Evidence map›Paper›PMID 33848015›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2021

LGR6 marks nephron progenitor cells.

Ravian L van Ineveld, Thanasis Margaritis, Berend A P Kooiman, Femke Groenveld, Hendrikus C R Ariese, Philip Lijnzaad, Hannah R Johnson, Jeroen Korving, Ellen J Wehrens, Frank Holstege and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Lgr6Genes & diseases · 2026
    Review
  2. Review
  3. Article
  4. LGR6 marks nephron progenitor cells.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
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

14 authors at 4 institutions in 1 country.

Ravian L van IneveldPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Thanasis MargaritisPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-4040-2015
Berend A P KooimanPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Femke GroenveldHubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center (UMC) Utrecht, Utrecht, The Netherlands.
Hendrikus C R AriesePrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Philip LijnzaadPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Hannah R JohnsonPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Jeroen KorvingHubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center (UMC) Utrecht, Utrecht, The Netherlands.
Ellen J WehrensPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Frank HolstegePrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Jacco van RheenenOncode Institute, Utrecht, The Netherlands.
Jarno DrostPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Anne C RiosPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Frank L BosPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-3811-8330
Oncode Institute · NLPrincess Máxima Center · NLRoyal Netherlands Academy of Arts and Sciences · NLThe Netherlands Cancer Institute · NL

Funding

European Research Council 648804
6 · The paper itself

Abstract

backgroundNephron progenitor cells (NPCs) undergo a stepwise process to generate all mature nephron structures. Mesenchymal to epithelial transition (MET) is considered a multistep process of NPC differentiation to ensure progressive establishment of new nephrons. However, despite this important role, to date, no marker for NPCs undergoing MET in the nephron exists.

resultsHere, we identify LGR6 as a NPC marker, expressed in very early cap mesenchyme, pre-tubular aggregates, renal vesicles, and in segments of S-shaped bodies, following the trajectory of MET. By using a lineage tracing approach in embryonic explants in combination with confocal imaging and single-cell RNA sequencing, we provide evidence for the multiple fates of LGR6+ cells during embryonic nephrogenesis. Moreover, by using long-term in vivo lineage tracing, we show that postnatal LGR6+ cells are capable of generating the multiple lineages of the nephrons.

conclusionsGiven the profound early mesenchymal expression and MET signature of LGR6

Indexed as

NephronsStem CellsCell DifferentiationMesodermOrganogenesis3D imagingfateLGR6lineage tracingmesenchymal to epithelial transitionnephron progenitor cells

Identifiers

PMID33848015
PMCPMC8597161
OpenAlexW3154754385

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.