transcription and promotes cAMP accumulation, thus augmenting the glucagon response through cAMP/PKA signaling. The anti-diabetic drug metformin and ginsenoside Rb1 lower blood glucose at least in part by inhibiting p52 activation. Our findings reveal that p52 mediates glucagon-triggered hepatic gluconeogenesis and suggests that pharmacological intervention to prevent p52 processing is a potential therapeutic strategy for diabetes. Nature Publishing Group UK 2019-09-20 /pmc/articles/PMC6754499/ /pubmed/31541100 http://dx.doi.org/10.1038/s41467-019-12351-x Text en © The Author(s) 2019 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 Zhang, Wen-Song Pan, An Zhang, Xu Ying, Ang Ma, Gaoxiang Liu, Bao-Lin Qi, Lian-Wen Liu, Qun Li, Ping Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title | Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title_full | Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title_fullStr | Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title_full_unstemmed | Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title_short | Inactivation of NF-κB2 (p52) restrains hepatic glucagon response via preserving PDE4B induction |
title_sort | inactivation of nf-κb2 (p52) restrains hepatic glucagon response via preserving pde4b induction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754499/ https://www.ncbi.nlm.nih.gov/pubmed/31541100 http://dx.doi.org/10.1038/s41467-019-12351-x |
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