Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Wen-Song, Pan, An, Zhang, Xu, Ying, Ang, Ma, Gaoxiang, Liu, Bao-Lin, Qi, Lian-Wen, Liu, Qun, Li, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783453085703602176
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
work_keys_str_mv AT zhangwensong inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT panan inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT zhangxu inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT yingang inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT magaoxiang inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT liubaolin inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT qilianwen inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT liuqun inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction
AT liping inactivationofnfkb2p52restrainshepaticglucagonresponseviapreservingpde4binduction