Evidence map›Paper›PMID 22698282›Full record

ArticleDevelopmental cell2012

FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.

Hila Barak, Sung-Ho Huh, Shuang Chen, Cécile Jeanpierre, Jelena Martinovic, Mélanie Parisot, Christine Bole-Feysot, Patrick Nitschké, Rémi Salomon, Corinne Antignac and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 185 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
185citing papers in PubMed, 1 pooled it
11.4field-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

185 citing papers in PubMed, 1 synthesis or guideline pooled it, 315 citations in OpenAlex.

  1. Pooled it
  2. Epigenetic regulation of kidney development.Nature reviews. Nephrology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. FGF family in health and disease.Molecular biomedicine · 2026
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

125 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 3 countries.

Hila BarakDepartment of Developmental Biology, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8103, St. Louis, MO 63110, USA.
Sung-Ho Huh
Shuang Chen
Cécile Jeanpierre
Jelena Martinovic
Mélanie Parisot
Christine Bole-Feysot
Patrick Nitschké
Rémi Salomon
Corinne Antignac
David M Ornitz
Raphael Kopan
Washington University in St. Louis · USHôpital Necker-Enfants Malades · FRDélégation Paris 5 · FRHôpital Antoine-Béclère · FRInserm · FRUniversité Paris Cité · FR

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Sensory Function CoreP30DC004665 · NIDCD · WASHINGTON UNIVERSITY · PI FADDIS, BRIAN T · 2001 to 2015
$8.0M
The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SILVA, MATTHEW J · 2009 to 2018
$5.7M
Washington University Center for Kidney Disease ResearchP30DK079333 · NIDDK · WASHINGTON UNIVERSITY · PI HAMMERMAN, MARC RANDALL · 2007 to 2011
$5.1M
ROLE OF NOTCH AND KIDNEY DEVELOPMENTR01DK066408 · NIDDK · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2004 to 2012
$3.4M
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NIAMS NIH HHS P30 AR057235NIAMS NIH HHS P30AR057235NIDCD NIH HHS P30 DC004665NIDCD NIH HHS P30DC04665NIDDK NIH HHS DK066408NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30DK052574NIDDK NIH HHS P30 DK079333NIDDK NIH HHS R01 DK066408
6 · The paper itself

Abstract

The identity of niche signals necessary to maintain embryonic nephron progenitors is unclear. Here we provide evidence that Fgf20 and Fgf9, expressed in the niche, and Fgf9, secreted from the adjacent ureteric bud, are necessary and sufficient to maintain progenitor stemness. Reduction in the level of these redundant ligands in the mouse led to premature progenitor differentiation within the niche. Loss of FGF20 in humans, or of both ligands in mice, resulted in kidney agenesis. Sufficiency was shown in vitro where Fgf20 or Fgf9 (alone or together with Bmp7) maintained isolated metanephric mesenchyme or sorted nephron progenitors that remained competent to differentiate in response to Wnt signals after 5 or 2 days in culture, respectively. These findings identify a long-sought-after critical component of the nephron stem cell niche and hold promise for long-term culture and utilization of these progenitors in vitro.

Indexed as

Cell DifferentiationAnimalsBone Morphogenetic Protein 7Congenital AbnormalitiesFemaleFibroblast Growth Factor 9Fibroblast Growth FactorsHumansKidneyKidney DiseasesMaleMesenchymal Stem CellsMiceMutationNephronsOrgan Culture TechniquesBMP7 protein, humanbmp7 protein, mouseBone Morphogenetic Protein 7FGF20 protein, humanFgf20 protein, mouseFGF9 protein, humanFgf9 protein, mouseFibroblast Growth Factor 9Fibroblast Growth Factors

Identifiers

PMID22698282
PMCPMC3376351
OpenAlexW2026527439

What OpenQuestion holds

Textmetadata
LicenceTDM
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.