Cargando…

Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles

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-resoluti...

Descripción completa

Detalles Bibliográficos
Autores principales: Qiu, Kangqiang, Du, Yang, Liu, Jiyan, Guan, Jun-Lin, Chao, Hui, Diao, Jiajie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254985/
https://www.ncbi.nlm.nih.gov/pubmed/32483439
http://dx.doi.org/10.7150/thno.42134
_version_ 1783539642877870080
author Qiu, Kangqiang
Du, Yang
Liu, Jiyan
Guan, Jun-Lin
Chao, Hui
Diao, Jiajie
author_facet Qiu, Kangqiang
Du, Yang
Liu, Jiyan
Guan, Jun-Lin
Chao, Hui
Diao, Jiajie
author_sort Qiu, Kangqiang
collection PubMed
description 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 Cy5@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 Cy5@Au NPs to lose track of their targets. Cy5@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.
format Online
Article
Text
id pubmed-7254985
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-72549852020-05-31 Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles Qiu, Kangqiang Du, Yang Liu, Jiyan Guan, Jun-Lin Chao, Hui Diao, Jiajie Theranostics Research Paper 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 Cy5@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 Cy5@Au NPs to lose track of their targets. Cy5@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. Ivyspring International Publisher 2020-05-15 /pmc/articles/PMC7254985/ /pubmed/32483439 http://dx.doi.org/10.7150/thno.42134 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Qiu, Kangqiang
Du, Yang
Liu, Jiyan
Guan, Jun-Lin
Chao, Hui
Diao, Jiajie
Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title_full Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title_fullStr Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title_full_unstemmed Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title_short Super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
title_sort super-resolution observation of lysosomal dynamics with fluorescent gold nanoparticles
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254985/
https://www.ncbi.nlm.nih.gov/pubmed/32483439
http://dx.doi.org/10.7150/thno.42134
work_keys_str_mv AT qiukangqiang superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles
AT duyang superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles
AT liujiyan superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles
AT guanjunlin superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles
AT chaohui superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles
AT diaojiajie superresolutionobservationoflysosomaldynamicswithfluorescentgoldnanoparticles