Evidence map›Paper›PMID 24615934›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2014

Expression of genomic functional estrogen receptor 1 in mouse sertoli cells.

Jing Lin, Jia Zhu, Xian Li, Shengqiang Li, Zijian Lan, Jay Ko, Zhenmin Lei

Open access · bronzeAbstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Toxicological effects of bioactive peptide fractions obtained fromThe journal of venomous animals and toxins including tropical diseases · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Estrogens in Male Physiology.Physiological reviews · 2017
    Review
  11. Article
  12. Article
  13. 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

7 authors at 3 institutions in 1 country.

Jing LinDepartment of OB/GYN & Women's Health, University of Louisville School of Medicine, Louisville, KY, USA.
Jia ZhuDepartment of OB/GYN & Women's Health, University of Louisville School of Medicine, Louisville, KY, USA.
Xian LiDepartment of OB/GYN & Women's Health, University of Louisville School of Medicine, Louisville, KY, USA.
Shengqiang LiDepartment of OB/GYN & Women's Health, University of Louisville School of Medicine, Louisville, KY, USA.
Zijian LanDivision of Life Sciences, Alltech, Nicholasville, KY, USA.
Jay KoDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Zhenmin LeiDepartment of OB/GYN & Women's Health, University of Louisville School of Medicine, Louisville, KY, USA zhenmin.lei@louisville.edu.
University of Louisville · USAlltech (United States) · USUniversity of Illinois Urbana-Champaign · US

Funding

The Mechanism of Cryptorchidism in LH Receptor Knockout AnimalsR01HD057501 · NICHD · UNIVERSITY OF LOUISVILLE · PI LEI, ZHENMIN · 2008 to 2012
$1.4M
NICHD NIH HHS R01 HD057501NICHD NIH HHS R01-HD057501
6 · The paper itself

Abstract

There is no consensus whether Sertoli cells express estrogen receptor 1 (Esr1). Reverse transcription-polymerase chain reaction, Western blot, and immunofluorescence demonstrated that mouse Sertoli cell lines, TM4, MSC-1, and 15P-1, and purified primary mouse Sertoli cells (PSCs) contained Esr1 messenger RNA and proteins. Incubation of Sertoli cells with 17β-estradiol (E2) or ESR1 agonist stimulated the expression of an estrogen responsive gene Greb1, which was prevented by ESR inhibitor or ESR1 antagonist. Overexpression of Esr1 in MSC-1 enhanced E2-induced Greb1 expression, while knockdown of Esr1 by small interfering RNA in TM4 attenuated the response. Furthermore, E2-induced Greb1 expression was abolished in the PSCs isolated from Amh-Cre/Esr1-floxed mice in which Esr1 in Sertoli cells were selectively deleted. Chromatin immunoprecipitation assays indicated that E2-induced Greb1 expression in Sertoli cells was mediated by binding of ESR1 to estrogen responsive elements. In summary, ligand-dependent nuclear ESR1 was present in mouse Sertoli cells and mediates a classical genomic action of estrogens.

Indexed as

AnimalsCell LineDose-Response Relationship, DrugEstradiolEstrogen Receptor alphaEstrogen Receptor betaEstrogensGene Expression RegulationMaleMice, KnockoutRNA InterferenceRNA, MessengerSertoli CellsTime FactorsTransfectionEstradiolEstrogen Receptor alphaEstrogen Receptor betaEstrogensRNA, MessengerEsr1estrogengene regulationmouseSertoli cellstestis

Identifiers

PMID24615934
PMCPMC4212333
OpenAlexW2056635486

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.