Evidence map›Paper›PMID 28104389›Full record

ArticleDevelopmental biology2017

Intestinal stem cell ablation reveals differential requirements for survival in response to chemical challenge.

Luís Pedro F Resende, Melissa E Truong, Adam Gomez, D Leanne Jones

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Intrinsic regulation of intestinal stem cell fate and homeostasis by Tet.bioRxiv : the preprint server for biology · 2026
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  11. Intestinal renewal across the animal kingdom: comparing stem cell activity in mouse and Drosophila.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Review
  12. Article
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  14. Review
  15. Loss ofeLife · 2017
    Article
  16. Pink1 and Parkin regulateThe Journal of cell biology · 2017
    Article
  17. 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.

Luís Pedro F ResendeDepartment of Molecular, Cell, and Developmental Biology, University of California-Los Angeles, Los Angeles, CA 90095, United States.
Melissa E TruongDepartment of Molecular, Cell, and Developmental Biology, University of California-Los Angeles, Los Angeles, CA 90095, United States.
Adam GomezDepartment of Molecular, Cell, and Developmental Biology, University of California-Los Angeles, Los Angeles, CA 90095, United States; Molecular Biology Institute, University of California-Los Angeles, Los Angeles, CA 90095, United States.
D Leanne JonesDepartment of Molecular, Cell, and Developmental Biology, University of California-Los Angeles, Los Angeles, CA 90095, United States; Molecular Biology Institute, University of California-Los Angeles, Los Angeles, CA 90095, United States; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California-Los Angeles, Los Angeles, CA 90095, United States. Electronic address: leannejones@ucla.edu.
University of California, Los Angeles · US

Funding

Characterization of Age-Related Changes in Stem Cell BehaviorR01AG028092 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE · 2007 to 2016
$3.6M
Metabolic regulation of stem cell behavior and longevityR01AG040288 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE, WALKER, DAVID W · 2012 to 2016
$3.0M
Regulation of intestinal stem cell behavior by occluding junctionsR01DK105442 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE · 2017 to 2020
$1.7M
NIA NIH HHS R01 AG028092NIA NIH HHS R01 AG040288NIDDK NIH HHS R01 DK105442
6 · The paper itself

Abstract

The Drosophila intestine is maintained by multipotent intestinal stem cells (ISCs). Although increased intestinal stem cell (ISC) proliferation has been correlated with a decrease in longevity, there is some discrepancy regarding whether a decrease or block in proliferation also has negative consequences. Here we identify headcase (hdc) as a novel marker of ISCs and enteroblasts (EBs) and demonstrate that Hdc function is required to prevent ISC/EB loss through apoptosis. Hdc depletion was used as a strategy to ablate ISCs and EBs in order to test the ability of flies to survive without ISC function. While flies lacking ISCs showed no major decrease in survival under unchallenged conditions, flies depleted of ISCs and EBs exhibited decreased survival rates in response to damage to mature enterocytes (EC) that line the intestinal lumen. Our findings indicate that constant renewal of the intestinal epithelium is not absolutely necessary under normal laboratory conditions, but it is important in the context of widespread chemical-induced damage when significant repair is necessary.

Indexed as

AnimalsApoptosisBiomarkersBleomycinCell SurvivalDrosophila melanogasterDrosophila ProteinsFemaleIntestinesRegenerationStem CellsBiomarkersBleomycinDrosophila ProteinsHdc protein, DrosophilaDrosophilaHeadcaseIntestineNicheStem cell

Identifiers

PMID28104389
PMCPMC5505510
OpenAlexW2577647246

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.