Evidence map›Paper›PMID 25093968›Full record

ArticleDevelopmental biology2014

Steroid signaling promotes stem cell maintenance in the Drosophila testis.

Yijie Li, Qing Ma, Christopher M Cherry, Erika L Matunis

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Single-cyst transcriptome analysis ofDevelopment (Cambridge, England) · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. 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

4 authors at 1 institution in 1 country.

Yijie LiDepartment of Cell Biology, 725 N. Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Qing MaDepartment of Cell Biology, 725 N. Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Christopher M CherryDepartment of Cell Biology, 725 N. Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Erika L MatunisDepartment of Cell Biology, 725 N. Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: matunis@jhmi.edu.
Johns Hopkins University · US

Funding

JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI AHIMA, REXFORD S. · 2013 to 2017
$9.7M
CONTROL OF STEM CELL FATE IN DROSOPHILA SPERMATOGENESISR01HD040307 · NICHD · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, ERIKA L · 2001 to 2014
$4.1M
Cellular plasticity in the Drosophila spermatogonial stem cell nicheR01HD052937 · NICHD · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, ERIKA L · 2007 to 2020
$3.8M
NICHD NIH HHS HD040307NICHD NIH HHS HD052937NICHD NIH HHS R01 HD040307NICHD NIH HHS R01 HD052937NIDDK NIH HHS P30 DK079637
6 · The paper itself

Abstract

Stem cell regulation by local signals is intensely studied, but less is known about the effects of hormonal signals on stem cells. In Drosophila, the primary steroid twenty-hydroxyecdysone (20E) regulates ovarian germline stem cells (GSCs) but was considered dispensable for testis GSC maintenance. Male GSCs reside in a microenvironment (niche) generated by somatic hub cells and adjacent cyst stem cells (CySCs). Here, we show that depletion of 20E from adult males by overexpressing a dominant negative form of the Ecdysone receptor (EcR) or its heterodimeric partner ultraspiracle (usp) causes GSC and CySC loss that is rescued by 20E feeding, uncovering a requirement for 20E in stem cell maintenance. EcR and USP are expressed, activated and autonomously required in the CySC lineage to promote CySC maintenance, as are downstream genes ftz-f1 and E75. In contrast, GSCs non-autonomously require ecdysone signaling. Global inactivation of EcR increases cell death in the testis that is rescued by expression of EcR-B2 in the CySC lineage, indicating that ecdysone signaling supports stem cell viability primarily through a specific receptor isoform. Finally, EcR genetically interacts with the NURF chromatin-remodeling complex, which we previously showed maintains CySCs. Thus, although 20E levels are lower in males than females, ecdysone signaling acts through distinct cell types and effectors to ensure both ovarian and testis stem cell maintenance.

Indexed as

AnimalsAnimals, Genetically ModifiedApoptosisCell DifferentiationCell SurvivalChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDrosophilaDrosophila ProteinsEcdysteroneEmbryonic Stem CellsFemaleGene Expression Regulation, DevelopmentalGerm CellsMaleProtein IsoformsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDrosophila ProteinsE(bx) protein, Drosophilaecdysone receptorEcdysteroneEip75B protein, Drosophilanuclear hormone receptor FTZ-F1, DrosophilaProtein IsoformsReceptors, SteroidTranscription FactorsUSP protein, DrosophilaDrosophila spermatogenesisEcdysoneNURFStem cell niche

Identifiers

PMID25093968
PMCPMC4165524
OpenAlexW2012939523

What OpenQuestion holds

Textmetadata
LicenceTDM
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.