Real-Time Visualization of Lysosome Destruction Using a Photosensitive Toluidine Blue Nanogel.

TitleReal-Time Visualization of Lysosome Destruction Using a Photosensitive Toluidine Blue Nanogel.
Publication TypeJournal Article
Year of Publication2018
AuthorsZhang W, Tung C-H
JournalChemistry
Volume24
Issue9
Pagination2089-2093
Date Published2018 Feb 09
ISSN1521-3765
KeywordsCell Line, Tumor, Flow Cytometry, Humans, Hyaluronic Acid, Light, Lysosomes, Microscopy, Electron, Transmission, Microscopy, Fluorescence, Nanogels, Polyethylene Glycols, Polyethyleneimine, Reactive Oxygen Species, Spectrophotometry, Tolonium Chloride
Abstract

Breaking the lysosome helps its sequestered payloads access their molecular targets in cells and thus enhances the intracellular drug delivery. Current strategies for lysosomal escape involve direct physical interactions with the lipid membrane. These interactions pose a systemic toxicity and uncontrolled membrane rupture risk. Here, we report a light-detonated lysosome disruption using a hyaluronan (HA) nanogel packed with toludine blue (TB). The HA/TB nanogel is concentrated within the lysosomes. The applied light assists TB in generating reactive oxygen species and destroying the lysosome in situ, both in cells and isolated lysosomes. Real time fluorescent tracking reveals that quenched TB fluorescence recovers along with lysosome explosion, relocates to the nucleus, and is presented as a fluorescent sparkling in cells. This HA/TB, composed of all clinically approved materials, represents a biocompatible and facile strategy to "bomb" lysosomes in a spatiotemporally controlled fashion.

DOI10.1002/chem.201705697
Alternate JournalChemistry
PubMed ID29314346
PubMed Central IDPMC6309271
Grant ListR01 GM094880 / GM / NIGMS NIH HHS / United States
Related Institute: 
Molecular Imaging Innovations Institute (MI3)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065