Evidence map›Paper›PMID 30218099›Full record

ArticleScientific reports2018

Imaging of human cells exposed to an antifungal antibiotic amphotericin B reveals the mechanisms associated with the drug toxicity and cell defence.

Ewa Grela, Mateusz Piet, Rafal Luchowski, Wojciech Grudzinski, Roman Paduch, Wieslaw I Gruszecki

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.8field-weighted citation impact, top 3% of its field
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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Raman Study of PathogenicFrontiers in microbiology · 2022
    Article
  12. PeerJ · 2022
    Article
  13. Review
  14. Journal of fungi (Basel, Switzerland) · 2021
    Review
  15. Review
  16. In vitro activities ofCurrent medical mycology · 2020
    Article
  17. Article
  18. Review
  19. Review
  20. Article
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 at 2 institutions in 1 country.

Ewa GrelaDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Mateusz PietDepartment of Virology and Immunology, Institute of Microbiology and Biotechnology, Maria Curie-Skłodowska University, Lublin, Poland.
Rafal LuchowskiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Wojciech GrudzinskiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.ORCID 0000-0002-8825-1423
Roman PaduchDepartment of Virology and Immunology, Institute of Microbiology and Biotechnology, Maria Curie-Skłodowska University, Lublin, Poland.
Wieslaw I GruszeckiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland. wieslaw.gruszecki@umcs.pl.ORCID 0000-0002-8245-3913
Maria Curie-Skłodowska University · PLMedical University of Lublin · PL

Funding

Narodowe Centrum Nauki (National Science Centre) 2015/19/B/NZ7/02159
6 · The paper itself

Abstract

Amphotericin B is an antibiotic used in pharmacotherapy of life-threatening mycotic infections. Unfortunately, the applicability of this antibiotic is associated with highly toxic side effects. In order to understand molecular mechanisms underlying toxicity of amphotericin B to patients, two cell lines, human normal colon epithelial cells (CCD 841 CoTr) and human colon adenocarcinoma cells (HT-29) were cultured in the presence of the drug and imaged with the application of fluorescence lifetime imaging microscopy and Raman scattering microscopy. The results of the cell viability assays confirm high toxicity of amphotericin B towards human cells. The images recorded demonstrate effective binding of amphotericin B to biomembranes. Analysis of the images reveals the operation of a defence mechanism based upon the elimination of molecules of the drug from living cells via formation of small amphotericin B-containing lipid vesicles. The fact that exosomes formed are devoid of cholesterol, as concluded on the basis of the results of Raman analysis, suggests that sequestration of sterols from the lipid phase of biomembranes is not a sole mechanism responsible for the toxic side effects of amphotericin B. Alternatively, the results imply that molecules of the drug present directly within the hydrophobic membrane core disturb the lipid membrane structure and affect their biological functions.

Indexed as

Microscopy, FluorescenceAmphotericin BAnti-Bacterial AgentsAntifungal AgentsCell SurvivalHT29 CellsHumansSpectrum Analysis, RamanAmphotericin BAnti-Bacterial AgentsAntifungal Agents

Identifiers

PMID30218099
PMCPMC6138690
OpenAlexW2890319039

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.