| Literature DB >> 24953654 |
Eva Maria Gleixner1, Guillaume Canaud2, Tobias Hermle3, Maria Clara Guida1, Oliver Kretz4, Martin Helmstädter3, Tobias B Huber5, Stefan Eimer4, Fabiola Terzi2, Matias Simons6.
Abstract
mTOR kinase is a master growth regulator that can be stimulated by multiple signals, including amino acids and the lysosomal small GTPase Rheb. Recent studies have proposed an important role for the V-ATPase in the sensing of amino acids in the lysosomal lumen. Using the Drosophila wing as a model epithelium, we show here that the V-ATPase is required for Rheb-dependent epithelial growth. We further uncover a positive feedback loop for the control of apical protein uptake that depends on V-ATPase/mTOR signaling. This feedback loop includes Rheb-dependent transcriptional regulation of the multiligand receptor Megalin, which itself is required for Rheb-induced endocytosis. In addition, we provide evidence that long-term mTOR inhibition with rapamycin in mice causes reduction of Megalin levels and proteinuria in the proximal tubular epithelium of the kidney. Thus, our findings unravel a homeostatic mechanism that allows epithelial cells to promote protein uptake under normal conditions and to prevent uptake in lysosomal stress conditions.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24953654 DOI: 10.1016/j.celrep.2014.05.035
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423