Evidence map›Paper›PMID 25406395›Full record

ArticleDevelopment (Cambridge, England)2014

RBPJ in mouse Sertoli cells is required for proper regulation of the testis stem cell niche.

Thomas Xavier Garcia, Jaspreet Kaur Farmaha, Sean Kow, Marie-Claude Hofmann

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Sumoylation and its regulation in testicular Sertoli cells.Biochemical and biophysical research communications · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Characterization of rodent Sertoli cell primary cultures.Molecular reproduction and development · 2020
    Review
  17. Article
  18. Article
  19. Review
  20. Undifferentiated spermatogonia regulateFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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

4 authors at 2 institutions in 1 country.

Thomas Xavier GarciaDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Unit 1105, PO Box 301402, Houston, TX 77230-1402, USA Department of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA.
Jaspreet Kaur FarmahaDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Unit 1105, PO Box 301402, Houston, TX 77230-1402, USA Department of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA.
Sean KowDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Unit 1105, PO Box 301402, Houston, TX 77230-1402, USA Department of Biochemistry & Cell Biology, Rice University, PO Box 1892, MS-140, Houston, TX 77251-1892, USA.
Marie-Claude HofmannDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Unit 1105, PO Box 301402, Houston, TX 77230-1402, USA Department of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA mhofmann@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of Illinois Urbana-Champaign · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Research Training Program in Toxicology and Environmental HealthT32ES007326 · NIEHS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI Jodi A. Flaws · 2000 to 2026
$8.7M
Molecular Regulation of the Perinatal Male Germ Cell NicheR01HD081244 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HOFMANN, MARIE-CLAUDE CATHERINE · 2014 to 2018
$1.6M
Isolation and Characterization of Testis Stem CellsR01HD044543 · NICHD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI HOFMANN, MARIE-CLAUDE CATHERINE · 2005 to 2009
$1.4M
Role of HES/HEY family of proteins in mammalian spermatogenesisR21HD068989 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HOFMANN, MARIE-CLAUDE CATHERINE · 2011 to 2012
$423k
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NICHD NIH HHS R01 HD044543NICHD NIH HHS R01HD044543NICHD NIH HHS R01 HD081244NICHD NIH HHS R01HD081244NICHD NIH HHS R21 HD068989NICHD NIH HHS R21HD068989NIEHS NIH HHS T32 ES007326NIEHS NIH HHS T32ES007326
6 · The paper itself

Abstract

Stem cells are influenced by their surrounding microenvironment, or niche. In the testis, Sertoli cells are the key niche cells directing the population size and differentiation fate of spermatogonial stem cells (SSCs). Failure to properly regulate SSCs leads to infertility or germ cell hyperplasia. Several Sertoli cell-expressed genes, such as Gdnf and Cyp26b1, have been identified as being indispensable for the proper maintenance of SSCs in their niche, but the pathways that modulate their expression have not been identified. Although we have recently found that constitutively activating NOTCH signaling in Sertoli cells leads to premature differentiation of all prospermatogonia and sterility, suggesting that there is a crucial role for this pathway in the testis stem cell niche, a true physiological function of NOTCH signaling in Sertoli cells has not been demonstrated. To this end, we conditionally ablated recombination signal binding protein for immunoglobulin kappa J region (Rbpj), a crucial mediator of NOTCH signaling, in Sertoli cells using Amh-cre. Rbpj knockout mice had: significantly increased testis sizes; increased expression of niche factors, such as Gdnf and Cyp26b1; significant increases in the number of pre- and post-meiotic germ cells, including SSCs; and, in a significant proportion of mice, testicular failure and atrophy with tubule lithiasis, possibly due to these unsustainable increases in the number of germ cells. We also identified germ cells as the NOTCH ligand-expressing cells. We conclude that NOTCH signaling in Sertoli cells is required for proper regulation of the testis stem cell niche and is a potential feedback mechanism, based on germ cell input, that governs the expression of factors that control SSC proliferation and differentiation.

Indexed as

AnimalsCellular MicroenvironmentGene Expression Regulation, DevelopmentalImmunoglobulin J Recombination Signal Sequence-Binding ProteinImmunohistochemistryMaleMiceMice, KnockoutReal-Time Polymerase Chain ReactionReceptors, NotchSertoli CellsSignal TransductionSpermatogoniaStem CellsTestisImmunoglobulin J Recombination Signal Sequence-Binding ProteinRbpj protein, mouseReceptors, NotchFertilityMouseNOTCH signalingRBPJSpermatogenesisSpermatogonial stem cellTesticular microlithiasis

Identifiers

PMID25406395
PMCPMC4302926
OpenAlexW2322395793

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.