Evidence map›Paper›PMID 25710594›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2015

Research resource: the dynamic transcriptional profile of sertoli cells during the progression of spermatogenesis.

Céline Zimmermann, Isabelle Stévant, Christelle Borel, Béatrice Conne, Jean-Luc Pitetti, Pierre Calvel, Henrik Kaessmann, Bernard Jégou, Frédéric Chalmel, Serge Nef

Abstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
7.6field-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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pharmacogenetics of FSH Action in the Male.Frontiers in endocrinology · 2019
    Pooled it
  2. Testicular Gap (Animals : an open access journal from MDPI · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Etiology of Male Infertility: an Update.Reproductive sciences (Thousand Oaks, Calif.) · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. ThroughoutFrontiers in endocrinology · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

10 authors at 4 institutions in 2 countries.

Céline ZimmermannDepartment of Genetic Medicine and Development (C.Z., I.S., C.B., B.C., J.-L.P., P.C., S.N.), University of Geneva Medical School, 1211 Geneva 4, Switzerland; Center for Integrative Genomics (H.K.), University of Lausanne, Génopode, CH-1015 Lausanne, Switzerland; and Inserm U1085-IRSET (B.J., F.C.), Université de Rennes 1, Campus de Beaulieu, F-35042 Rennes, France.
Isabelle Stévant
Christelle Borel
Béatrice Conne
Jean-Luc Pitetti
Pierre Calvel
Henrik Kaessmann
Bernard Jégou
Frédéric Chalmel
Serge Nef
University of Geneva · CHInstitut de Recherche en Santé, Environnement et Travail · FRUniversité de Rennes · FRUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sertoli cells (SCs), the only somatic cells within seminiferous tubules, associate intimately with developing germ cells. They not only provide physical and nutritional support but also secrete factors essential to the complex developmental processes of germ cell proliferation and differentiation. The SC transcriptome must therefore adapt rapidly during the different stages of spermatogenesis. We report comprehensive genome-wide expression profiles of pure populations of SCs isolated at 5 distinct stages of the first wave of mouse spermatogenesis, using RNA sequencing technology. We were able to reconstruct about 13 901 high-confidence, nonredundant coding and noncoding transcripts, characterized by complex alternative splicing patterns with more than 45% comprising novel isoforms of known genes. Interestingly, roughly one-fifth (2939) of these genes exhibited a dynamic expression profile reflecting the evolving role of SCs during the progression of spermatogenesis, with stage-specific expression of genes involved in biological processes such as cell cycle regulation, metabolism and energy production, retinoic acid synthesis, and blood-testis barrier biogenesis. Finally, regulatory network analysis identified the transcription factors endothelial PAS domain-containing protein 1 (EPAS1/Hif2α), aryl hydrocarbon receptor nuclear translocator (ARNT/Hif1β), and signal transducer and activator of transcription 1 (STAT1) as potential master regulators driving the SC transcriptional program. Our results highlight the plastic transcriptional landscape of SCs during the progression of spermatogenesis and provide valuable resources to better understand SC function and spermatogenesis and its related disorders, such as male infertility.

Indexed as

TranscriptomeAnimalsGene Expression ProfilingMaleMiceMice, TransgenicSeminiferous TubulesSertoli CellsSpermatogenesis

Identifiers

PMID25710594
PMCPMC5414748
OpenAlexW2098523657

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.