Evidence map›Paper›PMID 23010510›Full record

ArticleDevelopmental biology2012

Jak-STAT regulation of cyst stem cell development in the Drosophila testis.

D Sinden, M Badgett, J Fry, T Jones, R Palmen, X Sheng, A Simmons, E Matunis, M Wawersik

Abstract read
In one paragraph

Article in Developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Lin28 Represses Hub Cell microRNAs to MaintainDevelopment & reproduction · 2026
    Review
  2. Metabolic Regulation in the Maintenance ofInternational journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. JAK/STAT signaling in stem cells and regeneration: fromDevelopment (Cambridge, England) · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

9 authors at 2 institutions in 1 country.

D SindenCollege of William & Mary, Biology Department, Williamsburg, VA 23185, USA.
M Badgett
J Fry
T Jones
R Palmen
X Sheng
A Simmons
E Matunis
M Wawersik
William & Mary · USJohns Hopkins University · US

Funding

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
Request for Zeiss LSM 510 MP Multiphoton Imaging SystemS10RR024550 · NCRR · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2008 to 2008
$500k
Howard Hughes Medical InstituteNCRR NIH HHS S10 RR024550NICHD NIH HHS R01 HD040307NICHD NIH HHS R01HD040307NICHD NIH HHS R01 HD052937
6 · The paper itself

Abstract

Establishment and maintenance of functional stem cells is critical for organ development and tissue homeostasis. Little is known about the mechanisms underlying stem establishment during organogenesis. Drosophila testes are among the most thoroughly characterized systems for studying stem cell behavior, with germline stem cells (GSCs) and somatic cyst stem cells (CySCs) cohabiting a discrete stem cell niche at the testis apex. GSCs and CySCs are arrayed around hub cells that also comprise the niche and communication between hub cells, GSCs, and CySCs regulates the balance between stem cell maintenance and differentiation. Recent data has shown that functional, asymmetrically dividing GSCs are first established at ∼23 h after egg laying during Drosophila testis morphogenesis (Sheng et al., 2009). This process correlates with coalescence of the hub, but development of CySCs from somatic gonadal precursors (SGPs) was not examined. Here, we show that functional CySCs are present at the time of GSC establishment, and that Jak-STAT signaling is necessary and sufficient for CySC maintenance shortly thereafter. Furthermore, hyper-activation of Jak in CySCs promotes expansion of the GSC population, while ectopic Jak activation in the germline induces GSC gene expression in GSC daughter cells but does not prevent spermatogenic differentiation. Together, these observations indicate that, similar to adult testes, Jak-STAT signaling from the hub acts on both GSCs and CySC to regulate their development and differentiation, and that additional signaling from CySCs to the GSCs play a dominant role in controlling GSC maintenance during niche formation.

Indexed as

Cell DifferentiationAnimalsDrosophilaDrosophila ProteinsEmbryo, NonmammalianGerm CellsJanus KinasesMaleModels, BiologicalMorphogenesisSignal TransductionSTAT Transcription FactorsStem Cell NicheStem CellsTestisTranscription FactorsDrosophila Proteinshop protein, DrosophilaJanus KinasesSTAT Transcription FactorsTranscription Factors

Identifiers

PMID23010510
PMCPMC3481170
OpenAlexW2059368499

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.