LAPTM4b recruits the LAT1-4F2hc Leu transporter to lysosomes and promotes mTORC1 activation

被引:157
|
作者
Milkereit, Ruth [1 ]
Persaud, Avinash [1 ]
Vanoaica, Liviu [2 ]
Guetg, Adriano [2 ]
Verrey, Francois [2 ]
Rotin, Daniela [1 ]
机构
[1] Univ Toronto, Hosp Sick Children, Dept Biochem, Cell Biol Program, Toronto, ON M5G 0A4, Canada
[2] Univ Zurich, Inst Physiol, Ctr Integrat Human Physiol ZIHP & NCCR Kidney, CH-8057 Zurich, Switzerland
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
AMINO-ACIDS; HEPATOCELLULAR-CARCINOMA; GROWTH; MECHANISMS; RESISTANCE; TARGETS; CANCER;
D O I
10.1038/ncomms8250
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mammalian target of rapamycin 1 (mTORC1), a master regulator of cellular growth, is activated downstream of growth factors, energy signalling and intracellular essential amino acids (EAAs) such as Leu. mTORC1 activation occurs at the lysosomal membrane, and involves V-ATPase stimulation by intra-lysosomal EAA (inside-out activation), leading to activation of the Ragulator, RagA/B-GTP and mTORC1 via Rheb-GTP. How Leu enters the lysosomes is unknown. Here we identified the lysosomal protein LAPTM4b as a binding partner for the Leu transporter, LAT1-4F2hc (SLC7A5-SLAC3A2). We show that LAPTM4b recruits LAT1-4F2hc to lysosomes, leading to uptake of Leu into lysosomes, and is required for mTORC1 activation via V-ATPase following EAA or Leu stimulation. These results demonstrate a functional Leu transporter at the lysosome, and help explain the inside-out lysosomal activation of mTORC1 by Leu/EAA.
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页数:9
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