Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles

被引:54
作者
Qiu, Kangqiang [1 ,2 ]
Du, Yang [2 ,3 ]
Liu, Jiyan [3 ]
Guan, Jun-Lin [2 ]
Chao, Hui [1 ]
Diao, Jiajie [2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] Univ Cincinnati, Dept Canc Biol, Coll Med, Cincinnati, OH 45267 USA
[3] Sichuan Univ, West China Hosp, West China Med Sch, Dept Biotherapy,Canc Ctr,State Key Lab Biotherapy, Chengdu 610041, Peoples R China
基金
美国国家科学基金会;
关键词
super-resolution imaging; structured illumination microscopy; lysosomes; mitophagy; long-term labelling; LONG-TERM; AUTOPHAGY; MITOCHONDRIA; FUSION; PROBE; ORGANELLES; TRACKING; DELIVERY; CELLS;
D O I
10.7150/thno.42134
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Because lysosomes play critical roles in multiple cellular functions and are associated with many diseases, studying them at the subcellular level could elucidate their functionality and support the discovery of therapeutic drugs for treating those diseases. The commonly used dyes for super-resolution imaging of lysosomes are the commercial molecular LysoTrackers. But the tolerance to changes in the lysosomal microenvironment and to lysosomal membrane permeabilization (LMP) and the photostability of the LysoTrackers are worrisome. The purpose of our study was to evaluate the feasibility of performing a fluorescent gold nanoprobe for super-resolution observation of lysosomal dynamics in living cells and compare it to the commercial LysoTrackers. Methods: The nanoprobe CyS@Au NP contained three parts: a bio-inert gold core, a biocompatible polyethylene glycol spacer, and a fluorophore cyanine 5. Structured illumination microscopy (SIM) was employed to capture the fluorescence of Cy5@Au NPs in cells. The tolerance assays to changes in the lysosomal microenvironment and to LMP, the photobleaching assay, and the long-term lysosomes labelling assay of Cy5@Au NPs were compared with commercial LysoTrackers. The super-resolution observation of lysosomal dynamics with Cy5@Au NPs was performed. Results: Cy5@Au NPs can light up lysosomes specifically under SIM. Compared with commercial lysosomal molecular probes, Cy5@Au NPs exhibited stronger tolerance in lysosomes during various treatments, and changes in the lysosomal microenvironment and LMP did not cause CyS@Au NPs to lose track of their targets. CyS@Au NPs demonstrated an excellent anti-photobleaching ability, and a long-term labelling assay revealed that they could label lysosomes more than 3 d. Biological events of lysosomes such as the kiss-and-run process, fusion, fission, and mitophagy were recorded with the fluorescent Cy5@Au NPs under SIM. Conclusions: The nanoprobe Cy5@Au NP was successfully used as a lysosomal probe for the super-resolution observation in living cells and found to overcome the limitations of commercial LysoTrackers. Our results thus confirm that nanoparticles can be useful tools for subcellular super-resolution imaging and highlight new avenues for using nanoparticles in biology.
引用
收藏
页码:6072 / 6081
页数:10
相关论文
共 72 条
[1]   Whole-Cell Scale Dynamic Organization of Lysosomes Revealed by Spatial Statistical Analysis [J].
Ba, Qinle ;
Raghavan, Guruprasad ;
Kiselyov, Kirill ;
Yang, Ge .
CELL REPORTS, 2018, 23 (12) :3591-3606
[2]   High-Discrimination Factor Nanosensor Based on Tetrahedral DNA Nanostructures and Gold Nanoparticles for Detection of MiRNA-21 in Live Cells [J].
Bai, Shulian ;
Xu, Bangtian ;
Guo, Yongcan ;
Qiu, Juhui ;
Yu, Wen ;
Xie, Guoming .
THERANOSTICS, 2018, 8 (09) :2424-2434
[3]   Lysosomes as dynamic regulators of cell and organismal homeostasis [J].
Ballabio, Andrea ;
Bonifacino, Juan S. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2020, 21 (02) :101-118
[4]   Endocytic delivery to lysosomes mediated by concurrent fusion and kissing events in living cells [J].
Bright, NA ;
Gratian, MJ ;
Luzio, JP .
CURRENT BIOLOGY, 2005, 15 (04) :360-365
[5]   CHOLESTEROL SENSING Lysosomal cholesterol activates mTORC1 via an SLC38A9-Niemann-Pick C1 signaling complex [J].
Castellano, Brian M. ;
Thelen, Ashley M. ;
Moldavski, Ofer ;
Feltes, McKenna ;
van der Welle, Reini E. N. ;
Mydock-McGrane, Laurel ;
Jiang, Xuntian ;
Van Eijkeren, Robert J. ;
Davis, Oliver B. ;
Louie, Sharon M. ;
Perera, Rushika M. ;
Covey, Douglas F. ;
Nomura, Daniel K. ;
Ory, Daniel S. ;
Zoncu, Roberto .
SCIENCE, 2017, 355 (6331) :1306-1311
[6]   Mitochondrial Dynamics and Its Involvement in Disease [J].
Chan, David C. .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 15, 2020, 2020, 15 :235-259
[7]   Quantitative analysis of interactive behavior of mitochondria and lysosomes using structured illumination microscopy [J].
Chen, Qixin ;
Shao, Xintian ;
Hao, Mingang ;
Fang, Hongbao ;
Guan, Ruilin ;
Tian, Zhiqi ;
Li, Miaoling ;
Wang, Chenran ;
Ji, Liangnian ;
Chao, Hui ;
Guan, Jun-Lin ;
Diao, Jiajie .
BIOMATERIALS, 2020, 250
[8]   Nanoscale monitoring of mitochondria and lysosome interactions for drug screening and discovery [J].
Chen, Qixin ;
Shao, Xintian ;
Tian, Zhiqi ;
Chen, Yang ;
Mondal, Payel ;
Liu, Fei ;
Wang, Fengshan ;
Ling, Peixue ;
He, Weijiang ;
Zhang, Kai ;
Guo, Zijian ;
Diao, Jiajie .
NANO RESEARCH, 2019, 12 (05) :1009-1015
[9]   Super-Resolution Tracking of Mitochondrial Dynamics with An Iridium(III) Luminophore [J].
Chen, Qixin ;
Jin, Chengzhi ;
Shao, Xintian ;
Guan, Ruilin ;
Tian, Zhiqi ;
Wang, Chenran ;
Liu, Fei ;
Ling, Peixue ;
Guan, Jun-Lin ;
Ji, Liangnian ;
Wang, Fengshan ;
Chao, Hui ;
Diao, Jiajie .
SMALL, 2018, 14 (41)
[10]   One-Step Synthesis of Ultrasmall and Ultrabright Organosilica Nanodots with 100% Photoluminescence Quantum Yield: Long-Term Lysosome Imaging in Living, Fixed, and Permeabilized Cells [J].
Chen, Xiaokai ;
Zhang, Xiaodong ;
Xia, Liu-Yuan ;
Wang, Hong-Yin ;
Chen, Zhan ;
Wu, Fu-Gen .
NANO LETTERS, 2018, 18 (02) :1159-1167