Evidence map›Paper›PMID 34099655›Full record

ArticleNature communications2021

miR-802 regulates Paneth cell function and enterocyte differentiation in the mouse small intestine.

Algera Goga, Büsra Yagabasan, Karolin Herrmanns, Svenja Godbersen, Pamuditha N Silva, Remy Denzler, Mirjam Zünd, Markus Furter, Gerald Schwank, Shinichi Sunagawa and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Algera Goga *Institute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.
Büsra Yagabasan *Institute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-4351-6165
Karolin Herrmanns *Institute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.
Svenja GodbersenInstitute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.
Pamuditha N SilvaInstitute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.
Remy DenzlerInstitute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland.
Mirjam ZündLaboratory of Microbiome Research, Institute of Microbiology and Swiss Institute of Bioinformatics, ETH Zürich, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-2443-9328
Markus FurterInstitute of Microbiology, ETH Zurich, Zürich, Switzerland.
Gerald SchwankInstitut für Pharmakologie und Toxikologie, Universität Zürich, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-0767-2953
Shinichi SunagawaLaboratory of Microbiome Research, Institute of Microbiology and Swiss Institute of Bioinformatics, ETH Zürich, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-3065-0314
Wolf-Dietrich HardtInstitute of Microbiology, ETH Zurich, Zürich, Switzerland.ORCID http://orcid.org/0000-0002-9892-6420
Markus StoffelInstitute of Molecular Health Sciences, ETH Zurich, Zürich, Switzerland. stoffel@biol.ethz.ch.ORCID http://orcid.org/0000-0003-1304-5817
ETH Zurich · CHSIB Swiss Institute of Bioinformatics · CHUniversity of Zurich · CHJoslin Diabetes Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intestinal epithelium is a complex structure that integrates digestive, immunological, neuroendocrine, and regenerative functions. Epithelial homeostasis is maintained by a coordinated cross-talk of different epithelial cell types. Loss of integrity of the intestinal epithelium plays a key role in inflammatory diseases and gastrointestinal infection. Here we show that the intestine-enriched miR-802 is a central regulator of intestinal epithelial cell proliferation, Paneth cell function, and enterocyte differentiation. Genetic ablation of mir-802 in the small intestine of mice leads to decreased glucose uptake, impaired enterocyte differentiation, increased Paneth cell function and intestinal epithelial proliferation. These effects are mediated in part through derepression of the miR-802 target Tmed9, a modulator of Wnt and lysozyme/defensin secretion in Paneth cells, and the downstream Wnt signaling components Fzd5 and Tcf4. Mutant Tmed9 mice harboring mutations in miR-802 binding sites partially recapitulate the augmented Paneth cell function of mice lacking miR-802. Our study demonstrates a broad miR-802 network that is important for the integration of signaling pathways of different cell types controlling epithelial homeostasis in the small intestine.

Indexed as

AnimalsCell DifferentiationCell ProliferationEnterocytesFemaleFrizzled ReceptorsGene ExpressionHEK293 CellsHomeostasisHumansIntestinal MucosaIntestinesIntestine, SmallMaleMiceMice, Inbred C57BLFrizzled ReceptorsFzd5 protein, mouseMicroRNAsMIRN802 microRNA, mouseTCF4 protein, humanTranscription Factor 4Vesicular Transport Proteins

Identifiers

PMID34099655
PMCPMC8184787
OpenAlexW3167788312

What Socratic 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 Socratic graph.