• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用新型基因编码生物传感器对细胞系和原代神经元培养物中的溶酶体内 pH 进行实时成像。

Live imaging of intra-lysosome pH in cell lines and primary neuronal culture using a novel genetically encoded biosensor.

机构信息

Department of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.

Experimental Imaging Center, San Raffaele Scientific Institute, Milan, Italy.

出版信息

Autophagy. 2021 Jun;17(6):1500-1518. doi: 10.1080/15548627.2020.1771858. Epub 2020 Jun 9.

DOI:10.1080/15548627.2020.1771858
PMID:32515674
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8205096/
Abstract

Disorders of lysosomal physiology have increasingly been found to underlie the pathology of a rapidly growing cast of neurodevelopmental disorders and sporadic diseases of aging. One cardinal aspect of lysosomal (dys)function is lysosomal acidification in which defects trigger lysosomal stress signaling and defects in proteolytic capacity. We have developed a genetically encoded ratiometric probe to measure lysosomal pH coupled with a purification tag to efficiently purify lysosomes for both proteomic and evaluation of their function. Using our probe, we showed that lysosomal pH is remarkably stable over a period of days in a variety of cell types. Additionally, this probe can be used to determine that lysosomal stress signaling TFEB is uncoupled from gross changes in lysosomal pH. Finally, we demonstrated that while overexpression of ARL8B GTPase causes striking alkalinization of peripheral lysosomes in HEK293 T cells, peripheral lysosomes are no less acidic than juxtanuclear lysosomes in our cell lines. ARL8B: ADP ribosylation factor like GTPase 8B; ATP: adenosine triphosphate; ATP5F1B/ATPB: ATP synthase F1 subunit beta; ATP6V1A: ATPase H+ transporting V1 subunit A; Baf: bafilomycin A; BLOC-1: biogenesis of lysosome-related organelles complex 1; BSA: bovine serum albumin; Cos7: African green monkey kidney fibroblast-like cell line; CQ: chloroquine; CTSB: cathepsin B; CYCS: cytochrome c, somatic; DAPI: 4',6-diamidino -2- phenylindole; DIC: differential interference contrast; DIV: days ; DMEM: Dulbecco's modified Eagle's medium;‎ E8: embryonic day 8; EEA1: early endosome antigen 1; EGTA: ethylene glycol-bis(β-aminoethyl ether)-N,N,N',N'-tetraacetic acid; ER: endoplasmic reticulum; FBS: fetal bovine serum; FITC: fluorescein isothiocyanate; GABARAPL2: GABA type A receptor associated protein like 2; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GOLGA2/GM130: golgin A2; GTP: guanosine triphosphate; HEK293T: human embryonic kidney 293 cells, that expresses a mutant version of the SV40 large T antigen; HeLa: Henrietta Lacks-derived cell; HEPES: 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid; HRP: horseradish peroxidase; IGF2R/ciM6PR: insulin like growth factor 2 receptor; LAMP1/2: lysosomal associated membrane protein 1/2; LMAN2/VIP36: lectin, mannose binding 2; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MTORC1: mechanistic target of rapamycin kinase complex 1; PCR: polymerase chain reaction; PDL: poly-d-lysine; : promotor from human phosphoglycerate kinase 1; PIKFYVE: phosphoinositide kinase, FYVE-type zinc finger containing; PPT1/CLN1: palmitoyl-protein thioesterase 1; RPS6KB1/p70: ribosomal protein S6 kinase B1; STAT3: signal transducer and activator of transcription 3; TAX1BP1: Tax1 binding protein 1; TFEB: transcription factor EB; TGN: trans-Golgi network; TGOLN2/TGN46: trans-Golgi network protein 2; TIRF: total internal reflection fluorescence; TMEM106B: transmembrane protein 106B; TOR: target of rapamycin; TRPM2: transient receptor potential cation channel subfamily M member 2; V-ATPase: vacuolar-type proton-translocating ATPase; VPS35: VPS35 retromer complex component.

摘要

溶酶体生理学的紊乱越来越被认为是神经发育障碍和散发性衰老疾病的快速发展的病理基础。溶酶体(功能)障碍的一个主要方面是溶酶体酸化,其中缺陷触发溶酶体应激信号和蛋白水解能力缺陷。我们开发了一种遗传编码的比率探针来测量与纯化标签耦合的溶酶体 pH,以有效地纯化溶酶体进行蛋白质组学和功能评估。使用我们的探针,我们表明在各种细胞类型中,溶酶体 pH 在几天的时间内非常稳定。此外,该探针可用于确定溶酶体应激信号 TFEB 与溶酶体 pH 的总体变化无关。最后,我们证明,虽然 ARL8B GTPase 的过表达导致 HEK293T 细胞中外周溶酶体的明显碱化,但在外周溶酶体中,它们并不比我们的细胞系中的核周溶酶体更酸性。ARL8B:类似于 GTPase 的 ADP 核糖基化因子 8B;ATP:三磷酸腺苷;ATP5F1B/ATPB:ATP 合酶 F1 亚基β;ATP6V1A:ATP 酶 H+转运 V1 亚基 A;Baf:巴弗霉素 A;BLOC-1:溶酶体相关细胞器生物发生复合物 1;BSA:牛血清白蛋白;Cos7:非洲绿猴肾成纤维样细胞系;CQ:氯喹;CTSB:组织蛋白酶 B;CYCS:细胞色素 c,体细胞;DAPI:4',6-二脒基-2-苯吲哚;DIC:微分干涉对比;DIV:天;DMEM:杜尔贝科改良 Eagle 培养基;E8:胚胎第 8 天;EEA1:早期内体抗原 1;EGTA:乙二醇双(β-氨基乙基醚)-N,N,N',N'-四乙酸;内质网;FBS:胎牛血清;FITC:荧光素异硫氰酸酯;GABARAPL2:GABA 型 A 受体相关蛋白样 2;GAPDH:甘油醛-3-磷酸脱氢酶;GOLGA2/GM130:高尔基体 A2;GTP:鸟苷三磷酸;HEK293T:表达 SV40 大 T 抗原突变体的人胚肾 293 细胞;HeLa:Henrietta Lacks 细胞;HEPES:4-(2-羟乙基)-1-哌嗪乙磺酸;HRP:辣根过氧化物酶;IGF2R/ciM6PR:胰岛素样生长因子 2 受体;LAMP1/2:溶酶体相关膜蛋白 1/2;LMAN2/VIP36:凝集素,甘露糖结合 2;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;MTORC1:雷帕霉素激酶复合物 1 的机械靶标;PCR:聚合酶链反应;PDL:多聚-d-赖氨酸;:人磷酸甘油酸激酶 1 的启动子;PIKFYVE:磷酸肌醇激酶,含有 FYVE 型锌指;PPT1/CLN1:棕榈酰蛋白硫酯酶 1;RPS6KB1/p70:核糖体蛋白 S6 激酶 B1;STAT3:信号转导和转录激活因子 3;TAX1BP1:Tax1 结合蛋白 1;TFEB:转录因子 EB;TGN:高尔基网络;TGOLN2/TGN46:高尔基网络蛋白 2;TIRF:全内反射荧光;TMEM106B:跨膜蛋白 106B;TOR:雷帕霉素靶蛋白;TRPM2:瞬时受体电位阳离子通道亚家族 M 成员 2;V-ATPase:液泡型质子转运 ATP 酶;VPS35:VPS35 逆行复合成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/bbd4464059ad/KAUP_A_1771858_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/205face9d0fb/KAUP_A_1771858_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/c35d6a53d339/KAUP_A_1771858_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/86d2437c83fb/KAUP_A_1771858_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/b0fa95c4b5b6/KAUP_A_1771858_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/fa195efb6655/KAUP_A_1771858_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/bbd4464059ad/KAUP_A_1771858_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/205face9d0fb/KAUP_A_1771858_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/c35d6a53d339/KAUP_A_1771858_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/86d2437c83fb/KAUP_A_1771858_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/b0fa95c4b5b6/KAUP_A_1771858_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/fa195efb6655/KAUP_A_1771858_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7700/8205096/bbd4464059ad/KAUP_A_1771858_F0006_C.jpg

相似文献

1
Live imaging of intra-lysosome pH in cell lines and primary neuronal culture using a novel genetically encoded biosensor.利用新型基因编码生物传感器对细胞系和原代神经元培养物中的溶酶体内 pH 进行实时成像。
Autophagy. 2021 Jun;17(6):1500-1518. doi: 10.1080/15548627.2020.1771858. Epub 2020 Jun 9.
2
Mitochondrial respiratory chain deficiency inhibits lysosomal hydrolysis.线粒体呼吸链缺陷抑制溶酶体水解。
Autophagy. 2019 Sep;15(9):1572-1591. doi: 10.1080/15548627.2019.1586256. Epub 2019 Mar 27.
3
A family of PIKFYVE inhibitors with therapeutic potential against autophagy-dependent cancer cells disrupt multiple events in lysosome homeostasis.一组具有治疗潜力的 PIKFYVE 抑制剂可针对自噬依赖性癌细胞,破坏溶酶体动态平衡中的多个事件。
Autophagy. 2019 Oct;15(10):1694-1718. doi: 10.1080/15548627.2019.1586257. Epub 2019 Mar 8.
4
ATM loss disrupts the autophagy-lysosomal pathway.ATM 缺失破坏自噬溶酶体途径。
Autophagy. 2021 Aug;17(8):1998-2010. doi: 10.1080/15548627.2020.1805860. Epub 2020 Aug 14.
5
Phosphorylation of EIF2S1 (eukaryotic translation initiation factor 2 subunit alpha) is indispensable for nuclear translocation of TFEB and TFE3 during ER stress.EIF2S1(真核翻译起始因子 2 亚基 alpha)的磷酸化对于 ER 应激过程中 TFEB 和 TFE3 的核易位是必不可少的。
Autophagy. 2023 Jul;19(7):2111-2142. doi: 10.1080/15548627.2023.2173900. Epub 2023 Feb 9.
6
Impaired TFEB-mediated lysosomal biogenesis promotes the development of pancreatitis in mice and is associated with human pancreatitis.TFEB 介导的溶酶体生物发生受损促进了小鼠胰腺炎的发展,并与人类胰腺炎有关。
Autophagy. 2019 Nov;15(11):1954-1969. doi: 10.1080/15548627.2019.1596486. Epub 2019 Mar 30.
7
PSEN2 (presenilin 2) mutants linked to familial Alzheimer disease impair autophagy by altering Ca homeostasis.PSEN2(早老素 2)突变与家族性阿尔茨海默病相关,通过改变钙稳态来损害自噬。
Autophagy. 2019 Dec;15(12):2044-2062. doi: 10.1080/15548627.2019.1596489. Epub 2019 Mar 27.
8
GNS561, a clinical-stage PPT1 inhibitor, is efficient against hepatocellular carcinoma modulation of lysosomal functions.GNS561,一种临床阶段的 PPT1 抑制剂,对肝癌有效,能调节溶酶体功能。
Autophagy. 2022 Mar;18(3):678-694. doi: 10.1080/15548627.2021.1988357. Epub 2021 Nov 5.
9
Ischemia-induced upregulation of autophagy preludes dysfunctional lysosomal storage and associated synaptic impairments in neurons.缺血诱导的自噬上调先于神经元中功能失调的溶酶体储存和相关的突触损伤。
Autophagy. 2021 Jun;17(6):1519-1542. doi: 10.1080/15548627.2020.1840796. Epub 2020 Nov 12.
10
Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration.海藻糖通过溶酶体介导的 TFEB 激活诱导运动神经元退变模型中的自噬。
Autophagy. 2019 Apr;15(4):631-651. doi: 10.1080/15548627.2018.1535292. Epub 2018 Nov 5.

引用本文的文献

1
Breaking the cellular delivery bottleneck: recent developments in direct cytosolic delivery of biologics.突破细胞递送瓶颈:生物制剂直接胞质递送的最新进展
RSC Pharm. 2025 Jul 2. doi: 10.1039/d5pm00129c.
2
Modular Calcium-Responsive and CD9-Targeted Phospholipase System Enhancing Endosomal Escape for DNA Delivery.模块化钙响应和CD9靶向磷脂酶系统增强用于DNA递送的内体逃逸
Adv Sci (Weinh). 2025 Apr;12(15):e2410815. doi: 10.1002/advs.202410815. Epub 2025 Feb 25.
3
αAsarone alleviates neuronal injury by facilitating autophagy via miR-499-5p/PDCD4/ATG5 signaling pathway in ischemia stroke.

本文引用的文献

1
Inhibition of the glutamine transporter SNAT1 confers neuroprotection in mice by modulating the mTOR-autophagy system.抑制谷氨酰胺转运体 SNAT1 通过调节 mTOR-自噬系统在小鼠中发挥神经保护作用。
Commun Biol. 2019 Sep 18;2:346. doi: 10.1038/s42003-019-0582-4. eCollection 2019.
2
Mitochondrial respiratory chain deficiency inhibits lysosomal hydrolysis.线粒体呼吸链缺陷抑制溶酶体水解。
Autophagy. 2019 Sep;15(9):1572-1591. doi: 10.1080/15548627.2019.1586256. Epub 2019 Mar 27.
3
Reciprocal Regulation of V-ATPase and Glycolytic Pathway Elements in Health and Disease.
α-细辛醚通过miR-499-5p/PDCD4/ATG5信号通路促进自噬来减轻缺血性脑卒中的神经元损伤。
Front Pharmacol. 2025 Jan 23;16:1504683. doi: 10.3389/fphar.2025.1504683. eCollection 2025.
4
Quantitative profiling pH heterogeneity of acidic endolysosomal compartments using fluorescence lifetime imaging microscopy.使用荧光寿命成像显微镜对酸性内溶酶体区室的pH异质性进行定量分析。
Mol Biol Cell. 2025 Mar 1;36(3):br8. doi: 10.1091/mbc.E23-06-0220. Epub 2025 Jan 29.
5
Identification of crucial pathways and genes linked to endoplasmic reticulum stress in PCOS through combined bioinformatic analysis.通过联合生物信息学分析鉴定与多囊卵巢综合征内质网应激相关的关键通路和基因
Front Mol Biosci. 2025 Jan 9;11:1504015. doi: 10.3389/fmolb.2024.1504015. eCollection 2024.
6
RpH-ILV: Probe for lysosomal pH and acute LLOMe-induced membrane permeabilization in cell lines and .RpH-ILV:用于细胞系中溶酶体pH值及急性碘乙酰胺诱导的膜通透性检测的探针
Sci Adv. 2025 Jan 3;11(1):eadr7325. doi: 10.1126/sciadv.adr7325.
7
Molecular Spies in Action: Genetically Encoded Fluorescent Biosensors Light up Cellular Signals.分子间谍大显身手:基因编码荧光生物传感器点亮细胞信号。
Chem Rev. 2024 Nov 27;124(22):12573-12660. doi: 10.1021/acs.chemrev.4c00293. Epub 2024 Nov 13.
8
STIM1 functions as a proton sensor to coordinate cytosolic pH with store-operated calcium entry.基质相互作用分子1(STIM1)作为一种质子传感器,通过钙库操纵性钙内流来协调胞质pH值。
J Biol Chem. 2024 Dec;300(12):107924. doi: 10.1016/j.jbc.2024.107924. Epub 2024 Oct 23.
9
Mechanisms of autophagy-lysosome dysfunction in neurodegenerative diseases.神经退行性疾病中自噬-溶酶体功能障碍的机制。
Nat Rev Mol Cell Biol. 2024 Nov;25(11):926-946. doi: 10.1038/s41580-024-00757-5. Epub 2024 Aug 6.
10
Schisandra chinensis inhibits the entry of BoHV-1 by blocking PI3K-Akt pathway and enhances the m6A methylation of gD to inhibit the entry of progeny virus.五味子通过阻断PI3K-Akt信号通路抑制牛疱疹病毒1型(BoHV-1)的侵入,并增强gD的m6A甲基化以抑制子代病毒的侵入。
Front Microbiol. 2024 Jul 22;15:1444414. doi: 10.3389/fmicb.2024.1444414. eCollection 2024.
健康与疾病中V-ATP酶与糖酵解途径元件的相互调节
Front Physiol. 2019 Feb 15;10:127. doi: 10.3389/fphys.2019.00127. eCollection 2019.
4
Ubiquilins regulate autophagic flux through mTOR signalling and lysosomal acidification.泛素结合蛋白通过调控 mTOR 信号和溶酶体酸化来调节自噬通量。
Nat Cell Biol. 2019 Mar;21(3):384-396. doi: 10.1038/s41556-019-0281-x. Epub 2019 Feb 25.
5
A systematic approach to identify recycling endocytic cargo depending on the GARP complex.一种基于 GARP 复合物有系统地识别再循环内吞货物的方法。
Elife. 2019 Jan 29;8:e42837. doi: 10.7554/eLife.42837.
6
The lysosome as a cellular centre for signalling, metabolism and quality control.溶酶体作为细胞信号转导、代谢和质量控制的中心。
Nat Cell Biol. 2019 Feb;21(2):133-142. doi: 10.1038/s41556-018-0244-7. Epub 2019 Jan 2.
7
Lysosomotropic drugs activate TFEB via lysosomal membrane fluidization and consequent inhibition of mTORC1 activity.溶酶体靶向药物通过溶酶体膜流化激活 TFEB,并由此抑制 mTORC1 活性。
Cell Death Dis. 2018 Dec 13;9(12):1191. doi: 10.1038/s41419-018-1227-0.
8
Apilimod, a candidate anticancer therapeutic, arrests not only PtdIns(3,5)P2 but also PtdIns5P synthesis by PIKfyve and induces bafilomycin A1-reversible aberrant endomembrane dilation.阿泊利莫德,一种候选抗癌治疗药物,不仅能抑制 PIKfyve 介导的 PtdIns(3,5)P2 的合成,还能抑制 PtdIns5P 的合成,并诱导巴弗洛霉素 A1 逆转的异常内膜扩张。
PLoS One. 2018 Sep 21;13(9):e0204532. doi: 10.1371/journal.pone.0204532. eCollection 2018.
9
STAT3 associates with vacuolar H-ATPase and regulates cytosolic and lysosomal pH.STAT3 与液泡型 H+-ATP 酶结合并调节细胞质和溶酶体的 pH 值。
Cell Res. 2018 Oct;28(10):996-1012. doi: 10.1038/s41422-018-0080-0. Epub 2018 Aug 20.
10
The small G protein Arl8 contributes to lysosomal function and long-range axonal transport in .小G蛋白Arl8有助于溶酶体功能和……中的长距离轴突运输。 (原文句末不完整)
Biol Open. 2018 Sep 5;7(9):bio035964. doi: 10.1242/bio.035964.