Modulation of Autophagy by a Small Molecule Inverse Agonist of ERR? Is Neuroprotective.

ABSTRACT: Mechanistic insights into aggrephagy, a selective basal autophagy process to clear misfolded protein aggregates, are lacking. Here, we report and describe the role of Estrogen Related Receptor ? (ERR?, HUGO Gene Nomenclature ESRRA), new molecular player of aggrephagy, in keeping autophagy flux in check by inhibiting autophagosome formation. A screen for small molecule modulators for aggrephagy identified ERR? inverse agonist XCT 790, that cleared ?-synuclein aggregates in an autophagy dependent, but mammalian target of rapamycin (MTOR) independent manner. XCT 790 modulates autophagosome formation in an ERR? dependent manner as validated by siRNA mediated knockdown and over expression approaches. We show that, in a basal state, ERR? is localized on to the autophagosomes and upon autophagy induction by XCT 790, this localization is lost and is accompanied with an increase in autophagosome biogenesis. In a preclinical mouse model of Parkinson's disease (PD), XCT 790 exerted neuroprotective effects in the dopaminergic neurons of nigra by inducing autophagy to clear toxic protein aggregates and, in addition, ameliorated motor co-ordination deficits. Using a chemical biology approach, we unrevealed the role of ERR? in regulating autophagy and can be therapeutic target for neurodegeneration.

SUBMITTER: Suresh SN 

PROVIDER: S-EPMC5900053 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature