Evidence map›Paper›PMID 37427413›Full record

ArticleTissue engineering. Part C, Methods2023

Improved Production of Induced Pluripotent Stem Cells Using Dot Pattern Culture Plates.

Yoshiki Nakashima, Hiroki Iguchi, Eiko Shimizu, Minh N T Le, Kenta Takakura, Yuta Nakamura, Teruhiko Yanagisawa, Rutvi Sanghavi, Satoshi Haneda, Masayoshi Tsukahara

Abstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 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
–field-weighted citation impact
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. 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

10 authors.

Yoshiki NakashimaResearch and Development Center, Kyoto University Center for iPS Cell Research and Application Foundation (CiRA Foundation), Kyoto, Japan.ORCID 0000-0003-1827-7609
Hiroki IguchiLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Eiko ShimizuResearch and Development Center, Kyoto University Center for iPS Cell Research and Application Foundation (CiRA Foundation), Kyoto, Japan.
Minh N T LeKyoto University iCeMS Institute for Integrated Cell-Material Sciences, Kyoto, Japan.
Kenta TakakuraLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Yuta NakamuraLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Teruhiko YanagisawaLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Rutvi SanghaviLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Satoshi HanedaLife Science Development Center Advanced Technology Institute R&D Center Corporate, SEKISUI CHEMICAL CO., LTD., Osaka, Japan.
Masayoshi TsukaharaResearch and Development Center, Kyoto University Center for iPS Cell Research and Application Foundation (CiRA Foundation), Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rate of cell proliferation is a crucial factor in cell production under good manufacturing practice (GMP) control. In this study, we identified a culture system for induced pluripotent cells (iPSCs) that supports cell proliferation and viability and maintains the cells in an undifferentiated state even at 8 days after seeding. This system involves the use of dot pattern culture plates that have been coated with a chemically defined scaffold which has high biocompatibility. Under cell starvation conditions, where medium exchange was not performed for 7 days or where the amount of medium exchange was reduced to half or a quarter, iPSC viability and lack of differentiation were maintained. The rate of cell viability in this culture system was greater than generally obtained by standard culture methods. The cells in this compartmentalized culture system could be induced to differentiate in a controlled and consistent manner: differentiation of endoderm occurred in a controlled and consistent manner: endoderm, mesoderm, and ectoderm could be consistently induced to differentiate in the cultures. In conclusion, we have developed a culture system that supports high viability in iPSCs and allows their controlled differentiation. This system has the potential for use in GMP-based production of iPSCs for clinical purposes.

Indexed as

Induced Pluripotent Stem CellsCell Culture TechniquesCell DifferentiationCulture MediaCulture Mediaculture systemdot pattern culture platesinduced pluripotent stem cells

Identifiers

PMID37427413
PMCPMC10517333

What OpenQuestion holds

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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.