Depletion of p18/LAMTOR1 promotes cell survival via activation of p27(kip1)-dependent autophagy under starvation

作者：Zada Sahib; Noh Hae Sook; Baek Seon Mi; Ha Ji Hye; Hahm Jong Ryeal; Kim Deok Ryong^*

来源：Cell Biology International, 2015, 39(11): 1242-1250.

DOI：10.1002/cbin.10497

• autophagy
• MAPK
• mTORC1
• p18
• LAMTOR1
• p27(kip1)
• starvation-induced cell death

The MAPK and mTOR signal pathways in endosomes or lysosomes play a crucial role in cell survival and death. They are also closely associated with autophagy, a catabolic process highly regulated under various cellular stress or nutrient deprivation. Recently we have isolated a protein, named p18/LAMTOR1, that specifically regulates the ERK or mTOR pathway in lysosomes. p18/LAMTOR1 also interacts with p27(kip1). Here we examined how p18/LAMTOR1 plays a role in autophagy under nutrient deprivation. The p18(+/+) MEF cells were more susceptible to cell death under starvation or in the presence of AICAR in comparison with p18(-/-) MEF cells. Cleavage of caspase-3 was increased in p18(+/+) MEF cells under starvation, and phosphorylation at the threonine 198 of p27(kip1) was highly elevated in starved p18(-/-) MEF cells. Furthermore, LC3-II formation and other autophagy-associated proteins were largely increased in p18-deficient cells, and suppression of p27(kip1) expression in p18(-/-) MEF cells mitigated starvation-induced cell death. These data suggest that ablation of p18/LAMTOR1 suppresses starvation-induced cell death by stimulating autophagy through modulation of p27(kip1) activity.

• 出版日期2015-11