Evidence map›Paper›PMID 25633198›Full record

ArticleCell death and differentiation2015

Neural stem cell progeny regulate stem cell death in a Notch and Hox dependent manner.

R Arya, T Sarkissian, Y Tan, K White

Abstract read
In one paragraph

Article in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. The Hox Gene,Molecular biology of the cell · 2025
    Article
  3. The Hox Gene,bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Roles ofFrontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Article
  11. Genetics · 2019
    Review
  12. The Hox geneDevelopment (Cambridge, England) · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. Timing temporal transitions during brain development.Current opinion in neurobiology · 2017
    Review
  17. Review
  18. Cell death regulates muscle fiber number.Developmental biology · 2016
    Article
  19. Review
  20. Cell death in development: Signaling pathways and core mechanisms.Seminars in cell & developmental biology · 2015
    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

4 authors at 1 institution in 1 country.

R AryaCBRC, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA.
T SarkissianCBRC, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA.
Y TanCBRC, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA.
K WhiteCBRC, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA.
Massachusetts General Hospital · US

Funding

APOPTOSIS IN DROSOPHILA--FROM REAPER TO DEATHR01GM055568 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI WHITE, KRISTIN · 1997 to 2011
$3.8M
The regulation of cell death in vivoR01GM110477 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI WHITE, KRISTIN, ZHOU, LEI · 2015 to 2018
$1.4M
Nikon A1 laser scanning confocal microscope equipped for live imaging of cells anS10RR027673 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI WHITE, KRISTIN · 2010 to 2010
$500k
NCRR NIH HHS S10 RR027673NIGMS NIH HHS R01 GM055568NIGMS NIH HHS R01 GM110477NIGMS NIH HHS R01GM55568
6 · The paper itself

Abstract

Cell death is a prevalent, well-controlled and fundamental aspect of development, particularly in the nervous system. In Drosophila, specific neural stem cells are eliminated by apoptosis during embryogenesis. In the absence of apoptosis, these stem cells continue to divide, resulting in a dramatically hyperplastic central nervous system and adult lethality. Although core cell death pathways have been well described, the spatial, temporal and cell identity cues that activate the cell death machinery in specific cells are largely unknown. We identified a cis-regulatory region that controls the transcription of the cell death activators reaper, grim and sickle exclusively in neural stem cells. Using a reporter generated from this regulatory region, we found that Notch activity is required for neural stem cell death. Notch regulates the expression of the abdominalA homeobox protein, which provides important spatial cues for death. Importantly, we show that pro-apoptotic Notch signaling is activated by the Delta ligand expressed on the neighboring progeny of the stem cell. Thus we identify a previously undescribed role for progeny in regulating the proper developmental death of their parental stem cells.

Indexed as

AnimalsApoptosisCell DeathDrosophilaGene Expression Regulation, DevelopmentalNeural Stem CellsReceptors, NotchTranscription FactorsReceptors, NotchTranscription Factors

Identifiers

PMID25633198
PMCPMC4495361
OpenAlexW2029071485

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.