mTOR regulation of autophagy

Chang Hwa Jung(University of Minnesota), Seung‐Hyun Ro(University of Minnesota), Jing Cao(University of Minnesota), Neil Otto(University of Minnesota), Do‐Hyung Kim(University of Minnesota)
FEBS Letters
January 18, 2010
Cited by 2,088

Abstract

Nutrient starvation induces autophagy in eukaryotic cells through inhibition of TOR (target of rapamycin), an evolutionarily-conserved protein kinase. TOR, as a central regulator of cell growth, plays a key role at the interface of the pathways that coordinately regulate the balance between cell growth and autophagy in response to nutritional status, growth factor and stress signals. Although TOR has been known as a key regulator of autophagy for more than a decade, the underlying regulatory mechanisms have not been clearly understood. This review discusses the recent advances in understanding of the mechanism by which TOR regulates autophagy with focus on mammalian TOR (mTOR) and its regulation of the autophagy machinery.


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