학술논문

HIF-independent role of prolyl hydroxylases in the cellular response to amino acids.
Document Type
Article
Source
Oncogene. 9/19/2013, Vol. 32 Issue 38, p4549-4556. 8p. 2 Black and White Photographs, 1 Diagram, 4 Graphs.
Subject
*HYDROXYLASES
*HYPOXIA-inducible factors
*DIOXYGENASES
*AMINO acid metabolism
*RAPAMYCIN
*TARGETED drug delivery
Language
ISSN
0950-9232
Abstract
Hypoxia-inducible factor (HIF) prolyl hydroxylases (PHDs) are α-ketoglutarate (αKG)-dependent dioxygenases that function as cellular oxygen sensors. However, PHD activity also depends on factors other than oxygen, especially αKG, a key metabolic compound closely linked to amino-acid metabolism. We examined the connection between amino-acid availability and PHD activity. We found that amino-acid starvation leads to αKG depletion and to PHD inactivation but not to HIF stabilization. Furthermore, pharmacologic or genetic inhibition of PHDs induced autophagy and prevented mammalian target of rapamycin complex 1 (mTORC1) activation by amino acids in a HIF-independent manner. Therefore, PHDs sense not only oxygen but also respond to amino acids, constituting a broad intracellular nutrient-sensing network. [ABSTRACT FROM AUTHOR]