Evidence map›Paper›PMID 23755150›Full record

ArticlePloS one2014

Kidney specific protein-positive cells derived from embryonic stem cells reproduce tubular structures in vitro and differentiate into renal tubular cells.

Ryuji Morizane, Toshiaki Monkawa, Shizuka Fujii, Shintaro Yamaguchi, Koichiro Homma, Yumi Matsuzaki, Hideyuki Okano, Hiroshi Itoh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Lineage tracing reveals KSPFrontiers in cell and developmental biology · 2026
    Article
  2. Review
  3. Human reconstructed kidney models.In vitro cellular & developmental biology. Animal · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Kidney Organoids: A Translational Journey.Trends in molecular medicine · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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.

Ryuji MorizaneDepartment of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Toshiaki Monkawa
Shizuka Fujii
Shintaro Yamaguchi
Koichiro Homma
Yumi Matsuzaki
Hideyuki Okano
Hiroshi Itoh
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Embryonic stem cells and induced pluripotent stem cells have the ability to differentiate into various organs and tissues, and are regarded as new tools for the elucidation of disease mechanisms as well as sources for regenerative therapies. However, a method of inducing organ-specific cells from pluripotent stem cells is urgently needed. Although many scientists have been developing methods to induce various organ-specific cells from pluripotent stem cells, renal lineage cells have yet to be induced in vitro because of the complexity of kidney structures and the diversity of kidney-component cells. Here, we describe a method of inducing renal tubular cells from mouse embryonic stem cells via the cell purification of kidney specific protein (KSP)-positive cells using an anti-KSP antibody. The global gene expression profiles of KSP-positive cells derived from ES cells exhibited characteristics similar to those of cells in the developing kidney, and KSP-positive cells had the capacity to form tubular structures resembling renal tubular cells when grown in a 3D culture in Matrigel. Moreover, our results indicated that KSP-positive cells acquired the characteristics of each segment of renal tubular cells through tubular formation when stimulated with Wnt4. This method is an important step toward kidney disease research using pluripotent stem cells, and the development of kidney regeneration therapies.

Indexed as

Cell DifferentiationAnimalsAntibodies, MonoclonalCadherinsCollagenDrug CombinationsEmbryonic Stem CellsEpithelial CellsExtracellular SpaceHepatocyte Growth FactorImmunohistochemistryInsulin-Like Growth Factor IKidney TubulesLamininMiceNIH 3T3 CellsAntibodies, MonoclonalCadherinsCdh16 protein, mouseCollagenDrug CombinationsHepatocyte Growth FactorInsulin-Like Growth Factor ILamininmatrigelProteinsProteoglycansWnt4 Protein

Identifiers

PMID23755150
PMCPMC3670839
OpenAlexW1966674393

What OpenQuestion holds

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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.