Evidence map›Paper›PMID 29107993›Full record

ArticlePloS one2017

Nanoencapsulated capsaicin changes migration behavior and morphology of madin darby canine kidney cell monolayers.

Mathias Kaiser, Luisa Pohl, Steffi Ketelhut, Lena Kastl, Christian Gorzelanny, Martin Götte, Jürgen Schnekenburger, Francisco M Goycoolea, Björn Kemper

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Machine Learning with Optical Phase Signatures for Phenotypic Profiling of Cell Lines.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2019
    Article
  6. Article
  7. 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

9 authors at 3 institutions in 2 countries.

Mathias KaiserInstitute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster, Schlossgarten 3, Münster, Germany.
Luisa PohlBiomedical Technology Center of the Medical Faculty, Westfälische Wilhelms-Universität Münster, Mendelstraße 17, Münster, Germany.
Steffi KetelhutBiomedical Technology Center of the Medical Faculty, Westfälische Wilhelms-Universität Münster, Mendelstraße 17, Münster, Germany.
Lena KastlBiomedical Technology Center of the Medical Faculty, Westfälische Wilhelms-Universität Münster, Mendelstraße 17, Münster, Germany.
Christian GorzelannyExperimental Dermatology, Department of Dermatology, Medical Faculty Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, Mannheim, Germany.
Martin GötteDepartment of Gynecology and Obstetrics, Westfälische Wilhelms-Universität Münster, Albert-Schweitzer-Campus 1, Münster, Germany.
Jürgen SchnekenburgerBiomedical Technology Center of the Medical Faculty, Westfälische Wilhelms-Universität Münster, Mendelstraße 17, Münster, Germany.
Francisco M GoycooleaInstitute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster, Schlossgarten 3, Münster, Germany.
Björn KemperBiomedical Technology Center of the Medical Faculty, Westfälische Wilhelms-Universität Münster, Mendelstraße 17, Münster, Germany.ORCID http://orcid.org/0000-0003-3693-9397
University of Münster · DEHeidelberg University · DEUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed a drug delivery nanosystem based on chitosan and capsaicin. Both substances have a wide range of biological activities. We investigated the nanosystem's influence on migration and morphology of Madin Darby canine kidney (MDCK-C7) epithelial cells in comparison to the capsaicin-free nanoformulation, free capsaicin, and control cells. For minimally-invasive quantification of cell migration, we applied label-free digital holographic microscopy (DHM) and single-cell tracking. Moreover, quantitative DHM phase images were used as novel stain-free assay to quantify the temporal course of global cellular morphology changes in confluent cell layers. Cytoskeleton alterations and tight junction protein redistributions were complementary analyzed by fluorescence microscopy. Calcium influx measurements were conducted to characterize the influence of the nanoformulations and capsaicin on ion channel activities. We found that both, capsaicin-loaded and unloaded chitosan nanocapsules, and also free capsaicin, have a significant impact on directed cell migration and cellular motility. Increase of velocity and directionality of cell migration correlates with changes in the cell layer surface roughness, tight junction integrity and cytoskeleton alterations. Calcium influx into cells occurred only after nanoformulation treatment but not upon addition of free capsaicin. Our results pave the way for further studies on the biological significance of these findings and potential biomedical applications, e.g. as drug and gene carriers.

Indexed as

NanocapsulesAnimalsCalciumCapsaicinCell MovementDogsMadin Darby Canine Kidney CellsMicroscopy, FluorescenceCalciumCapsaicinNanocapsules

Identifiers

PMID29107993
PMCPMC5673207
OpenAlexW2767420540

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.