Evidence map›Paper›PMID 30921357›Full record

ArticlePloS one2019

A novel electron emission-based cell culture device promotes cell proliferation and differentiation of pre-osteoblastic MC3T3-E1 cells.

Fumiaki Sugimori, Hiroyuki Hirakawa, Ai Tsutsui, Hiroyuki Yamaji, Shohei Komaru, Mai Takasaki, Tadashi Iwamatsu, Toshimasa Uemura, Yo Uemura, Kenichi Morita and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

Fumiaki SugimoriAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.ORCID 0000-0002-0588-6117
Hiroyuki HirakawaAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.
Ai TsutsuiAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.
Hiroyuki YamajiAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.
Shohei KomaruAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.
Mai TakasakiAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.
Tadashi IwamatsuAdvanced Technology Development Unit, Business Solution Business Unit, SHARP CORPORATION, Yamatokoriyama, Nara, Japan.ORCID 0000-0001-7670-1426
Toshimasa UemuraCell Culture Marketing & Research Center, JTEC COOPERATION, Ibaraki, Osaka, Japan.
Yo UemuraCell Culture Marketing & Research Center, JTEC COOPERATION, Ibaraki, Osaka, Japan.
Kenichi MoritaCell Culture Marketing & Research Center, JTEC COOPERATION, Ibaraki, Osaka, Japan.
Takashi TsumuraCell Culture Marketing & Research Center, JTEC COOPERATION, Ibaraki, Osaka, Japan.
National Institute of Technology, Nara College · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this report we demonstrate the effect of a novel electron emission-based cell culture device on the proliferation and differentiation of pre-osteoblastic MC3T3-E1 cells. Our device has an electron emission element that allows, for the first time, stable emission of electrons into an atmosphere. Atmospheric electrons react with gas molecules to generate radicals and negative ions, which induce a variety of biochemical reactions in the attached cell culture system. In this study, we demonstrated the effect of this new electron emission-based cell culture device on cell proliferation and differentiation using pre-osteoblastic MC3T3-E1 cells. Electron emission stimulation (EES) was applied directly to culture medium containing plated cells, after which the number of living cells, the mRNA levels of osteogenesis-related genes, and the alkaline phosphatase (ALP) activity were evaluated. The growth rate of EES-exposed cells increased by approximately 20% in comparison with unexposed control cells. We also found the mRNA levels of osteogenic specific genes such as collagen type I α-1, core-binding factor α-1, and osteocalcin to be up-regulated following EES. ALP activity, a marker for osteogenic activity, was significantly enhanced in EES-treated cells. Furthermore, reactive oxygen species generated by EES were measured to determine their effect on MC3T3-E1 cells. These results suggest that our new electron emission-based cell culture device, while providing a relatively weak stimulus in comparison with atmospheric plasma systems, promotes cell proliferation and differentiation. This system is expected to find application in regenerative medicine, specifically in relation to bone regeneration.

Indexed as

Cell ProliferationOsteogenesisAnimalsAntigens, DifferentiationCell Culture TechniquesCell LineMiceOsteoblastsPlasma GasesReactive Oxygen SpeciesAntigens, DifferentiationPlasma GasesReactive Oxygen Species

Identifiers

PMID30921357
PMCPMC6438582
OpenAlexW2927321890

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.