Evidence map›Paper›PMID 32702063›Full record

ArticlePloS one2020

Measurement and visualization of cell membrane surface charge in fixed cultured cells related with cell morphology.

Masaru Nishino, Ibu Matsuzaki, Fidele Y Musangile, Yuichi Takahashi, Yoshifumi Iwahashi, Kenji Warigaya, Yuichi Kinoshita, Fumiyoshi Kojima, Shin-Ichi Murata

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.1field-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

38 citing papers in PubMed, 79 citations in OpenAlex.

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  12. Boosting Lipofection Efficiency Through Enhanced Membrane Fusion Mechanisms.International journal of molecular sciences · 2024
    Review
  13. Carbapenem-ResistantNanomaterials (Basel, Switzerland) · 2024
    Article
  14. Article
  15. Article
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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 1 institution in 1 country.

Masaru NishinoDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.ORCID 0000-0001-7080-8329
Ibu MatsuzakiDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Fidele Y MusangileDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Yuichi TakahashiDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Yoshifumi IwahashiDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Kenji WarigayaDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Yuichi KinoshitaDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Fumiyoshi KojimaDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Shin-Ichi MurataDepartment of Human Pathology, Wakayama Medical University, Wakayama, Japan.
Wakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diagnosis of patients with malignancies relies on the results of a clinical cytological examination. To enhance the diagnostic qualities of cytological examinations, it is important to have a detailed analysis of the cell's characteristics. There is, therefore, a need for developing a new auxiliary method for cytological diagnosis. In this study, we focused on studying the charge of the cell membrane surface of fixed cells, which is one of important cell's characteristics. Although fixed cells lose membrane potential which is observed in living cells owing to ion dynamics, we hypothesized that fixed cells still have a cell membrane surface charge due to cell membrane components and structure. We used 5 cell lines in this study (ARO, C32TG, RT4, TK, UM-UC-14). After fixation with CytoRich Red, we measured the cell membrane surface charge of fixed cells in solution using zeta potential measurements and fixed cells on glass slides, visualizing it using antibody-labeled beads and positively-charged beads. Furthermore, we measured the cell membrane surface charge of fixed cells under different conditions, such as different solution of fixative, ion concentration, pH, and pepsin treatments. The zeta potential measurements and visualization using the beads indicated that the cell membrane surface of fixed cells was negatively charged, and also that the charge varied among fixed cells. The charge state was affected by the different treatments. Moreover, the number of cell-bound beads was small in interphase, anaphase, and apoptotic cells. We concluded that the negative cell membrane surface charge was influenced by the three-dimensional structure of proteins as well as the different types of amino acids and lipids on the cell membrane. Thus, cell surface charge visualization can be applied as a new auxiliary method for clinical cytological diagnosis. This is the first systematic report of the cell membrane surface charge of fixed cells.

Indexed as

CytodiagnosisAnaphaseApoptosisCell CycleCell DivisionCell LineCell MembraneCells, CulturedFixativesHumansMembrane PotentialsPepsin ASurface PropertiesFixativesPepsin A

Identifiers

PMID32702063
PMCPMC7377470
OpenAlexW3044516346

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LicenceCC BY
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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.