Evidence map›Paper›PMID 26607719›Full record

ArticleBiology of reproduction2016

Mouse Spermatogenesis Requires Classical and Nonclassical Testosterone Signaling.

Corey Toocheck, Terri Clister, John Shupe, Chelsea Crum, Preethi Ravindranathan, Tae-Kyung Lee, Jung-Mo Ahn, Ganesh V Raj, Meena Sukhwani, Kyle E Orwig and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2016. 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
10.1field-weighted citation impact, top 2% 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, 116 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Single-Cell RNA Sequencing Reveals an Atlas of Hezuo Pig Testis Cells.International journal of molecular sciences · 2024
    Article
  5. Review
  6. Review
  7. Hormone Regulation in Testicular Development and Function.International journal of molecular sciences · 2024
    Review
  8. Article
  9. It puts the T's in fertility: testosterone and spermatogenesis.International journal of impotence research · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Current markers for infertility in men.JBRA assisted reproduction · 2021
    Article
  19. Review
  20. Androgen Actions in the Testis and the Regulation of Spermatogenesis.Advances in experimental medicine and biology · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Corey ToocheckCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Terri ClisterCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
John ShupeCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Chelsea CrumCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Preethi RavindranathanDepartment of Urology, University of Texas, Southwestern Medical Center at Dallas, Dallas, Texas.
Tae-Kyung LeeDepartment of Chemistry, University of Texas, Dallas, Richardson, Texas.
Jung-Mo AhnDepartment of Chemistry, University of Texas, Dallas, Richardson, Texas.
Ganesh V RajDepartment of Urology, University of Texas, Southwestern Medical Center at Dallas, Dallas, Texas.
Meena SukhwaniCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Kyle E OrwigCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
William H WalkerCenter for Research in Reproductive Physiology, Department of Obstetrics, Gynecology, and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania walkerw@pitt.edu.
Magee-Womens Research Institute · USUniversity of Pittsburgh · USThe University of Texas at Dallas · USThe University of Texas Southwestern Medical Center · US

Funding

Characterization of male germline stem cells in a rhesus model of infertilityR01HD055475 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI ORWIG, KYLE EDWIN · 2008 to 2012
$3.5M
Nongenomic Androgen Signaling in Sertolli CellsR01HD043143 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WALKER, WILLIAM H · 2003 to 2010
$1.8M
Nongenomic Androgen Signaling in Sertolli CellsR56HD043143 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WALKER, WILLIAM H · 2008 to 2008
$290k
NICHD NIH HHS HD055475NICHD NIH HHS HD43143NICHD NIH HHS R01 HD043143NICHD NIH HHS R01 HD055475NICHD NIH HHS R56 HD043143
6 · The paper itself

Abstract

Testosterone acts though the androgen receptor in Sertoli cells to support germ cell development (spermatogenesis) and male fertility, but the molecular and cellular mechanisms by which testosterone acts are not well understood. Previously, we found that in addition to acting through androgen receptor to directly regulate gene expression (classical testosterone signaling pathway), testosterone acts through a nonclassical pathway via the androgen receptor to rapidly activate kinases that are known to regulate spermatogenesis. In this study, we provide the first evidence that nonclassical testosterone signaling occurs in vivo as the MAP kinase cascade is rapidly activated in Sertoli cells within the testis by increasing testosterone levels in the rat. We find that either classical or nonclassical signaling regulates testosterone-mediated Rhox5 gene expression in Sertoli cells within testis explants. The selective activation of classical or nonclassical signaling pathways in Sertoli cells within testis explants also resulted in the differential activation of the Zbtb16 and c-Kit genes in adjacent spermatogonia germ cells. Delivery of an inhibitor of either pathway to Sertoli cells of mouse testes disrupted the blood-testis barrier that is essential for spermatogenesis. Furthermore, an inhibitor of nonclassical testosterone signaling blocked meiosis in pubertal mice and caused the loss of meiotic and postmeiotic germ cells in adult mouse testes. An inhibitor of the classical pathway caused the premature release of immature germ cells. Collectively, these observations indicate that classical and nonclassical testosterone signaling regulate overlapping and distinct functions that are required for the maintenance of spermatogenesis and male fertility.

Indexed as

AnimalsDNA-Binding ProteinsEnzyme InhibitorsFertilityHomeodomain ProteinsMaleMiceMice, Inbred C57BLMitogen-Activated Protein KinasesPromyelocytic Leukemia Zinc Finger ProteinProto-Oncogene Proteins c-kitRatsRats, Sprague-DawleyReceptors, AndrogenSertoli CellsSignal TransductionDNA-Binding ProteinsEnzyme InhibitorsHomeodomain ProteinsMitogen-Activated Protein KinasesPromyelocytic Leukemia Zinc Finger ProteinProto-Oncogene Proteins c-kitReceptors, AndrogenRhox5 protein, ratTestosteroneTranscription FactorsZBTB16 protein, ratandrogen receptorfertilitynongenomicSertoli celltestis

Identifiers

PMID26607719
PMCPMC4809556
OpenAlexW2222433283

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.