Evidence map›Paper›PMID 30975131›Full record

ArticleBMC biology2019

Derivation of adult canine intestinal organoids for translational research in gastroenterology.

Lawrance Chandra, Dana C Borcherding, Dawn Kingsbury, Todd Atherly, Yoko M Ambrosini, Agnes Bourgois-Mochel, Wang Yuan, Michael Kimber, Yijun Qi, Qun Wang and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
6.6field-weighted citation impact, top 3% 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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 151 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Animal organoids as models for integrated One Health research.One health (Amsterdam, Netherlands) · 2026
    Review
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  11. Canine duodenal organoids as a functional platform for intestinal CYP regulation and drug metabolism studies.Drug metabolism and disposition: the biological fate of chemicals · 2025
    Article
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  14. Review
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18 more citing papers are in PubMed but not listed here.

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

21 authors at 6 institutions in 1 country.

Lawrance ChandraDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Dana C BorcherdingBiomedical Sciences, Iowa State University, Ames, IA, USA.
Dawn KingsburyDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Todd AtherlyDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Yoko M AmbrosiniBiomedical Sciences, Iowa State University, Ames, IA, USA.
Agnes Bourgois-MochelDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Wang YuanBiomedical Sciences, Iowa State University, Ames, IA, USA.
Michael KimberBiomedical Sciences, Iowa State University, Ames, IA, USA.
Yijun QiDepartments of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA.
Qun WangDepartments of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA.
Michael WannemuehlerVeterinary Microbiology and Preventative Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, USA.
N Matthew EllinwoodAnimal Science, Iowa State University, Ames, IA, USA.
Elizabeth SnellaAnimal Science, Iowa State University, Ames, IA, USA.
Martin MartinUCLA School of Medicine, Los Angeles, CA, USA.
Melissa SkalaBiomedical Engineering, University of Wisconsin, Madison, WI, USA.
David MeyerholzDivision of Comparative Pathology, University of Iowa Carver College of Medicine, Iowa City, USA.
Mary EstesBaylor College of Medicine, Houston, TX, USA.
Martin E Fernandez-ZapicoSchulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, MN, USA.
Albert E JergensDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Jonathan P MochelBiomedical Sciences, Iowa State University, Ames, IA, USA. jmochel@iastate.edu.
Karin AllenspachDepartments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA. allek@iastate.edu.
Iowa State University · USBaylor College of Medicine · USMayo Clinic · USUniversity of California, Los Angeles · USUniversity of Iowa · USUniversity of Wisconsin–Madison · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
Neuroimaging and Neuropathology of Mucopolysaccharidosis IR01NS085381 · NINDS · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI DICKSON, PATRICIA I · 2013 to 2017
$1.6M
6 · The paper itself

Abstract

backgroundLarge animal models, such as the dog, are increasingly being used for studying diseases including gastrointestinal (GI) disorders. Dogs share similar environmental, genomic, anatomical, and intestinal physiologic features with humans. To bridge the gap between commonly used animal models, such as rodents, and humans, and expand the translational potential of the dog model, we developed a three-dimensional (3D) canine GI organoid (enteroid and colonoid) system. Organoids have recently gained interest in translational research as this model system better recapitulates the physiological and molecular features of the tissue environment in comparison with two-dimensional cultures.

resultsOrganoids were derived from tissue of more than 40 healthy dogs and dogs with GI conditions, including inflammatory bowel disease (IBD) and intestinal carcinomas. Adult intestinal stem cells (ISC) were isolated from whole jejunal tissue as well as endoscopically obtained duodenal, ileal, and colonic biopsy samples using an optimized culture protocol. Intestinal organoids were comprehensively characterized using histology, immunohistochemistry, RNA in situ hybridization, and transmission electron microscopy, to determine the extent to which they recapitulated the in vivo tissue characteristics. Physiological relevance of the enteroid system was defined using functional assays such as optical metabolic imaging (OMI), the cystic fibrosis transmembrane conductance regulator (CFTR) function assay, and Exosome-Like Vesicles (EV) uptake assay, as a basis for wider applications of this technology in basic, preclinical and translational GI research. We have furthermore created a collection of cryopreserved organoids to facilitate future research.

conclusionsWe establish the canine GI organoid systems as a model to study naturally occurring intestinal diseases in dogs and humans, and that can be used for toxicology studies, for analysis of host-pathogen interactions, and for other translational applications.

Indexed as

AnimalsDog DiseasesDogsGastroenterologyIntestinesOrganoidsStem CellsTranslational Research, BiomedicalCanineEnteroidGI diseasesIntestinal stem cellOrganoid modelTranslational research

Identifiers

PMID30975131
PMCPMC6460554
OpenAlexW2941080670

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.