Hesketh Geoffrey G, Wartosch Lena, Davis Luther J, Bright Nicholas A, Luzio J Paul
Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, M5G 1X5, Canada.
Department of Clinical Biochemistry and Cambridge Institute for Medical Research, School of Clinical Medicine, Wellcome Trust/MRC Building, University of Cambridge, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0XY, UK.
Prog Mol Subcell Biol. 2018;57:151-180. doi: 10.1007/978-3-319-96704-2_6.
In addition to being the terminal degradative compartment of the cell's endocytic and autophagic pathways, the lysosome is a multifunctional signalling hub integrating the cell's response to nutrient status and growth factor/hormone signalling. The cytosolic surface of the limiting membrane of the lysosome is the site of activation of the multiprotein complex mammalian target of rapamycin complex 1 (mTORC1), which phosphorylates numerous cell growth-related substrates, including transcription factor EB (TFEB). Under conditions in which mTORC1 is inhibited including starvation, TFEB becomes dephosphorylated and translocates to the nucleus where it functions as a master regulator of lysosome biogenesis. The signalling role of lysosomes is not limited to this pathway. They act as an intracellular Ca store, which can release Ca into the cytosol for both local effects on membrane fusion and pleiotropic effects within the cell. The relationship and crosstalk between the lysosomal and endoplasmic reticulum (ER) Ca stores play a role in shaping intracellular Ca signalling. Lysosomes also perform other signalling functions, which are discussed. Current views of the lysosomal compartment recognize its dynamic nature. It includes endolysosomes, autolysosome and storage lysosomes that are constantly engaged in fusion/fission events and lysosome regeneration. How signalling is affected by individual lysosomal organelles being at different stages of these processes and/or at different sites within the cell is poorly understood, but is discussed.
除了作为细胞内吞和自噬途径的终末降解区室外,溶酶体还是一个多功能信号枢纽,整合细胞对营养状态以及生长因子/激素信号的反应。溶酶体限制膜的胞质表面是雷帕霉素复合物1(mTORC1)多蛋白复合物激活的位点,mTORC1可磷酸化众多与细胞生长相关的底物,包括转录因子EB(TFEB)。在包括饥饿在内的mTORC1受到抑制的条件下,TFEB去磷酸化并转位至细胞核,在细胞核中它作为溶酶体生物发生的主要调节因子发挥作用。溶酶体的信号作用并不局限于这一途径。它们作为细胞内钙库,可将钙释放到胞质溶胶中,对膜融合产生局部影响,并在细胞内产生多效性作用。溶酶体与内质网(ER)钙库之间的关系和相互作用在塑造细胞内钙信号方面发挥作用。溶酶体还执行其他信号功能,本文将对此进行讨论。目前对溶酶体区室的看法认识到其动态性质。它包括内溶酶体、自噬溶酶体和储存溶酶体,它们不断参与融合/裂变事件以及溶酶体再生。目前对这些过程不同阶段的单个溶酶体细胞器和/或细胞内不同位点如何影响信号传导了解甚少,但本文将对此进行讨论。