Evidence map›Paper›PMID 23429995›Full record

ArticleInternational journal of nanomedicine2013

Intracellular distribution of nontargeted quantum dots after natural uptake and microinjection.

Leona Damalakiene, Vitalijus Karabanovas, Saulius Bagdonas, Mindaugas Valius, Ricardas Rotomskis

Abstract read
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Article in International journal of nanomedicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Review
  2. NIR fluorescence imaging and treatment for cancer immunotherapy.Journal for immunotherapy of cancer · 2022
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  6. Review
  7. Review
  8. Imaging techniques in nanomedical research.European journal of histochemistry : EJH · 2020
    Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Leona DamalakieneBiophotonics Group, Laser Research Center, Faculty of Physics, Vilnius University, Vilnius, Lithuania.
Vitalijus Karabanovas
Saulius Bagdonas
Mindaugas Valius
Ricardas Rotomskis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of this study was to elucidate the mechanism of natural uptake of nonfunctionalized quantum dots in comparison with microinjected quantum dots by focusing on their time-dependent accumulation and intracellular localization in different cell lines.

methodsThe accumulation dynamics of nontargeted CdSe/ZnS carboxyl-coated quantum dots (emission peak 625 nm) was analyzed in NIH3T3, MCF-7, and HepG2 cells by applying the methods of confocal and steady-state fluorescence spectroscopy. Intracellular colocalization of the quantum dots was investigated by staining with Lysotracker(®).

resultsThe uptake of quantum dots into cells was dramatically reduced at a low temperature (4 °C), indicating that the process is energy-dependent. The uptake kinetics and imaging of intracellular localization of quantum dots revealed three accumulation stages of carboxyl-coated quantum dots at 37 °C, ie, a plateau stage, growth stage, and a saturation stage, which comprised four morphological phases: adherence to the cell membrane; formation of granulated clusters spread throughout the cytoplasm; localization of granulated clusters in the perinuclear region; and formation of multivesicular body-like structures and their redistribution in the cytoplasm. Diverse quantum dots containing intracellular vesicles in the range of approximately 0.5-8 μm in diameter were observed in the cytoplasm, but none were found in the nucleus. Vesicles containing quantum dots formed multivesicular body-like structures in NIH3T3 cells after 24 hours of incubation, which were Lysotracker-negative in serum-free medium and Lysotracker-positive in complete medium. The microinjected quantum dots remained uniformly distributed in the cytosol for at least 24 hours.

conclusionNatural uptake of quantum dots in cells occurs through three accumulation stages via a mechanism requiring energy. The sharp contrast of the intracellular distribution after microinjection of quantum dots in comparison with incubation as well as the limited transfer of quantum dots from vesicles into the cytosol and vice versa support the endocytotic origin of the natural uptake of quantum dots. Quantum dots with proteins adsorbed from the culture medium had a different fate in the final stage of accumulation from that of the protein-free quantum dots, implying different internalization pathways.

Indexed as

Quantum DotsAnimalsCell Line, TumorEndocytosisGreen Fluorescent ProteinsHep G2 CellsHumansIntracellular SpaceMiceMicroinjectionsMicroscopy, ConfocalNIH 3T3 CellsGreen Fluorescent Proteinscarboxylendocytosisgreen fluorescent proteininternalizationlysosomemultivesicular body-like structurespathwayprotein coronaring-like vesiclessaturation

Identifiers

PMID23429995
PMCPMC3575178

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.