Evidence map›Paper›PMID 17095600›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Oligozoospermia with normal fertility in male mice lacking the androgen receptor in testis peritubular myoid cells.

Caixia Zhang, Shuyuan Yeh, Yen-Ta Chen, Cheng-Chia Wu, Kuang-Hsiang Chuang, Hung-Yun Lin, Ruey-Sheng Wang, Yu-Jia Chang, Chamindrani Mendis-Handagama, Liquan Hu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
11.5field-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

50 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Androgen Actions in the Testis and the Regulation of Spermatogenesis.Advances in experimental medicine and biology · 2021
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Clinical significance of androgen secretion disorders in men with a malignancy.Medical oncology (Northwood, London, England) · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Genetic ablation of androgen receptor signaling in fetal Leydig cell lineage affects Leydig cell functions in adult testis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  20. Review
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

12 authors at 6 institutions in 3 countries.

Caixia ZhangGeorge Whipple Laboratory for Cancer Research, Department of Pathology, University of Rochester, Rochester, NY 14642, USA.
Shuyuan Yeh
Yen-Ta Chen
Cheng-Chia Wu
Kuang-Hsiang Chuang
Hung-Yun Lin
Ruey-Sheng Wang
Yu-Jia Chang
Chamindrani Mendis-Handagama
Liquan Hu
Henry Lardy
Chawnshang Chang
University of Rochester · USChang Gung University · TWInstitute of Clinical Research · USUniversity of Tennessee at Knoxville · USUniversity of Wisconsin–Madison · USWuhan University · CN

Funding

Suppression of Androgen Receptor by PTENR01DK060948 · NIDDK · UNIVERSITY OF ROCHESTER · PI CHANG, CHAWNSHANG · 2002 to 2006
$1.4M
MAP Kinase Signal on AR and AR coregulatorsR01DK060912 · NIDDK · UNIVERSITY OF ROCHESTER · PI YEH, SHUYUAN · 2001 to 2004
$1.1M
NIDDK NIH HHS DK60912NIDDK NIH HHS DK60948NIDDK NIH HHS R01 DK060912NIDDK NIH HHS R01 DK060948
6 · The paper itself

Abstract

Androgens and the androgen receptor (AR) play important roles in the testes. Previously we have shown that male total AR knockout (T-AR-/y) mice revealed incomplete germ cell development and lowered serum testosterone levels, which resulted in azoospermia and infertility. However, the consequences of AR loss in particular types of testicular cells remain unclear. Using a Cre-loxP conditional knockout strategy, we generated a tissue-selective knockout mouse with the AR gene deleted in testis peritubular myoid cells (PM-AR-/y). Phenotype analyses showed that PM-AR-/y mice were indistinguishable from WT AR (AR+/y) mice with the exception of smaller testes size. PM-AR-/y mice have serum testosterone concentrations comparable with AR+/y mice. PM-AR-/y mice have oligozoospermia in the epididymis; however, fertility was normal. Although normal germ cell distribution ratio was found, total germ cell number decreased in PM-AR-/y mice. Further mechanistic studies demonstrated that PM-AR-/y mice have defects in the expression of Sertoli cells' functional marker genes such as tranferrin, epidermal fatty acid-binding protein, androgen-binding protein, and other junction genes including occludin, testin, nectin, zyxin, vinculin, laminingamma3, gelsolin, connection43, and N-cadherin. Furthermore, there were defects in peritubular myoid cell contractility-related genes such as endothelin-1, endothelin receptor A and B, adrenomedullin, adrenomedullin receptor, and vasopressin receptor 1a. Together, our PM-AR-/y mice provide in vivo evidence for the requirement of functional AR in peritubular myoid cells to maintain normal Sertoli cells function and peritubular myoid cell contractility, thus ensuring normal spermatogenesis and sperm output.

Indexed as

FertilityOligospermiaAnimalsApoptosisFemaleFollicle Stimulating HormoneGerm CellsLuteinizing HormoneMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicOrgan SizeReceptors, AndrogenSertoli CellsFollicle Stimulating HormoneLuteinizing HormoneReceptors, AndrogenTestosterone

Identifiers

PMID17095600
PMCPMC1693813
OpenAlexW2069511698

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.