Evidence map›Paper›PMID 30111276›Full record

ArticleBMC cell biology2018

Generation of renewable mouse intestinal epithelial cell monolayers and organoids for functional analyses.

Emily C Moorefield, R Eric Blue, Nancy L Quinney, Martina Gentzsch, Shengli Ding

Abstract read
In one paragraph

Article in BMC cell biology, 2018. 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.

  1. Review
  2. Recent advancements and limitations of intestinal organoids for clinical applications.Progress in biomedical engineering (Bristol, England) · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. In Vitro Apical-Out Enteroid Model of Necrotizing Enterocolitis.Journal of visualized experiments : JoVE · 2022
    Article
  8. Everything You Always Wanted to Know About Organoid-Based Models (and Never Dared to Ask).Cellular and molecular gastroenterology and hepatology · 2022
    Review
  9. Review
  10. Article
  11. Conditional Cell Reprogramming in Modeling Digestive System Diseases.Frontiers in cell and developmental biology · 2021
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. IFN-γ and IL-17A regulate intestinal crypt production of CXCL10 in the healthy and inflamed colon.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  18. Article
  19. Article
  20. Article
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

5 authors.

Emily C MoorefieldDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, 111 Mason Farm Road, 6340C MBRB, CB #7545, Chapel Hill, NC, 27599-7545, USA.
R Eric BlueDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, 111 Mason Farm Road, 6340C MBRB, CB #7545, Chapel Hill, NC, 27599-7545, USA.
Nancy L QuinneyMarsico Lung Institute/Cystic Fibrosis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Martina GentzschDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, 111 Mason Farm Road, 6340C MBRB, CB #7545, Chapel Hill, NC, 27599-7545, USA.
Shengli DingDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, 111 Mason Farm Road, 6340C MBRB, CB #7545, Chapel Hill, NC, 27599-7545, USA. shengli_ding@med.unc.edu.

Funding

Vector CoreP30DK065988 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Martina Gentzsch · 2004 to 2026
$26.5M
NIDDK NIH HHS P30 DK065988NIH HHS P30 DK065988
6 · The paper itself

Abstract

backgroundConditional reprogramming has enabled the development of long-lived, normal epithelial cell lines from mice and humans by in vitro culture with ROCK inhibitor on a feeder layer. We applied this technology to mouse small intestine to create 2D mouse intestinal epithelial monolayers (IEC monolayers) from genetic mouse models for functional analysis.

resultsIEC monolayers form epithelial colonies that proliferate on a feeder cell layer and are able to maintain their genotype over long-term passage. IEC monolayers form 3D spheroids in matrigel culture and monolayers on transwell inserts making them useful for functional analyses. IEC monolayers derived from the Cystic Fibrosis (CF) mouse model CFTR ∆F508 fail to respond to CFTR activator forskolin in 3D matrigel culture as measured by spheroid swelling and transwell monolayer culture via Ussing chamber electrophysiology. Tumor IEC monolayers generated from the Apc

conclusionsThese results indicate that generation of IEC monolayers is a useful model system for growing large numbers of genotype-specific mouse intestinal epithelial cells that may be used in functional studies to examine molecular mechanisms of disease and to identify and assess novel therapeutic compounds.

Indexed as

3T3 CellsAdenomatous Polyposis ColiAllelesAnimalsCell ProliferationCells, CulturedCell Self RenewalCell ShapeCellular ReprogrammingCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsIntestinal MucosaIntestinesMiceMice, Inbred C57BLCystic Fibrosis Transmembrane Conductance Regulatorcystic fibrosis transmembrane conductance regulator delta F508Intestinal epithelial cellsMonolayerMurine

Identifiers

PMID30111276
PMCPMC6094565

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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.