Evidence map›Paper›PMID 29408990›Full record

ArticleBiology of reproduction2018

Leydig cell genes change their expression and association with polysomes in a stage-specific manner in the adult mouse testis.

Estela J Jauregui, Debra Mitchell, Savanna M Garza, Traci Topping, Cathryn A Hogarth, Michael D Griswold

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2018. 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
2.0field-weighted citation impact, top 14% 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, 16 citations in OpenAlex.

  1. Review
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  6. Synchronizing spermatogenesis in the mouse.Biology of reproduction · 2022
    Article
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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

6 authors at 1 institution in 1 country.

Estela J JaureguiSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Debra MitchellSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Savanna M GarzaSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Traci ToppingSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Cathryn A HogarthSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Michael D GriswoldSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman, Washington, USA.
Washington State University · US

Funding

Hormonal Regulation Sertoli Cell MaturationR01HD010808 · NICHD · WASHINGTON STATE UNIVERSITY · PI MICHAEL D GRISWOLD · 1985 to 2026
$6.0M
NICHD NIH HHS R01 HD010808
6 · The paper itself

Abstract

Spermatogenesis in mammals occurs in a very highly organized manner within the seminiferous epithelium regulated by different cell types in the testis. Testosterone produced by Leydig cells regulates blood-testis barrier formation, meiosis, spermiogenesis, and spermiation. However, it is unknown whether Leydig cell function changes with the different stages of the seminiferous epithelium. This study utilized the WIN 18,446 and retinoic acid (RA) treatment regime combined with the RiboTag mouse methodology to synchronize male germ cell development and allow for the in vivo mapping of the Leydig cell translatome across the different stages of one cycle of the seminiferous epithelium. Using microarrays analysis, we identified 11 Leydig cell-enriched genes that were expressed in stage-specific manner such as the glucocorticoid synthesis and transport genes, Cyp21a1 and Serpina6. In addition, there were nine Leydig cell transcripts that change their association with polysomes in correlation with the different stages of the spermatogenic cycle including Egr1. Interestingly, the signal intensity of EGR1 and CYP21 varied among Leydig cells in the adult asynchronous testis. However, testosterone levels across the different stages of germ cell development did not cycle. These data show, for the first time, that Leydig cell gene expression changes in a stage-specific manner during the cycle of the seminiferous epithelium and indicate that a heterogeneous Leydig cell population exists in the adult mouse testis.

Indexed as

AnimalsBlood-Testis BarrierGene ExpressionLeydig CellsMaleMicePolyribosomesSeminiferous EpitheliumSpermatogenesisSteroid 21-HydroxylaseTestisTranscortinCyp21a1 protein, mouseSerpina6 protein, mouseSteroid 21-HydroxylaseTranscortin

Identifiers

PMID29408990
PMCPMC6692846
OpenAlexW2794070776

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.