Evidence map›Paper›PMID 24439372›Full record

ArticleCell2014

PGRP-SC2 promotes gut immune homeostasis to limit commensal dysbiosis and extend lifespan.

Linlin Guo, Jason Karpac, Susan L Tran, Heinrich Jasper

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 259 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
259citing papers in PubMed, 1 pooled it
16.3field-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

259 citing papers in PubMed, 1 synthesis or guideline pooled it, 465 citations in OpenAlex.

  1. Ageing effects of social environments in 'non-social' insects.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Pooled it
  2. A Landscape ofBiology · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. The gut as a central hub for multi-organ crosstalk in aging.Cellular and molecular life sciences : CMLS · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Gut metabolism links precision nutrition, exercise, and healthspan inbioRxiv : the preprint server for biology · 2025
    Article
  16. Article
  17. International journal of molecular sciences · 2025
    Article
  18. The Gut Microbiota ofMicroorganisms · 2025
    Review
  19. Review
  20. Article

199 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

4 authors at 3 institutions in 1 country.

Linlin GuoBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA; Department of Biomedical Genetics, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, NY 14642, USA.
Jason KarpacBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA.
Susan L TranDepartment of Biology, University of Rochester, River Campus Box 270211, Rochester, NY 14627, USA.
Heinrich JasperBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA; Department of Biology, University of Rochester, River Campus Box 270211, Rochester, NY 14627, USA. Electronic address: hjasper@buckinstitute.org.
Buck Institute for Research on Aging · USUniversity of Rochester · USUniversity of Rochester Medical Center · US

Funding

Systemic coordination of stress responses by insulin signalingR01AG028127 · NIA · UNIVERSITY OF ROCHESTER · PI JASPER, HEINRICH · 2006 to 2015
$3.0M
NIA NIH HHS R01 AG028127
6 · The paper itself

Abstract

Interactions between commensals and the host impact the metabolic and immune status of metazoans. Their deregulation is associated with age-related pathologies like chronic inflammation and cancer, especially in barrier epithelia. Maintaining a healthy commensal population by preserving innate immune homeostasis in such epithelia thus promises to promote health and longevity. Here, we show that, in the aging intestine of Drosophila, chronic activation of the transcription factor Foxo reduces expression of peptidoglycan recognition protein SC2 (PGRP-SC2), a negative regulator of IMD/Relish innate immune signaling, and homolog of the anti-inflammatory molecules PGLYRP1-4. This repression causes deregulation of Rel/NFkB activity, resulting in commensal dysbiosis, stem cell hyperproliferation, and epithelial dysplasia. Restoring PGRP-SC2 expression in enterocytes of the intestinal epithelium, in turn, prevents dysbiosis, promotes tissue homeostasis, and extends lifespan. Our results highlight the importance of commensal control for lifespan of metazoans and identify SC-class PGRPs as longevity-promoting factors.

Indexed as

Immunity, InnateModels, AnimalAnimalsCarrier ProteinsCytokinesDrosophila melanogasterDrosophila ProteinsDysbiosisForkhead Transcription FactorsHomeostasisIntestinesLongevityTranscriptomeCarrier ProteinsCytokinesDrosophila ProteinsForkhead Transcription FactorsFOXO protein, Drosophilapeptidoglycan recognition protein

Identifiers

PMID24439372
PMCPMC3928474
OpenAlexW2110628864

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.