The orphan nuclear receptor Nur77 regulates LKB1 localization and activates AMPK - PubMed (original) (raw)

. 2012 Nov;8(11):897-904.

doi: 10.1038/nchembio.1069. Epub 2012 Sep 16.

Yan Chen, Qian Zhang, Jia-jia Zhuang, Min Tian, Hang-zi Chen, Lian-ru Zhang, Hong-kui Zhang, Jian-ping He, Wei-jia Wang, Rong Wu, Yuan Wang, Chunfang Shi, Kai Yang, An-zhong Li, Yong-zhen Xin, Terytty Yang Li, James Y Yang, Zhong-hui Zheng, Chun-dong Yu, Sheng-Cai Lin, Chawnshang Chang, Pei-qiang Huang, Tianwei Lin, Qiao Wu

Affiliations

The orphan nuclear receptor Nur77 regulates LKB1 localization and activates AMPK

Yan-yan Zhan et al. Nat Chem Biol. 2012 Nov.

Abstract

Liver kinase B1 (LKB1) has important roles in governing energy homeostasis by regulating the activity of the energy sensor kinase AMP-activated protein kinase (AMPK). The regulation of LKB1 function, however, is still poorly understood. Here we demonstrate that the orphan nuclear receptor Nur77 binds and sequesters LKB1 in the nucleus, thereby attenuating AMPK activation. This Nur77 function is antagonized by the chemical compound ethyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate (TMPA), which interacts with Nur77 with high affinity and at specific sites. TMPA binding of Nur77 results in the release and shuttling of LKB1 to the cytoplasm to phosphorylate AMPKα. Moreover, TMPA effectively reduces blood glucose and alleviates insulin resistance in type II db/db and high-fat diet- and streptozotocin-induced diabetic mice but not in diabetic littermates with the Nur77 gene knocked out. This study attains a mechanistic understanding of the regulation of LKB1-AMPK axis and implicates Nur77 as a new and amenable target for the design and development of therapeutics to treat metabolic diseases.

PubMed Disclaimer

Comment in

Similar articles

Cited by

References

    1. Nat Struct Mol Biol. 2008 Aug;15(8):865-7 - PubMed
    1. Circulation. 2008 Feb 19;117(7):952-62 - PubMed
    1. J Appl Physiol (1985). 1997 Jan;82(1):219-25 - PubMed
    1. EMBO J. 2003 Oct 1;22(19):5102-14 - PubMed
    1. Mol Endocrinol. 2011 Oct;25(10):1773-85 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources