Evidence map›Paper›PMID 30837472›Full record

ArticleNature communications2019

Stem cell proliferation is induced by apoptotic bodies from dying cells during epithelial tissue maintenance.

Courtney K Brock, Stephen T Wallin, Oscar E Ruiz, Krystin M Samms, Amrita Mandal, Elizabeth A Sumner, George T Eisenhoffer

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

120 citing papers in PubMed, 176 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Bon appétit, your phagocyte.Cell death discovery · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Rewinding the clock: mechanisms of dedifferentiation.Current opinion in genetics & development · 2025
    Review
  18. Article
  19. Article
  20. Article

60 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Courtney K BrockDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Stephen T WallinDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Oscar E RuizDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Krystin M SammsDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Amrita MandalDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Elizabeth A SumnerDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
George T EisenhofferDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA. gteisenhoffer@mdanderson.org.ORCID http://orcid.org/0000-0003-0188-6782
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Regulation of Cell Turnover During Epithelial Tissue HomeostasisR01GM124043 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI EISENHOFFER, GEORGE THOMAS · 2018 to 2022
$2.0M
NCI NIH HHS P30 CA016672NIGMS NIH HHS R01 GM124043
6 · The paper itself

Abstract

Epithelial tissues require the removal and replacement of damaged cells to sustain a functional barrier. Dying cells provide instructive cues that can influence surrounding cells to proliferate, but how these signals are transmitted to their healthy neighbors to control cellular behaviors during tissue homeostasis remains poorly understood. Here we show that dying stem cells facilitate communication with adjacent stem cells by caspase-dependent production of Wnt8a-containing apoptotic bodies to drive cellular turnover in living epithelia. Basal stem cells engulf apoptotic bodies, activate Wnt signaling, and are stimulated to divide to maintain tissue-wide cell numbers. Inhibition of either cell death or Wnt signaling eliminated the apoptosis-induced cell division, while overexpression of Wnt8a signaling combined with induced cell death led to an expansion of the stem cell population. We conclude that ingestion of apoptotic bodies represents a regulatory mechanism linking death and division to maintain overall stem cell numbers and epithelial tissue homeostasis.

Indexed as

AnimalsApoptosisCaspasesCell DivisionCell ProliferationCytoskeletal ProteinsEmbryo, NonmammalianEpithelial CellsEpitheliumExtracellular Vesiclesortho-AminobenzoatesPhenylurea CompoundsSignal TransductionStem CellsWnt ProteinsZebrafishCaspasesCytoskeletal ProteinsNS3694ortho-AminobenzoatesPhenylurea Compoundswnt8a protein, zebrafishWnt ProteinsZebrafish Proteins

Identifiers

PMID30837472
PMCPMC6400930
OpenAlexW2919098257

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.