Evidence map›Paper›PMID 30188767›Full record

ArticleMolecular biology of the cell2018

Dysfunctional peroxisomes compromise gut structure and host defense by increased cell death and Tor-dependent autophagy.

Francesca Di Cara, Margret H Bülow, Andrew J Simmonds, Richard A Rachubinski

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Towards early detection of neurodegenerative diseases: A gut feeling.Frontiers in cell and developmental biology · 2023
    Review
  11. Review
  12. The Nitric Oxide Donor,Frontiers in cell and developmental biology · 2021
    Article
  13. Peroxisomes in host defense.PLoS pathogens · 2020
    Article
  14. Article
  15. Rosy Beginnings: Studying Peroxisomes inFrontiers in cell and developmental biology · 2020
    Review
  16. The Intestine ofMicroorganisms · 2019
    Review
  17. Peroxisomes and Innate Immunity: Antiviral Response and Beyond.International journal of molecular sciences · 2019
    Review
  18. Article
  19. 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 2 institutions in 2 countries.

Francesca Di CaraDepartment of Cell Biology, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Margret H BülowDevelopment, Genetics and Molecular Physiology, LIMES (Life and Medical Sciences), University of Bonn, D-53115 Bonn, Germany.
Andrew J SimmondsDepartment of Cell Biology, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Richard A RachubinskiDepartment of Cell Biology, University of Alberta, Edmonton, AB T6G 2H7, Canada.
University of Alberta · CAUniversity of Bonn · DE

Funding

CIHR
6 · The paper itself

Abstract

The gut has a central role in digestion and nutrient absorption, but it also serves in defending against pathogens, engages in mutually beneficial interactions with commensals, and is a major source of endocrine signals. Gut homeostasis is necessary for organismal health and changes to the gut are associated with conditions like obesity and diabetes and inflammatory illnesses like Crohn's disease. We report that peroxisomes, organelles involved in lipid metabolism and redox balance, are required to maintain gut epithelium homeostasis and renewal in Drosophila and for survival and development of the organism. Dysfunctional peroxisomes in gut epithelial cells activate Tor kinase-dependent autophagy that increases cell death and epithelial instability, which ultimately alter the composition of the intestinal microbiota, compromise immune pathways in the gut in response to infection, and affect organismal survival. Peroxisomes in the gut effectively function as hubs that coordinate responses from stress, metabolic, and immune signaling pathways to maintain enteric health and the functionality of the gut-microbe interface.

Indexed as

AutophagyAdenylate KinaseAnimalsCell ProliferationDrosophila melanogasterEpithelial CellsEpitheliumGastrointestinal TractHost-Pathogen InteractionsImmunityLysosomesOxidation-ReductionPeroxisomesProtein Kinase InhibitorsRegenerationSignal TransductionAdenylate KinaseProtein Kinase InhibitorsTOR Serine-Threonine Kinases

Identifiers

PMID30188767
PMCPMC6249834
OpenAlexW2889591431

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.