Lithium induces autophagy by inhibiting inositol monophosphatase
University of Cambridge · Addenbrooke's Hospital
Abstract
Macroautophagy is a key pathway for the clearance of aggregate-prone cytosolic proteins. Currently, the only suitable pharmacologic strategy for up-regulating autophagy in mammalian cells is to use rapamycin, which inhibits the mammalian target of rapamycin (mTOR), a negative regulator of autophagy. Here we describe a novel mTOR-independent pathway that regulates autophagy. We show that lithium induces autophagy, and thereby, enhances the clearance of autophagy substrates, like mutant huntingtin and alpha-synucleins. This effect is not mediated by glycogen synthase kinase 3beta inhibition. The autophagy-enhancing properties of lithium were mediated by inhibition of inositol monophosphatase and led to free…
Citation impact
- FWCI
- 13.09
- Percentile
- 100%
- References
- 40
Authors
8- SSSovan SarkarCorresponding
University of Cambridge, Addenbrooke's Hospital
- RAR. Andrés Floto
University of Cambridge, Addenbrooke's Hospital
- ZBZdenek Berger
University of Cambridge, Addenbrooke's Hospital
- SISara Imarisio
University of Cambridge, Addenbrooke's Hospital
- ACAxelle Cordenier
University of Cambridge, Addenbrooke's Hospital
Topics & keywords
- Autophagy
- PI3K/AKT/mTOR pathway
- Biology
- Inositol
- Cell biology
- ATG16L1
- BAG3
- Cytosol
- Good health and well-being