Evidence map›Paper›PMID 35479413›Full record

ArticleiScience2022

Single-cell atlas of the aging mouse colon.

Dovydas Širvinskas, Omid Omrani, Jing Lu, Mahdi Rasa, Anna Krepelova, Lisa Adam, Sandra Kaeppel, Felix Sommer, Francesco Neri

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

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  10. Regional and Sex-Dependent Immune Profiling Across the Colon in A Mouse Model of Ulcerative Colitis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 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

9 authors at 2 institutions in 1 country.

Dovydas ŠirvinskasInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Omid OmraniInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Jing LuInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Mahdi RasaInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Anna KrepelovaInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Lisa AdamInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Sandra KaeppelInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Felix SommerInstitute of Clinical Molecular Biology, Christian-Albrechts-University Kiel, 24105 Kiel, Germany.
Francesco NeriInstitute on Aging Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEChristian-Albrechts-Universität zu Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We performed massive single-cell sequencing in the aging mouse colonic epithelium and immune cells. We identified novel compartment-specific markers as well as dramatic aging-associated changes in cell composition and signaling pathways, including a shift from absorptive to secretory epithelial cells, depletion of naive lymphocytes, and induction of eIF2 signaling. Colon cancer is one of the leading causes of death within the western world, incidence of which increases with age. The colonic epithelium is a rapidly renewing tissue, tasked with water and nutrient absorption, as well as hosting intestinal microbes. The colonic submucosa is populated with immune cells interacting with and regulating the epithelial cells. However, it is unknown whether compartment-specific changes occur during aging and what impact this would cause. We show that both epithelial and immune cells differ significantly between colonic compartments and experience significant age-related changes in mice. We found a shift in the absorptive-secretory cell balance, possibly linked to age-associated intestinal disturbances, such as malabsorption. We demonstrate marked changes in aging immune cells: population shifts and interactions with epithelial cells, linking cytokines (Ifn-γ, Il1B) with the aging of colonic epithelium. Our results provide new insights into the normal and age-associated states of the colon.

Indexed as

Cell biologyImmunologyOmicsTranscriptomics

Identifiers

PMID35479413
PMCPMC9035718
OpenAlexW4224095926

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.