Evidence map›Paper›PMID 22865373›Full record

ArticleEndocrinology2012

Identification, proliferation, and differentiation of adult Leydig stem cells.

Erin Stanley, Chieh-Yin Lin, Shiying Jin, June Liu, Chantal M Sottas, Renshan Ge, Barry R Zirkin, Haolin Chen

Abstract read
In one paragraph

Article in Endocrinology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
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

59 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Age-related testosterone decline: mechanisms and intervention strategies.Reproductive biology and endocrinology : RB&E · 2024
    Review
  8. Use ofFrontiers in toxicology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Behavior and Functional Roles of CD34International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Review
  17. TCF21Nature communications · 2021
    Article
  18. Article
  19. Article
  20. 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

8 authors.

Erin StanleyDepartment of Biochemistry and Molecular Biology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland 21205, USA.
Chieh-Yin Lin
Shiying Jin
June Liu
Chantal M Sottas
Renshan Ge
Barry R Zirkin
Haolin Chen

Funding

Aging and Leydig Cell FunctionR37AG021092 · NIA · JOHNS HOPKINS UNIVERSITY · PI ZIRKIN, BARRY R · 2006 to 2015
$4.0M
AGING AND LEYDIG CELL FUNCTIONR01AG021092 · NIA · JOHNS HOPKINS UNIVERSITY · PI ZIRKIN, BARRY R · 2002 to 2019
$3.1M
In Search of Stem Leydig Cells: Identification, Isolation & DevelopmentR01HD050570 · NICHD · POPULATION COUNCIL · PI GE, REN-SHAN · 2007 to 2011
$1.4M
Aging and Function of Stem Leyding CellsR01AG030598 · NIA · POPULATION COUNCIL · PI GE, REN-SHAN · 2007 to 2010
$1.3M
Antioxidant Defense System and Leydig Cell AgingR03AG026721 · NIA · JOHNS HOPKINS UNIVERSITY · PI CHEN, HAOLIN · 2006 to 2007
$161k
NIA NIH HHS R01 AG021092NIA NIH HHS R01 AG030598NIA NIH HHS R03 AG026721NIA NIH HHS R37 AG021092NIA NIH HHS R37 AG21092NICHD NIH HHS R01 HD050570
6 · The paper itself

Abstract

Leydig cells, the testosterone-producing cells of the adult testis, rarely turn over. However, their elimination with ethane dimethanesulfonate (EDS) is followed by the appearance of new, fully functional adult Leydig cells. The cells that give rise to the new Leydig cells have not been well characterized, and little is known about the mechanism by which they are regulated. We isolated cells expressing platelet-derived growth factor receptor-α, but not 3β-hydroxysteroid dehydrogenase (3β-HSD(neg)) from the testes of EDS-treated adult rats. Depending on conditions, these cells proliferated indefinitely or differentiated and produced testosterone. To localize these cells and to determine the effect of the testicular environment on their function, the seminiferous tubules and testicular interstitium were physically separated and cultured. During the first 72 h in culture, 3β-HSD(neg) cells on the tubule surfaces underwent divisions. Some of these cells later expressed 3β-HSD and produced testosterone. Removal of the newly formed 3β-HSD(pos) cells from the tubule surfaces with EDS, followed by further culture of the stripped tubules, resulted in the reappearance of testosterone-producing cells. These results, taken together, suggest that the precursors for newly formed Leydig cells are stem cells, with many if not all situated on the surfaces of the seminiferous tubules. Although normally quiescent, the stem cells are capable of self-renewal and differentiation. The development of the tubule culture system should provide a valuable in vitro approach to assess the role(s) of niche components on the function of adult Leydig stem cells despite their residing in a complex mammalian tissue.

Indexed as

Adult Stem CellsAnimalsCell DifferentiationCell ProliferationCells, CulturedLeydig CellsLuteinizing HormoneMaleRatsRats, Inbred BNTestosteroneLuteinizing HormoneTestosterone

Identifiers

PMID22865373
PMCPMC3512003

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.