Evidence map›Paper›PMID 34070594›Full record

ArticleInternational journal of molecular sciences2021

Self-Targeting of Carbon Dots into the Cell Nucleus: Diverse Mechanisms of Toxicity in NIH/3T3 and L929 Cells.

Markéta Havrdová, Iztok Urbančič, Kateřina Bartoň Tománková, Lukáš Malina, Janez Štrancar, Athanasios B Bourlinos

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
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  14. Review
  15. A Review of in vivo Toxicity of Quantum Dots in Animal Models.International journal of nanomedicine · 2023
    Review
  16. Carbon quantum dots in bioimaging and biomedicines.Frontiers in bioengineering and biotechnology · 2023
    Review
  17. Article
  18. Article
  19. Quantum Dots and Their Interaction with Biological Systems.International journal of molecular sciences · 2022
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Markéta HavrdováRegional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute, Palacký University, Křížkovského 511/8, 779 00 Olomouc, Czech Republic.
Iztok UrbančičLaboratory of Biophysics, Condensed Matter Physics Department, "Jozef Stefan" Institute, Jamova 39, 1000 Ljubljana, Slovenia.ORCID 0000-0003-3603-6585
Kateřina Bartoň TománkováDepartment of Medical Biophysics, Faculty of Medicine and Dentistry, Institute of Translation Medicine, Palacký University in Olomouc, Hněvotínská 3, 775 15 Olomouc, Czech Republic.ORCID 0000-0002-3249-4522
Lukáš MalinaDepartment of Medical Biophysics, Faculty of Medicine and Dentistry, Institute of Translation Medicine, Palacký University in Olomouc, Hněvotínská 3, 775 15 Olomouc, Czech Republic.ORCID 0000-0001-5734-5921
Janez ŠtrancarLaboratory of Biophysics, Condensed Matter Physics Department, "Jozef Stefan" Institute, Jamova 39, 1000 Ljubljana, Slovenia.
Athanasios B BourlinosPhysics Department, University of Ioannina, 45110 Ioannina, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is important to understand the nanomaterials intracellular trafficking and distribution and investigate their targeting into the nuclear area in the living cells. In our previous study, we firstly observed penetration of nonmodified positively charged carbon dots decorated with quaternary ammonium groups (QCDs) into the nucleus of mouse NIH/3T3 fibroblasts. Thus, in this work, we focused on deeper study of QCDs distribution inside two healthy mouse NIH/3T3 and L929 cell lines by fluorescence microspectroscopy and performed a comprehensive cytotoxic and DNA damage measurements. Real-time penetration of QCDs across the plasma cell membrane was recorded, concentration dependent uptake was determined and endocytic pathways were characterized. We found out that the QCDs concentration of 200 µg/mL is close to saturation and subsequently, NIH/3T3 had a different cell cycle profile, however, no significant changes in viability (not even in the case with QCDs in the nuclei) and DNA damage. In the case of L929, the presence of QCDs in the nucleus evoked a cellular death. Intranuclear environment of NIH/3T3 cells affected fluorescent properties of QCDs and evoked fluorescence blue shifts. Studying the intracellular interactions with CDs is essential for development of future applications such as DNA sensing, because CDs as DNA probes have not yet been developed.

Indexed as

CarbonQuantum DotsAnimalsCell CycleCell MembraneCell NucleusCell SurvivalFibroblastsMiceMicroscopy, FluorescenceNIH 3T3 CellsCarboncarbon dotscnucleuscytotoxicityfibroblastsfluorescence microspectroscopygenotoxicityL929NIH/3T3nucleolus

Identifiers

PMID34070594
PMCPMC8198156

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Registered trials

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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.