Evidence map›Paper›PMID 28028137›Full record

ArticleJournal of the American Society of Nephrology : JASN2017

Diversification of Cell Lineages in Ureter Development.

Tobias Bohnenpoll, Sarah Feraric, Marvin Nattkemper, Anna-Carina Weiss, Carsten Rudat, Max Meuser, Mark-Oliver Trowe, Andreas Kispert

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. A knock inbioRxiv : the preprint server for biology · 2026
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  14. In focus in HCB.Histochemistry and cell biology · 2022
    Article
  15. Article
  16. Urothelial progenitors in development and repair.Pediatric nephrology (Berlin, Germany) · 2022
    Review
  17. Article
  18. Review
  19. Review
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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.

Tobias BohnenpollInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Sarah FeraricInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Marvin NattkemperInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Anna-Carina WeissInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Carsten RudatInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Max MeuserInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Mark-Oliver TroweInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.
Andreas KispertInstitut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany kispert.andreas@mh-hannover.de.
Medizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mammalian ureter consists of a mesenchymal wall composed of smooth muscle cells and surrounding fibrocytes of the tunica adventitia and the lamina propria and an inner epithelial lining composed of layers of basal, intermediate, and superficial cells. How these cell types arise from multipotent progenitors is poorly understood. Here, we performed marker analysis, cell proliferation assays, and genetic lineage tracing to define the lineage relations and restrictions of the mesenchymal and epithelial cell types in the developing and mature mouse ureter. At embryonic day (E) 12.5, the mesenchymal precursor pool began to subdivide into an inner and outer compartment that began to express markers of smooth muscle precursors and adventitial fibrocytes, respectively, by E13.5. Smooth muscle precursors further diversified into lamina propria cells directly adjacent to the ureteric epithelium and differentiated smooth muscle cells from E16.5 onwards. Uncommitted epithelial progenitors of the ureter differentiated into intermediate cells at E14.5. After stratification into two layers at E15.5 and three cell layers at E18.5, intermediate cells differentiated into basal cells and superficial cells. In homeostasis, proliferation of all epithelial and mesenchymal cell types remained low but intermediate cells still gave rise to basal cells, whereas basal cells divided only into basal cells. These studies provide a framework to further determine the molecular mechanisms of cell differentiation in the tissues of the developing ureter.

Indexed as

AnimalsCell DifferentiationCell LineageEpithelial CellsMesodermMiceMuscle, SmoothUretergenetics and developmentkidney developmentmolecular geneticsrenal cell biologyrenal developmentureteric bud

Identifiers

PMID28028137
PMCPMC5461796
OpenAlexW2567602392

What OpenQuestion holds

Textmetadata
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.