Evidence map›Paper›PMID 32068945›Full record

ArticleCellular microbiology2020

Germ-free and microbiota-associated mice yield small intestinal epithelial organoids with equivalent and robust transcriptome/proteome expression phenotypes.

Annika Hausmann, Giancarlo Russo, Jonas Grossmann, Mirjam Zünd, Gerald Schwank, Ruedi Aebersold, Yansheng Liu, Mikael E Sellin, Wolf-Dietrich Hardt

Abstract read
In one paragraph

Article in Cellular microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

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  15. Bacterial detection by NAIP/NLRC4 elicits prompt contractions of intestinal epithelial cell layers.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  16. Review
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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.

Annika HausmannInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-8852-3444
Giancarlo RussoFunctional Genomics Center Zurich, University of Zurich, Zurich, Switzerland.
Jonas GrossmannFunctional Genomics Center Zurich, University of Zurich, Zurich, Switzerland.
Mirjam ZündInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Gerald SchwankInstitute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Ruedi AebersoldInstitute of Systems Biology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Yansheng LiuInstitute of Systems Biology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Mikael E SellinInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-8355-0803
Wolf-Dietrich HardtInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-9892-6420

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal epithelial organoids established from gut tissue have become a widely used research tool. However, it remains unclear how environmental cues, divergent microbiota composition and other sources of variation before, during and after establishment confound organoid properties, and how these properties relate to the original tissue. While environmental influences cannot be easily addressed in human organoids, mice offer a controlled assay-system. Here, we probed the effect of donor microbiota differences, previously identified as a confounding factor in murine in vivo studies, on organoids. We analysed the proteomes and transcriptomes of primary organoid cultures established from two colonised and one germ-free mouse colony of C57BL/6J genetic background, and compared them to their tissue of origin and commonly used cell lines. While an imprint of microbiota-exposure was observed on the proteome of epithelial samples, the long-term global impact of donor microbiota on organoid expression patterns was negligible. Instead, stochastic culture-to-culture differences accounted for a moderate variability between independently established organoids. Integration of transcriptome and proteome datasets revealed an organoid-typic expression signature comprising 14 transcripts and 10 proteins that distinguished organoids across all donors from murine epithelial cell lines and fibroblasts and closely mimicked expression patterns in the gut epithelium. This included the inflammasome components ASC, Naip1-6, Nlrc4 and Caspase-1, which were highly expressed in all organoids compared to the reference cell line m-IC

Indexed as

PhenotypeTranscriptomeAnimalsCell LineEpithelial CellsGene ExpressionHumansInflammasomesIntestine, SmallMaleMiceMice, Inbred C57BLMicrobiotaOrganoidsProteomeInflammasomesProteomeinflammasomemicrobiotaorganoids

Identifiers

PMID32068945
PMCPMC7317401

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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.