Evidence map›Paper›PMID 39817691›Full record

ArticleDevelopment (Cambridge, England)2025

Interplay of SHH, WNT and BMP4 signaling regulates the development of the lamina propria in the murine ureter.

Philipp Straube, Anja Beckers, Ulrich W H Jany, Florian Bergmann, Timo H-W Lüdtke, Carsten Rudat, Mark-Oliver Trowe, Imke Peters, Maximilian G Klopf, Tamrat M Mamo and 1 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

11 authors.

Philipp StraubeInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Anja BeckersInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Ulrich W H JanyInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-4506-3817
Florian BergmannInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Timo H-W LüdtkeInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Carsten RudatInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Mark-Oliver TroweInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Imke PetersInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Maximilian G KlopfInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0009-0003-1569-9205
Tamrat M MamoInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.
Andreas KispertInstitute of Molecular Biology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-8154-0257

Funding

Deutsche Forschungsgemeinschaft DFG KI728/8-2Deutsche Forschungsgemeinschaft DFG KI728/8-2, DFG KI728/9-2Hannover Medical School
6 · The paper itself

Abstract

In mammalian ureters, the lamina propria presents as a prominent layer of connective tissue underneath the urothelium. Despite its important structural and signaling functions, little is known how the lamina propria develops. Here, we show that in the murine ureter the lamina propria arises at late fetal stages and massively increases by fibrocyte proliferation and collagen deposition after birth. WNT, SHH, BMP4 and retinoic acid signaling are all active in the common mesenchymal progenitor of smooth muscle cells and lamina propria fibrocytes. However, around birth, the lamina propria becomes a target for epithelial WNT and SHH signals and a source of BMP4 and retinoic acid. SHH and WNT signaling promote lamina propria and smooth muscle cell differentiation and proliferation at fetal and early postnatal stages, whereas BMP4 signaling is required for early smooth muscle cell differentiation but not for its later maintenance. Our findings suggest that, in the presence of SHH and WNT signaling, it is the modulation of BMP4 signaling which is the major determinant for the segregation of lamina propria and smooth muscle cells.

Indexed as

Bone Morphogenetic Protein 4Hedgehog ProteinsMucous MembraneSignal TransductionUreterWnt ProteinsWnt Signaling PathwayAnimalsCell DifferentiationCell ProliferationGene Expression Regulation, DevelopmentalMiceMyocytes, Smooth MuscleTretinoinBmp4 protein, mouseBone Morphogenetic Protein 4Hedgehog ProteinsShh protein, mouseTretinoinWnt ProteinsDifferentiationLamina propriaOrganogenesisSignalingUreter

Identifiers

PMID39817691
PMCPMC11829765

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Registered trials

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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.