Wu Xiaochun, Zhao Lingling, Chen Zhi, Ji Xin, Qiao Xianfeng, Jin Yaping, Liu Wei
Key Laboratory of Animal Biotechnology, the Ministry of Agriculture, College of Veterinary Medicine, Northwest Agriculture & Forest University, Yangling, Shaanxi, China.
PLoS One. 2016 Jun 9;11(6):e0157100. doi: 10.1371/journal.pone.0157100. eCollection 2016.
The intracellular amino acid pool within lysosome is a signal that stimulates the nutrient-sensing mTORC1 signalling pathway. The signal transduction cascade has garnered much attention, but little is known about the sequestration of the signalling molecules within the lysosome. Using human HEK293 cells as a model, we found that suppression of the BHD syndrome gene FLCN reduced the leucine level in lysosome, which correlated with decreased mTORC1 activity. Both consequences could be reversed by supplementation with high levels of leucine, but not other tested amino acids. Conversely, overexpressed FLCN could sequester lysosomal leucine and stimulate mTORC1 in an amino acid limitation environment. These results identify a novel function of FLCN: it controls mTORC1 by modulating the leucine signal in lysosome. Furthermore, we provided evidence that FLCN exerted this role by inhibiting the accumulation of the amino acid transporter PAT1 on the lysosome surface, thereby maintaining the signal level within the organelle.
溶酶体内的细胞内氨基酸池是一种刺激营养感应mTORC1信号通路的信号。该信号转导级联反应备受关注,但对于溶酶体内信号分子的隔离却知之甚少。以人HEK293细胞为模型,我们发现BHD综合征基因FLCN的抑制降低了溶酶体内的亮氨酸水平,这与mTORC1活性降低相关。通过补充高水平的亮氨酸而非其他测试氨基酸,这两种结果均可逆转。相反,过表达的FLCN可隔离溶酶体亮氨酸并在氨基酸限制环境中刺激mTORC1。这些结果确定了FLCN的一种新功能:它通过调节溶酶体内的亮氨酸信号来控制mTORC1。此外,我们提供的证据表明,FLCN通过抑制氨基酸转运蛋白PAT1在溶酶体表面的积累来发挥这一作用,从而维持细胞器内的信号水平。