Evidence map›Paper›PMID 37507645›Full record

ArticleIn vitro cellular & developmental biology. Animal2023

Reversible suspension culture of human vascular smooth muscle cells using the functional biopolymer FP003.

Masashi Uchida, Rina Higashimoto, Takumi Hoshino, Tomomi Natori, Daisuke Hatanaka, Hisato Hayashi, Tatsuro Kanaki, Takaaki Suzuki, Itsuko Ishii

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2023. 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 38% 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, 1 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

9 authors at 2 institutions in 1 country.

Masashi UchidaGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan. masac-u@chiba-u.jp.ORCID http://orcid.org/0000-0002-3171-9208
Rina HigashimotoGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Takumi HoshinoGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Tomomi NatoriGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Daisuke HatanakaNissan Chemical Corporation, 5-1, Nihonbashi 2-Chome, Chuo-Ku, Tokyo, 103-6119, Japan.
Hisato HayashiNissan Chemical Corporation, 5-1, Nihonbashi 2-Chome, Chuo-Ku, Tokyo, 103-6119, Japan.
Tatsuro KanakiNissan Chemical Corporation, 5-1, Nihonbashi 2-Chome, Chuo-Ku, Tokyo, 103-6119, Japan.
Takaaki SuzukiGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Itsuko IshiiGraduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Chiba University · JPNissan Chemical Corporation (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human vascular smooth muscle cells (SMCs) are adherent cells, and they cannot survive without scaffolds in suspension culture. Here, we aimed to establish a suspension culture of SMCs using the functional biopolymer FP003 and to investigate the proliferation status of the cells. When SMCs were suspension cultured with FP003, their proliferation was inhibited with a viability of 75% until day 15. When SMCs were re-plated on plastic plates after suspension culture with FP003 for 48 h, the SMCs proliferated as in a normal plate culture. The SMCs cultured in suspension with FP003 showed a relatively low phosphorylation of retinoblastoma protein, low expression of cyclin D1, high proportion of G0/G1 phase cells, low proportion of S phase cells, and no obvious signs of apoptosis, indicating that this culture system inhibited progression from the G1 to S phase. This growth arrest was a reversible property that showed no significant changes in the expressions of the marker proteins α-smooth muscle actin and smooth muscle myosin heavy chain. These results suggest that human SMCs can be stably cultured in suspension with FP003 without losing their characteristics when they are cultured on plastic plates again.

Indexed as

Muscle, Smooth, VascularProteinsAnimalsBiopolymersCells, CulturedHumansMyocytes, Smooth MuscleSulfur CompoundsBiopolymersFP-025ProteinsSulfur CompoundsExtracellular matrixGellan gumPolysaccharideVascular smooth muscle cells

Identifiers

PMID37507645
OpenAlexW4385350702

What OpenQuestion holds

Textmetadata
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.