Evidence map›Paper›PMID 38335286›Full record

ArticleScience advances2024

Stem cell mTOR signaling directs region-specific cell fate decisions during intestinal nutrient adaptation.

Jaakko Mattila, Arto Viitanen, Gaia Fabris, Tetiana Strutynska, Jerome Korzelius, Ville Hietakangas

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Cytoplasmic fluidity couples nutrient availability and enterocyte fate in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

6 authors at 2 institutions in 2 countries.

Jaakko MattilaFaculty of Biological and Environmental Sciences, University of Helsinki, Helsinki 00790, Finland.ORCID 0000-0002-4064-2791
Arto ViitanenFaculty of Biological and Environmental Sciences, University of Helsinki, Helsinki 00790, Finland.ORCID 0000-0002-0197-4427
Gaia FabrisFaculty of Biological and Environmental Sciences, University of Helsinki, Helsinki 00790, Finland.ORCID 0000-0003-3453-082X
Tetiana StrutynskaFaculty of Biological and Environmental Sciences, University of Helsinki, Helsinki 00790, Finland.ORCID 0000-0003-2854-1303
Jerome KorzeliusSchool of Biosciences, University of Kent, Canterbury CT2 7NJ, UK.ORCID 0000-0002-8443-0192
Ville HietakangasFaculty of Biological and Environmental Sciences, University of Helsinki, Helsinki 00790, Finland.ORCID 0000-0002-9900-7549
University of Helsinki · FIUniversity of Kent · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The adult intestine is a regionalized organ, whose size and cellular composition are adjusted in response to nutrient status. This involves dynamic regulation of intestinal stem cell (ISC) proliferation and differentiation. How nutrient signaling controls cell fate decisions to drive regional changes in cell-type composition remains unclear. Here, we show that intestinal nutrient adaptation involves region-specific control of cell size, cell number, and differentiation. We uncovered that activation of mTOR complex 1 (mTORC1) increases ISC size in a region-specific manner. mTORC1 activity promotes Delta expression to direct cell fate toward the absorptive enteroblast lineage while inhibiting secretory enteroendocrine cell differentiation. In aged flies, the ISC mTORC1 signaling is deregulated, being constitutively high and unresponsive to diet, which can be mitigated through lifelong intermittent fasting. In conclusion, mTORC1 signaling contributes to the ISC fate decision, enabling regional control of intestinal cell differentiation in response to nutrition.

Indexed as

Intestinal MucosaIntestinesCell DifferentiationCell LineageCell ProliferationDrosophilaMechanistic Target of Rapamycin Complex 1NutrientsStem CellsTOR Serine-Threonine KinasesMechanistic Target of Rapamycin Complex 1NutrientsTOR Serine-Threonine Kinases

Identifiers

PMID38335286
PMCPMC10857434
OpenAlexW4391677406

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.