Evidence map›Paper›PMID 23571215›Full record

ArticleDevelopment (Cambridge, England)2013

Migration of Drosophila intestinal stem cells across organ boundaries.

Shigeo Takashima, Manash Paul, Patrick Aghajanian, Amelia Younossi-Hartenstein, Volker Hartenstein

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2013. 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
1.5field-weighted citation impact, top 19% 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, 46 citations in OpenAlex.

  1. Drosophila Intestine as a Model to Study Tumors.Advances in experimental medicine and biology · 2025
    Review
  2. Paraneoplastic renal dysfunction in fly cancer models driven by inflammatory activation of stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Science advances · 2022
    Article
  6. Insect Gut Regeneration.Cold Spring Harbor perspectives in biology · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Interorgan regulation ofDevelopment (Cambridge, England) · 2017
    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

5 authors at 1 institution in 1 country.

Shigeo TakashimaDepartment of Molecular Cell and Developmental Biology, University of California-Los Angeles, CA 90095, USA.
Manash Paul
Patrick Aghajanian
Amelia Younossi-Hartenstein
Volker Hartenstein
University of California, Los Angeles · US

Funding

Genetic Control of Intestinal Stem Cells in the Drosophila HindgutR01GM087373 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HARTENSTEIN, VOLKER · 2009 to 2010
$633k
NIGMS NIH HHS [1 R01 GM087373NIGMS NIH HHS R01 GM087373
6 · The paper itself

Abstract

All components of the Drosophila intestinal tract, including the endodermal midgut and ectodermal hindgut/Malpighian tubules, maintain populations of dividing stem cells. In the midgut and hindgut, these stem cells originate from within larger populations of intestinal progenitors that proliferate during the larval stage and form the adult intestine during metamorphosis. The origin of stem cells found in the excretory Malpighian tubules ('renal stem cells') has not been established. In this paper, we investigate the migration patterns of intestinal progenitors that take place during metamorphosis. Our data demonstrate that a subset of adult midgut progenitors (AMPs) move posteriorly to form the adult ureters and, consecutively, the renal stem cells. Inhibiting cell migration by AMP-directed expression of a dominant-negative form of Rac1 protein results in the absence of stem cells in the Malpighian tubules. As the majority of the hindgut progenitor cells migrate posteriorly and differentiate into hindgut enterocytes, a group of the progenitor cells, unexpectedly, invades anteriorly into the midgut territory. Consequently, these progenitor cells differentiate into midgut enterocytes. The midgut determinant GATAe is required for the differentiation of midgut enterocytes derived from hindgut progenitors. Wingless signaling acts to balance the proportion of hindgut progenitors that differentiate as midgut versus hindgut enterocytes. Our findings indicate that a stable boundary between midgut and hindgut/Malpighian tubules is not established during early embryonic development; instead, pluripotent progenitor populations cross in between these organs in both directions, and are able to adopt the fate of the organ in which they come to reside.

Indexed as

Cell MovementAnimalsCell DifferentiationCell LineageCell ProliferationDrosophila melanogasterDrosophila ProteinsEctodermEmbryonic DevelopmentEmbryo, NonmammalianEndodermEnterocytesGATA Transcription FactorsGene Expression Regulation, DevelopmentalGenotypeIntestinal MucosaDrosophila ProteinsGATAe protein, DrosophilaGATA Transcription FactorsRac1 protein, Drosophilarac GTP-Binding Proteinswg protein, DrosophilaWnt1 Protein

Identifiers

PMID23571215
PMCPMC3631966
OpenAlexW2088413954

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.