Evidence map›Paper›PMID 26274378›Full record

ArticleJournal of visualized experiments : JoVE2015

Gene Transfection toward Spheroid Cells on Micropatterned Culture Plates for Genetically-modified Cell Transplantation.

Keiji Itaka, Satoshi Uchida, Akitsugu Matsui, Kayoko Yanagihara, Masaru Ikegami, Taisuke Endo, Takehiko Ishii, Kazunori Kataoka

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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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

8 authors at 1 institution in 1 country.

Keiji ItakaGraduate School of Medicine, Laboratory of Clinical Biotechnology, The University of Tokyo; itaka-ort@umin.net.
Satoshi UchidaGraduate School of Medicine, Laboratory of Clinical Biotechnology, The University of Tokyo.
Akitsugu MatsuiGraduate School of Medicine, Laboratory of Clinical Biotechnology, The University of Tokyo.
Kayoko YanagiharaGraduate School of Medicine, Laboratory of Clinical Biotechnology, The University of Tokyo.
Masaru IkegamiGraduate School of Medicine, Laboratory of Clinical Biotechnology, The University of Tokyo.
Taisuke EndoGraduate School of Engineering, Department of Materials Engineering, The University of Tokyo.
Takehiko IshiiGraduate School of Engineering, Department of Bioengineering, The University of Tokyo.
Kazunori KataokaGraduate School of Engineering, Department of Materials Engineering, The University of Tokyo.
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To improve the therapeutic effectiveness of cell transplantation, a transplantation system of genetically modified, injectable spheroids was developed. The cell spheroids are prepared in a culture system on micropatterned plates coated with a thermosensitive polymer. A number of spheroids are formed on the plates, corresponding to the cell adhesion areas of 100 µm diameter that are regularly arrayed in a two-dimensional manner, surrounded by non-adhesive areas that are coated by a polyethylene glycol (PEG) matrix. The spheroids can be easily recovered as a liquid suspension by lowering the temperature of the plates, and their structure is well maintained by passing them through injection needles with a sufficiently large caliber (over 27 G). Genetic modification is achieved by gene transfection using the original non-viral gene carrier, polyplex nanomicelle, which is capable of introducing genes into cells without disrupting the spheroid structure. For primary hepatocyte spheroids transfected with a luciferase-expressing gene, the luciferase is sustainably obtained in transplanted animals, along with preserved hepatocyte function, as indicated by albumin expression. This system can be applied to a variety of cell types including mesenchymal stem cells.

Indexed as

AnimalsCell AdhesionCell Culture TechniquesCell TransplantationGene ExpressionHepatocytesLuciferasesMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationPolyethylene GlycolsRatsRats, Sprague-DawleySpheroids, CellularTransfectionTransgenesLuciferasesPolyethylene Glycols

Identifiers

PMID26274378
PMCPMC4545087
OpenAlexW969299834

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.