Evidence map›Paper›PMID 20650878›Full record

ArticleBiology of reproduction2010

Retinoic acid availability drives the asynchronous initiation of spermatogonial differentiation in the mouse.

Elizabeth M Snyder, Christopher Small, Michael D Griswold

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Isolation of Homogeneous Sub-populations of Spermatocytes from Mouse Testis.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  7. Article
  8. Identification and Expression Pattern ofAnimals : an open access journal from MDPI · 2022
    Article
  9. Article
  10. Unique metabolic phenotype and its transition during maturation of juvenile male germ cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Retinoic acid signaling pathways.Development (Cambridge, England) · 2019
    Review
  17. Retinoic acid signaling and the cycle of the seminiferous epithelium.Current opinion in endocrine and metabolic research · 2019
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Elizabeth M SnyderSchool of Molecular Biosciences, Washington State University, Pullman, Washington 99164, USA.
Christopher Small
Michael D Griswold
Washington State University · US

Funding

Spermatogonial Stem Cell Self-Renewal and DifferentiationU54HD042454 · NICHD · UNIVERSITY OF WASHINGTON · PI AMORY, JOHN K. · 2002 to 2016
$26.9M
Hormonal Regulation Sertoli Cell MaturationR01HD010808 · NICHD · WASHINGTON STATE UNIVERSITY · PI MICHAEL D GRISWOLD · 1985 to 2026
$6.0M
HORMONAL REGULATION OF SERTOLI CELL MATURATIONR37HD010808 · NICHD · WASHINGTON STATE UNIVERSITY · PI GRISWOLD, MICHAEL D · 1997 to 2006
$1.8M
NICHD NIH HHS HD10808NICHD NIH HHS R01 HD010808NICHD NIH HHS R37 HD010808NICHD NIH HHS U54 HD042454
6 · The paper itself

Abstract

Throughout the reproductive lifespan of most male mammals, sperm production is constant because of the regulated differentiation of spermatogonia. Retinoic acid (RA) and a downstream target, Stra8, are required for complete spermatogenesis. To examine the role of RA in initiating spermatogonial differentiation, a transgenic mouse model expressing beta-galactosidase under the control of an RA response element was used. Cells in the neonatal testis undergoing active RA signaling were visualized by beta-galactosidase activity, the relationship between RA and differentiation determined, and the role of RA-degrading enzymes in regulating RA demonstrated. Beta-galactosidase activity was found to be predominantly associated with differentiating, premeiotic germ cells and to be distributed nonuniformly throughout the seminiferous tubules. Additionally, beta-galactosidase activity in premeiotic germ cells colocalized with STRA8 protein and was induced in germ cells with exogenous RA treatment. The RA-degrading enzyme, CYP26B1, was found to have germ cell localization and nonuniform distribution between tubules via immunohistochemistry. Treatment with a CYP26 enzyme inhibitor resulted in an increased number of germ cells with both beta-galactosidase activity and STRA8 protein and an increase in the expression of genes associated with differentiation and reduced expression of a gene associated with undifferentiated germ cells. These results show the action of RA in a subset of spermatogonia leads to nonuniform initiation of differentiation throughout the neonatal testis, potentially mediated through the action of CYP26 enzymes. Thus, the presence of RA is a likely driving factor in the initiation of spermatogonial differentiation and may result in asynchronous spermatogenesis.

Indexed as

SpermatogenesisAdaptor Proteins, Signal TransducingAgingAnimalsAnimals, NewbornAntigens, DifferentiationCytochrome P-450 Enzyme InhibitorsCytochrome P-450 Enzyme SystemDown-RegulationEnzyme InhibitorsGenes, ReporterMaleMiceMice, TransgenicOrgan SpecificityProteinsAdaptor Proteins, Signal TransducingAntigens, DifferentiationCyp26b1 protein, mouseCytochrome P-450 Enzyme InhibitorsCytochrome P-450 Enzyme SystemEnzyme InhibitorsProteinsRetinoic Acid 4-HydroxylaseStra8 protein, mouseTretinoin

Identifiers

PMID20650878
PMCPMC2959108
OpenAlexW2015729941

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.