Evidence map›Paper›PMID 24700821›Full record

ArticleDevelopment (Cambridge, England)2014

Specification of regional intestinal stem cell identity during Drosophila metamorphosis.

Ian Driver, Benjamin Ohlstein

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Monitoring Gut Acidification in the Adult Drosophila Intestine.Journal of visualized experiments : JoVE · 2021
    Article
  7. Model systems for regeneration:Development (Cambridge, England) · 2020
    Review
  8. Article
  9. Article
  10. Intestinal renewal across the animal kingdom: comparing stem cell activity in mouse and Drosophila.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. mTOR disruption causes intestinal epithelial cell defects and intestinal atrophy postinjury in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  19. Exploring the physiology and pathology of aging in the intestine ofInvertebrate reproduction & development · 2015
    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

2 authors.

Ian DriverIntegrated Program in Cellular, Molecular and Biomedical Studies, New York, NY 10032, USA.
Benjamin Ohlstein

Funding

The Drosophila midgut: A model of human intestinal stem cells and their progeny.R01DK082456 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OHLSTEIN, BENJAMIN · 2009 to 2013
$1.6M
Stem Cells and Cell Lineage SpecificationT32HD055165 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HOBERT, OLIVER · 2007 to 2011
$1.3M
NICHD NIH HHS 5-T32-HD055165-01NICHD NIH HHS T32 HD055165NIDDK NIH HHS R01 DK082456NIDDK NIH HHS R01 DK082456-01
6 · The paper itself

Abstract

In the adult Drosophila midgut the bone morphogenetic protein (BMP) signaling pathway is required to specify and maintain the acid-secreting region of the midgut known as the copper cell region (CCR). BMP signaling is also involved in the modulation of intestinal stem cell (ISC) proliferation in response to injury. How ISCs are able to respond to the same signaling pathway in a regionally different manner is currently unknown. Here, we show that dual use of the BMP signaling pathway in the midgut is possible because BMP signals are only capable of transforming ISC and enterocyte identity during a defined window of metamorphosis. ISC heterogeneity is established prior to adulthood and then maintained in cooperation with regional signals from surrounding tissue. Our data provide a conceptual framework for how other tissues maintained by regional stem cells might be patterned and establishes the pupal and adult midgut as a novel genetic platform for identifying genes necessary for regional stem cell specification and maintenance.

Indexed as

Metamorphosis, BiologicalAgingAnimalsBone Morphogenetic ProteinsCell NucleusDrosophila melanogasterDrosophila ProteinsEnterocytesIntestinesPupaSignal TransductionStem CellsBone Morphogenetic ProteinsDrosophila ProteinsCopper cellsDrosophilaHeterogeneityIntestineStem cells

Identifiers

PMID24700821
PMCPMC3994771

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.