Evidence map›Paper›PMID 21298309›Full record

ArticleJournal of artificial organs : the official journal of the Japanese Society for Artificial Organs2011

Induction of putative stratified epithelial progenitor cells in vitro from mouse-induced pluripotent stem cells.

Miharu Sakurai, Ryuhei Hayashi, Tomofumi Kageyama, Masayuki Yamato, Kohji Nishida

Abstract read
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In one paragraph

Article in Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Progress in corneal wound healing.Progress in retinal and eye research · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Journal of Artificial Organs 2011: the year in review.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2012
    Review
  18. Article
  19. 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

5 authors at 2 institutions in 1 country.

Miharu SakuraiDepartment of Ophthalmology, Tohoku University School of Medicine, 1-1 Seiryomachi, Aoba-ku, Sendai, 980-8574, Japan.
Ryuhei Hayashi
Tomofumi Kageyama
Masayuki Yamato
Kohji Nishida
Tohoku University · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induced pluripotent stem (iPS) cells generally exhibit a normal karyotype, are transcriptionally and epigenetically similar to embryonic stem (ES) cells, and maintain the potential to differentiate into derivatives of all germ layers. Recently, the use of different types of cell or tissue derived from iPS cells for transplantation has become a possibility. However, the differentiation of epithelial lineages from iPS cells has not yet been demonstrated. We attempted to establish a culture technique for the induction of epithelial progenitors from mouse iPS cells. Mouse iPS cells were cultured on dishes coated with type IV collagen in keratinocyte culture medium (KCM) supplemented with or without bone morphogenic protein-4 (BMP-4) or combined with pretreatment of retinoic acid (RA) and BMP-4 in the undifferentiated state. Markers for undifferentiated cells (Oct3/4, Nanog) and for differentiation (p63, cytokeratin14) were analyzed by immunofluorescence staining and real-time RT-PCR. Putative epithelial progenitors were successfully induced in vitro from iPS cells. These progenitors expressed p63, a transcription factor necessary for maintenance of regenerative epithelia and cytokeratin 14 constitutively present in the basal layer of stratified epithelia. Enhancement of putative epithelial progenitor commitment was observed when cultured in KCM with BMP-4 following pretreatment of RA and BMP-4. The differentiation efficiency of putative epithelial progenitors from iPS cell cultures was similar to that of ES cell cultures. This report is the first to demonstrate in vitro differentiation of iPS cells into putative epithelial progenitors. These iPS-derived putative epithelial progenitors provide a powerful tool for understanding the mechanisms of epithelial lineage differentiation.

Indexed as

Analysis of VarianceAnimalsBone Morphogenetic Protein 4Cell DifferentiationCells, CulturedEpithelial CellsFluorescent Antibody TechniqueHomeodomain ProteinsImmunohistochemistryInduced Pluripotent Stem CellsKeratin-14MiceNanog Homeobox ProteinOctamer Transcription Factor-3PhosphoproteinsReverse Transcriptase Polymerase Chain ReactionBone Morphogenetic Protein 4Homeodomain ProteinsKeratin-14Nanog Homeobox ProteinNanog protein, mouseOctamer Transcription Factor-3PhosphoproteinsTrans-ActivatorsTretinoinTrp63 protein, mouse

Identifiers

PMID21298309
OpenAlexW2060535554

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.