Bile acid receptor agonist GW4064 regulates PPARγ coactivator-1α expression through estrogen receptor-related receptor α

Shailendra Kumar Dhar Dwivedi, Nidhi Singh, Rashmi Kumari, Jay Sharan Mishra, Sarita Tripathi, Priyam Banerjee, Priyanka Shah, Vandana Kukshal, Abdul Malik Tyagi, Anil Nilkanth Gaikwad, Rajnish Kumar Chaturvedi, Durga Prasad Mishra, Arun Kumar Trivedi, Somali Sanyal, Naibedya Chattopadhyay, Ravishankar Ramachandran, Mohammad Imran Siddiqi, Arun Bandyopadhyay, Ashish Arora, Thomas LundåsenSayee Priyadarshini Anakk, David D. Moore, Sabyasachi Sanyal

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


Peroxisome proliferator-activated receptorγ coactivator-1α (PGC-1α) is induced in energy-starved conditions and is a key regulator of energy homeostasis. This makes PGC-1α an attractive therapeutic target for metabolic syndrome and diabetes. In our effort to identify new regulators of PGC-1α expression, we found that GW4064, a widely used synthetic agonist for the nuclear bile acid receptor [farnesoid X receptor (FXR)] strongly enhances PGC-1α promoter reporter activity, mRNA, and protein expression. This induction in PGC-1α concomitantly enhances mitochondrial mass and expression of several PGC-1α target genes involved in mitochondrial function. Using FXR-rich or FXR-nonexpressing cell lines and tissues, we found that this effect of GW4064 is not mediated directly by FXR but occurs via activation of estrogen receptor-related receptor α (ERRα). Cell-based, biochemical and biophysical assays indicate GW4064 as an agonist of ERR proteins. Interestingly, FXR disruption alters GW4064 induction of PGC-1α mRNA in a tissue-dependent manner. Using FXR-null [FXR knockout (FXRKO)] mice, we determined that GW4064 induction of PGC-1α expression is not affected in oxidative soleus muscles of FXRKO mice but is compromised in the FXRKO liver. Mechanistic studies to explain these differencesrevealed that FXR physically interacts with ERR and protects them from repression by the atypical corepressor, small heterodimer partner in liver. Together, this interplay between ERRα-FXRPGC-1α and small heterodimer partner offers new insights into the biological functions of ERRα and FXR, thus providing a knowledge base for therapeutics in energy balance-related pathophysiology.

Original languageEnglish (US)
Pages (from-to)922-932
Number of pages11
JournalMolecular Endocrinology
Issue number6
StatePublished - Jun 2011
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology


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