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消化不良之外:基于溶酶体的信号传导在人类疾病中的新作用

Beyond indigestion: emerging roles for lysosome-based signaling in human disease.

作者信息

Ferguson Shawn M

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, CT, 06510, United States; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510, United States.

出版信息

Curr Opin Cell Biol. 2015 Aug;35:59-68. doi: 10.1016/j.ceb.2015.04.014. Epub 2015 May 15.

DOI:10.1016/j.ceb.2015.04.014
PMID:25950843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4529762/
Abstract

Lysosomes are becoming increasingly recognized as a hub that integrates diverse signals in order to control multiple aspects of cell physiology. This is illustrated by the discovery of a growing number of lysosome-localized proteins that respond to changes in growth factor and nutrient availability to regulate mTORC1 signaling as well as the identification of MiT/TFE transcription factors (MITF, TFEB and TFE3) as proteins that shuttle between lysosomes and the nucleus to elicit a transcriptional response to ongoing changes in lysosome status. These findings have been paralleled by advances in human genetics that connect mutations in genes involved in lysosomal signaling to a broad range of human illnesses ranging from cancer to neurological disease. This review summarizes these new discoveries at the interface between lysosome cell biology and human disease.

摘要

溶酶体日益被视为一个整合多种信号以控制细胞生理学多个方面的枢纽。越来越多定位于溶酶体的蛋白质被发现,它们可响应生长因子和营养可用性的变化来调节mTORC1信号传导,以及MiT/TFE转录因子(MITF、TFEB和TFE3)被鉴定为在溶酶体和细胞核之间穿梭以引发对溶酶体状态持续变化的转录反应的蛋白质,这些都说明了这一点。人类遗传学的进展也与此相呼应,这些进展将参与溶酶体信号传导的基因突变与从癌症到神经疾病等广泛的人类疾病联系起来。本综述总结了溶酶体细胞生物学与人类疾病交叉领域的这些新发现。

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Lysosomal TBK1 Responds to Amino Acid Availability to Relieve Rab7-Dependent mTORC1 Inhibition.溶酶体中的TBK1对氨基酸可用性做出反应,以解除Rab7依赖性的mTORC1抑制。
bioRxiv. 2023 Dec 17:2023.12.16.571979. doi: 10.1101/2023.12.16.571979.
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LRRK2 suppresses lysosome degradative activity in macrophages and microglia through MiT-TFE transcription factor inhibition.

本文引用的文献

1
Nutrient-sensing mechanisms across evolution.进化过程中的营养感知机制。
Cell. 2015 Mar 26;161(1):67-83. doi: 10.1016/j.cell.2015.02.041.
2
Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy.MTOR 中的脑体细胞突变导致 II 型局灶性皮质发育不良,进而引发难治性癫痫。
Nat Med. 2015 Apr;21(4):395-400. doi: 10.1038/nm.3824. Epub 2015 Mar 23.
3
Lysosomal calcium signalling regulates autophagy through calcineurin and ​TFEB.溶酶体钙信号通过钙调神经磷酸酶和 TFEB 调节自噬。
LRRK2 通过 MiT-TFE 转录因子抑制抑制巨噬细胞和小神经胶质细胞中的溶酶体降解活性。
Proc Natl Acad Sci U S A. 2023 Aug;120(31):e2303789120. doi: 10.1073/pnas.2303789120. Epub 2023 Jul 24.
4
Phosphorylated S6K1 and 4E-BP1 play different roles in constitutively active Rheb-mediated retinal ganglion cell survival and axon regeneration after optic nerve injury.磷酸化的S6K1和4E-BP1在组成型活性Rheb介导的视神经损伤后视网膜神经节细胞存活和轴突再生中发挥不同作用。
Neural Regen Res. 2023 Nov;18(11):2526-2534. doi: 10.4103/1673-5374.371372.
5
A two-tiered system for selective receptor and transporter protein degradation.双层体系用于选择性受体和转运蛋白降解。
PLoS Genet. 2022 Oct 10;18(10):e1010446. doi: 10.1371/journal.pgen.1010446. eCollection 2022 Oct.
6
JIP3 links lysosome transport to regulation of multiple components of the axonal cytoskeleton.JIP3 将溶酶体运输与轴突细胞骨架的多个成分的调节联系起来。
Commun Biol. 2022 Jan 10;5(1):5. doi: 10.1038/s42003-021-02945-x.
7
Prodigiosin inhibits cholangiocarcinoma cell proliferation and induces apoptosis via suppressing SNAREs-dependent autophagy.灵菌红素通过抑制SNAREs依赖性自噬来抑制胆管癌细胞增殖并诱导其凋亡。
Cancer Cell Int. 2021 Dec 9;21(1):658. doi: 10.1186/s12935-021-02355-3.
8
Perspectives on Organelle Interaction, Protein Dysregulation, and Cancer Disease.细胞器相互作用、蛋白质失调与癌症疾病的观点
Front Cell Dev Biol. 2021 Feb 25;9:613336. doi: 10.3389/fcell.2021.613336. eCollection 2021.
9
Crosstalks between inflammasome and autophagy in cancer.炎症小体与自噬在癌症中的相互作用。
J Hematol Oncol. 2020 Jul 23;13(1):100. doi: 10.1186/s13045-020-00936-9.
10
CDK4/6 regulate lysosome biogenesis through TFEB/TFE3.CDK4/6 通过 TFEB/TFE3 调节溶酶体生物发生。
J Cell Biol. 2020 Aug 3;219(8). doi: 10.1083/jcb.201911036.
Nat Cell Biol. 2015 Mar;17(3):288-99. doi: 10.1038/ncb3114.
4
MITF drives endolysosomal biogenesis and potentiates Wnt signaling in melanoma cells.小眼畸形相关转录因子(MITF)驱动内溶酶体生物合成并增强黑色素瘤细胞中的Wnt信号传导。
Proc Natl Acad Sci U S A. 2015 Feb 3;112(5):E420-9. doi: 10.1073/pnas.1424576112. Epub 2015 Jan 20.
5
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.雷帕霉素哺乳动物靶点通路突变导致半侧巨脑畸形和局灶性皮质发育不良。
Ann Neurol. 2015 Apr;77(4):720-5. doi: 10.1002/ana.24357. Epub 2015 Feb 26.
6
Nutrient-sensing mechanisms and pathways.营养感知机制与途径。
Nature. 2015 Jan 15;517(7534):302-10. doi: 10.1038/nature14190.
7
Metabolism. Differential regulation of mTORC1 by leucine and glutamine.代谢。亮氨酸和谷氨酰胺对mTORC1的差异调节。
Science. 2015 Jan 9;347(6218):194-8. doi: 10.1126/science.1259472. Epub 2015 Jan 7.
8
Metabolism. Lysosomal amino acid transporter SLC38A9 signals arginine sufficiency to mTORC1.代谢。溶酶体氨基酸转运蛋白SLC38A9向mTORC1发出精氨酸充足的信号。
Science. 2015 Jan 9;347(6218):188-94. doi: 10.1126/science.1257132. Epub 2015 Jan 7.
9
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Nature. 2015 Mar 26;519(7544):477-81. doi: 10.1038/nature14107. Epub 2015 Jan 7.
10
mTOR signaling in cellular and organismal energetics.细胞和机体能量代谢中的mTOR信号传导
Curr Opin Cell Biol. 2015 Apr;33:55-66. doi: 10.1016/j.ceb.2014.12.001. Epub 2014 Dec 31.