Evidence map›Paper›PMID 24335651›Full record

ArticleNature cell biology2014

Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney.

M Takasato, P X Er, M Becroft, J M Vanslambrouck, E G Stanley, A G Elefanty, M H Little

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 358 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
358citing papers in PubMed, 1 pooled it
29.2field-weighted citation impact, top 1% 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

358 citing papers in PubMed, 1 synthesis or guideline pooled it, 707 citations in OpenAlex.

  1. Organoids: a systematic review of ethical issues.Stem cell research & therapy · 2022
    Pooled it
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  17. Current Progress of Tissue Engineering With Stem Cells in Urology Updated Review in 2025.International journal of urology : official journal of the Japanese Urological Association · 2025
    Review
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298 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

M TakasatoInstitute for Molecular Bioscience, The University of Queensland, St Lucia 4072, Queensland, Australia.
P X ErInstitute for Molecular Bioscience, The University of Queensland, St Lucia 4072, Queensland, Australia.
M BecroftInstitute for Molecular Bioscience, The University of Queensland, St Lucia 4072, Queensland, Australia.
J M VanslambrouckInstitute for Molecular Bioscience, The University of Queensland, St Lucia 4072, Queensland, Australia.
E G Stanley1] Murdoch Childrens Research Institute, The Royal Children's Hospital, Flemington Road, Parkville 3052, Victoria, Australia [2] Department of Anatomy and Developmental Biology, Monash University, Wellington Road, Clayton 3800, Victoria, Australia.
A G Elefanty1] Murdoch Childrens Research Institute, The Royal Children's Hospital, Flemington Road, Parkville 3052, Victoria, Australia [2] Department of Anatomy and Developmental Biology, Monash University, Wellington Road, Clayton 3800, Victoria, Australia.
M H LittleInstitute for Molecular Bioscience, The University of Queensland, St Lucia 4072, Queensland, Australia.
University of Queensland · AURoyal Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the prevalence of end-stage renal disease rising 8% per annum globally, there is an urgent need for renal regenerative strategies. The kidney is a mesodermal organ that differentiates from the intermediate mesoderm (IM) through the formation of a ureteric bud (UB) and the interaction between this bud and the adjacent IM-derived metanephric mesenchyme (MM). The nephrons arise from a nephron progenitor population derived from the MM (ref. ). The IM itself is derived from the posterior primitive streak. Although the developmental origin of the kidney is well understood, nephron formation in the human kidney is completed before birth. Hence, there is no postnatal stem cell able to replace lost nephrons. In this study, we have successfully directed the differentiation of human embryonic stem cells (hESCs) through posterior primitive streak and IM under fully chemically defined monolayer culture conditions using growth factors used during normal embryogenesis. This differentiation protocol results in the synchronous induction of UB and MM that forms a self-organizing structure, including nephron formation, in vitro. Such hESC-derived components show broad renal potential ex vivo, illustrating the potential for pluripotent-stem-cell-based renal regeneration.

Indexed as

Cell DifferentiationCell LineageAnimalsBlastocyst Inner Cell MassCell AggregationCell Culture TechniquesEmbryonic Stem CellsFibroblast Growth Factor 9HumansKidneyMesodermMiceNephronsPrimitive StreakTime FactorsUreterFGF9 protein, humanFibroblast Growth Factor 9

Identifiers

PMID24335651
OpenAlexW2029706942

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.