Scientific Publications

Small molecules enhance autophagy and reduce toxicity in Huntington's disease models.

Publication TypeJournal Article
AuthorsSarkar, S., Perlstein EO, Imarisio S., Pineau S., Cordenier A., Maglathlin RL, Webster JA, Lewis TA, O'Kane CJ, Schreiber SL, and Rubinsztein DC
AbstractThe target of rapamycin proteins regulate various cellular processes including autophagy, which may play a protective role in certain neurodegenerative and infectious diseases. Here we show that a primary small-molecule screen in yeast yields novel small-molecule modulators of mammalian autophagy. We first identified new small-molecule enhancers (SMER) and inhibitors (SMIR) of the cytostatic effects of rapamycin in Saccharomyces cerevisiae. Three SMERs induced autophagy independently of rapamycin in mammalian cells, enhancing the clearance of autophagy substrates such as mutant huntingtin and A53T alpha-synuclein, which are associated with Huntington's disease and familial Parkinson's disease, respectively. These SMERs, which seem to act either independently or downstream of the target of rapamycin, attenuated mutant huntingtin-fragment toxicity in Huntington's disease cell and Drosophila melanogaster models, which suggests therapeutic potential. We also screened structural analogs of these SMERs and identified additional candidate drugs that enhanced autophagy substrate clearance. Thus, we have demonstrated proof of principle for a new approach for discovery of small-molecule modulators of mammalian autophagy.
Year of Publication2007
JournalNature chemical biology
Volume3
Issue6
Pages331-8
Date Published (YYYY/MM/DD)2007/06/01
ISSN Number1552-4450
DOI10.1038/nchembio883
PubMedhttp://www.ncbi.nlm.nih.gov/pubmed/17486044?dopt=Abstract