Evidence map›Paper›PMID 31142573›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

Von Hippel-Lindau Acts as a Metabolic Switch Controlling Nephron Progenitor Differentiation.

Kasey Cargill, Shelby L Hemker, Andrew Clugston, Anjana Murali, Elina Mukherjee, Jiao Liu, Daniel Bushnell, Andrew J Bodnar, Zubaida Saifudeen, Jacqueline Ho and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2019. 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
1.3field-weighted citation impact, top 20% 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, 27 citations in OpenAlex.

  1. Epigenetic regulation of kidney development.Nature reviews. Nephrology · 2026
    Review
  2. Review
  3. Review
  4. Article
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  11. HIF in Gastric Cancer: Regulation and Therapeutic Target.Molecules (Basel, Switzerland) · 2022
    Review
  12. Article
  13. Article
  14. Metabolic programming of nephron progenitor cell fate.Pediatric nephrology (Berlin, Germany) · 2021
    Review
  15. Erythrocyte metabolism, oxygen delivery, and hypertensive kidney disease.International Journal of Cardiology. Hypertension · 2020
    Article
  16. Review
  17. Deletion of hypoxia-responsive microRNA-210 results in a sex-specific decrease in nephron number.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Kasey CargillRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Shelby L HemkerRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Andrew ClugstonRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Anjana MuraliRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Elina MukherjeeRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Jiao LiuSection of Pediatric Nephrology, Department of Pediatrics and.
Daniel BushnellRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Andrew J BodnarRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Zubaida SaifudeenSection of Pediatric Nephrology, Department of Pediatrics and.
Jacqueline HoRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Carlton M BatesRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Dennis KostkaRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Eric S GoetzmanRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Sunder Sims-LucasRangos Research Center, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania; simslucass@upmc.edu.
University of Pittsburgh · USUniversity of Pittsburgh Medical Center · USChildren's Hospital of Pittsburgh · USTulane University · US

Funding

Single Nephron and MetabolomicsP30DK079307 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2008 to 2022
$13.4M
Regulation of Peroxisomal Metabolism by Lysine AcylationR01DK090242 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GOETZMAN, ERIC S · 2011 to 2024
$5.4M
Renal and Epithelial Biology Training ProgramT32DK061296 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2002 to 2022
$3.1M
The Role of miR-17~92 in Nephron ProgenitorsR01DK103776 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HO, JACQUELINE · 2014 to 2018
$1.7M
Noom Coach for Bariatric SurgeryR44DK116370 · NIDDK · NOOM, INC. · PI HILDEBRANDT, THOMAS B, MICHAELIDES, ANDREAS · 2017 to 2019
$1.3M
Modeling the Dynamics of Genome-Scale Data Across TreesR01GM115836 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAPRA, JOHN ANTHONY, KOSTKA, DENNIS · 2015 to 2017
$1.1M
Renal Stroma Derived Endothelial Precursors are Critical for Renal DevelopmentK01DK096996 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SIMS-LUCAS, SUNDER · 2013 to 2017
$557k
Kidney derived endothelial progenitors play a critical role during kidney injuryR03DK110503 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SIMS-LUCAS, SUNDER · 2017 to 2018
$156k
Von Hippel-Lindau mediates nephron progenitor fate via regulation of metabolismF31DK113670 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CARGILL, KASEY · 2018 to 2019
$67k
NIDDK NIH HHS F31 DK113670NIDDK NIH HHS K01 DK096996NIDDK NIH HHS P30 DK079307NIDDK NIH HHS R01 DK090242NIDDK NIH HHS R01 DK103776NIDDK NIH HHS R03 DK110503NIDDK NIH HHS R44 DK116370NIDDK NIH HHS T32 DK061296NIGMS NIH HHS R01 GM115836
6 · The paper itself

Abstract

backgroundNephron progenitors, the cell population that give rise to the functional unit of the kidney, are metabolically active and self-renew under glycolytic conditions. A switch from glycolysis to mitochondrial respiration drives these cells toward differentiation, but the mechanisms that control this switch are poorly defined. Studies have demonstrated that kidney formation is highly dependent on oxygen concentration, which is largely regulated by von Hippel-Lindau (VHL; a protein component of a ubiquitin ligase complex) and hypoxia-inducible factors (a family of transcription factors activated by hypoxia).

methodsTo explore VHL as a regulator defining nephron progenitor self-renewal versus differentiation, we bred Six2-TGC

resultsBy embryonic day 15.5, kidneys of nephron progenitor cell-specific

conclusionsOur findings identify a novel role for VHL in mediating nephron progenitor differentiation through metabolic regulation, and suggest that VHL is required for normal kidney development.

Indexed as

AnimalsCell DifferentiationGene Expression RegulationGlycolysisHomeodomain ProteinsMiceMitochondriaNephronsStem CellsTranscription FactorsVon Hippel-Lindau Tumor Suppressor ProteinHomeodomain ProteinsSix2 protein, mouseTranscription FactorsVHL protein, mouseVon Hippel-Lindau Tumor Suppressor ProteinCellular differentiationGlycolysisHIF-1α metabolismNephron progenitorsVHL

Identifiers

PMID31142573
PMCPMC6622426
OpenAlexW2947789511

What OpenQuestion holds

Textmetadata
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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.