Evidence map›Paper›PMID 26813041›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2016

Mosaic analysis of cell rearrangements during ureteric bud branching in dissociated/reaggregated kidney cultures and in vivo.

Kevin Leclerc, Frank Costantini

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Measurement of adhesion and traction of cells at high yield reveals an energetic ratchet operating during nephron condensation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Organ-Specific Branching Morphogenesis.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Article
  11. 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

2 authors at 1 institution in 1 country.

Kevin LeclercDepartment of Genetics and Development, Columbia University Medical Center, New York, NY.
Frank CostantiniDepartment of Genetics and Development, Columbia University Medical Center, New York, NY.
Columbia University Irving Medical Center · US

Funding

Branching Morphogenesis of Urinary Epithelia: from Genes to Cellular BehaviorsR01DK083289 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTANTINI, FRANKLIN D · 2009 to 2018
$4.9M
Genetic Control of Ureter and Kidney DevelopmentR01DK082715 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTANTINI, FRANKLIN D · 2009 to 2013
$3.1M
NIDDK NIH HHS 2R01DK083289NIDDK NIH HHS R01 DK082715NIDDK NIH HHS R01 DK083289
6 · The paper itself

Abstract

backgroundCell rearrangements mediated by GDNF/Ret signaling underlie the formation of the ureteric bud (UB) tip domain during kidney development. Whether FGF signaling also influences these rearrangements is unknown. Chimeric embryos are a powerful tool for examining the genetic controls of cellular behaviors, but generating chimeras by traditional methods is expensive and laborious. Dissociated fetal kidney cells can reorganize to form complex structures including branching UB tubules, providing an easier method to generate renal chimeras.

resultsCell behaviors in normal or chimeric kidney cultures were investigated using time-lapse imaging. In Spry1(-/-) ↔ wild-type chimeras, cells lacking Spry1 (a negative regulator of Ret and FGF receptor signaling) preferentially occupied the UB tips, as previously observed in traditional chimeras, thus validating this experimental system. In Fgfr2(UB-/-) ↔ wild-type chimeras, the wild-type cells preferentially occupied the tips. Independent evidence for a role of Fgfr2 in UB tip formation was obtained using Mosaic mutant Analysis with Spatial and Temporal control of Recombination (MASTR).

conclusionsDissociation and reaggregation of fetal kidney cells of different genotypes, with suitable fluorescent markers, provides an efficient way to analyze cell behaviors in chimeric cultures. FGF/Fgfr2 signaling promotes UB cell rearrangements that form the tip domain, similarly to GDNF/Ret signaling.

Indexed as

AnimalsCells, CulturedKidneyMiceMice, KnockoutSignal TransductionchimeraFGF receptor 2MASTRreceptor tyrosine kinaseSprouty1

Identifiers

PMID26813041
PMCPMC4803602
OpenAlexW2419758825

What OpenQuestion holds

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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.