Nutrient regulation of mTORC1 at a glance.
Kendall J CondonDavid M SabatiniPublished in: Journal of cell science (2019)
The mechanistic target of rapamycin (mTOR) signaling pathway coordinates environmental and intracellular cues to control eukaryotic cell growth. As a pivot point between anabolic and catabolic processes, mTOR complex 1 (mTORC1) signaling has established roles in regulating metabolism, translation and autophagy. Hyperactivity of the mTOR pathway is associated with numerous human diseases, including diabetes, cancer and epilepsy. Pharmacological inhibition of the mTOR pathway can extend lifespan in a variety of model organisms. Given its broad control of essential cellular processes and clear relevance to human health, there is extensive interest in elucidating how upstream inputs regulate mTORC1 activation. In this Cell Science at a Glance article and accompanying poster, we summarize our understanding of how extracellular and intracellular signals feed into the mTOR pathway, how the lysosome acts as an mTOR signaling hub, and how downstream signaling controls autophagy and lysosome biogenesis.
Keyphrases
- cell proliferation
- signaling pathway
- human health
- risk assessment
- oxidative stress
- cell death
- endothelial cells
- type diabetes
- public health
- cardiovascular disease
- endoplasmic reticulum stress
- climate change
- squamous cell carcinoma
- living cells
- reactive oxygen species
- pi k akt
- adipose tissue
- metabolic syndrome
- skeletal muscle
- fluorescent probe
- induced apoptosis
- young adults
- induced pluripotent stem cells
- mesenchymal stem cells
- gram negative
- childhood cancer