Evidence map›Paper›PMID 29183737›Full record

ArticleDevelopmental biology2018

Cross-platform single cell analysis of kidney development shows stromal cells express Gdnf.

Bliss Magella, Mike Adam, Andrew S Potter, Meenakshi Venkatasubramanian, Kashish Chetal, Stuart B Hay, Nathan Salomonis, S Steven Potter

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 98 citations in OpenAlex.

  1. Review
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  3. The transcription factor Tcf21 is necessary for adoption of cell fates byAmerican journal of physiology. Renal physiology · 2026
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  19. The origin and role of the renal stroma.Development (Cambridge, England) · 2021
    Review
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1 more citing papers are in PubMed but not listed here.

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.

Bliss MagellaCincinnati Children's Medical Center, Division of Developmental Biology, 3333 Burnet Ave., Cincinnati, OH 45229, USA.
Mike AdamCincinnati Children's Medical Center, Division of Developmental Biology, 3333 Burnet Ave., Cincinnati, OH 45229, USA.
Andrew S PotterCincinnati Children's Medical Center, Division of Developmental Biology, 3333 Burnet Ave., Cincinnati, OH 45229, USA.
Meenakshi VenkatasubramanianCincinnati Children's Medical Center, Division of Biomedical Informatics, 3333 Burnet Ave., Cincinnati OH 45229, USA.
Kashish ChetalCincinnati Children's Medical Center, Division of Biomedical Informatics, 3333 Burnet Ave., Cincinnati OH 45229, USA.
Stuart B HayCincinnati Children's Medical Center, Division of Biomedical Informatics, 3333 Burnet Ave., Cincinnati OH 45229, USA.
Nathan SalomonisCincinnati Children's Medical Center, Division of Biomedical Informatics, 3333 Burnet Ave., Cincinnati OH 45229, USA. Electronic address: nathan.salomonis@cchmc.org.
S Steven PotterCincinnati Children's Medical Center, Division of Developmental Biology, 3333 Burnet Ave., Cincinnati, OH 45229, USA. Electronic address: steve.potter@cchmc.org.
Cincinnati Children's Hospital Medical Center · US

Funding

Progenitor Cell Biology Consortium Administrative Coordinating CenterU01HL099997 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI TERRIN, MICHAEL L · 2009 to 2015
$29.9M
Proteomics CoreP50DK096418 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI DEVARAJAN, PRASAD · 2012 to 2021
$8.4M
Global Gene Expression Atlas of the Developing KidneyU01DK070251 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI POTTER, S. STEVEN · 2004 to 2009
$2.1M
Recombineering based analysis of Hox function in kidney developmentR01DK099995 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI POTTER, S. STEVEN · 2014 to 2017
$1.4M
NHLBI NIH HHS U01 HL099997NIDDK NIH HHS P50 DK096418NIDDK NIH HHS R01 DK099995NIDDK NIH HHS U01 DK070251
6 · The paper itself

Abstract

The developing kidney provides a useful model for study of the principles of organogenesis. In this report we use three independent platforms, Drop-Seq, Chromium 10x Genomics and Fluidigm C1, to carry out single cell RNA-Seq (scRNA-Seq) analysis of the E14.5 mouse kidney. Using the software AltAnalyze, in conjunction with the unsupervised approach ICGS, we were unable to identify and confirm the presence of 16 distinct cell populations during this stage of active nephrogenesis. Using a novel integrative supervised computational strategy, we were able to successfully harmonize and compare the cell profiles across all three technological platforms. Analysis of possible cross compartment receptor/ligand interactions identified the nephrogenic zone stroma as a source of GDNF. This was unexpected because the cap mesenchyme nephron progenitors had been thought to be the sole source of GDNF, which is a key driver of branching morphogenesis of the collecting duct system. The expression of Gdnf by stromal cells was validated in several ways, including Gdnf in situ hybridization combined with immunohistochemistry for SIX2, and marker of nephron progenitors, and MEIS1, a marker of stromal cells. Finally, the single cell gene expression profiles generated in this study confirmed and extended previous work showing the presence of multilineage priming during kidney development. Nephron progenitors showed stochastic expression of genes associated with multiple potential differentiation lineages.

Indexed as

AnimalsGene Expression ProfilingGene Expression Regulation, DevelopmentalGlial Cell Line-Derived Neurotrophic FactorHomeodomain ProteinsIn Situ HybridizationMesenchymal Stem CellsMiceMyeloid Ecotropic Viral Integration Site 1 ProteinNephronsTranscription FactorsGdnf protein, mouseGlial Cell Line-Derived Neurotrophic FactorHomeodomain ProteinsMeis1 protein, mouseMyeloid Ecotropic Viral Integration Site 1 ProteinSix2 protein, mouseTranscription FactorsGdnfICGSKidney developmentMultilineage primingScRNA-Seq

Identifiers

PMID29183737
PMCPMC5930237
OpenAlexW2768688513

What OpenQuestion holds

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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.