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Derivation of adult canine intestinal organoids for translational research in gastroenterology.
Chandra, Lawrance; Borcherding, Dana C; Kingsbury, Dawn; Atherly, Todd; Ambrosini, Yoko M; Bourgois-Mochel, Agnes; Yuan, Wang; Kimber, Michael; Qi, Yijun; Wang, Qun; Wannemuehler, Michael; Ellinwood, N Matthew; Snella, Elizabeth; Martin, Martin; Skala, Melissa; Meyerholz, David; Estes, Mary; Fernandez-Zapico, Martin E; Jergens, Albert E; Mochel, Jonathan P; Allenspach, Karin.
Afiliação
  • Chandra L; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
  • Borcherding DC; Biomedical Sciences, Iowa State University, Ames, IA, USA.
  • Kingsbury D; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
  • Atherly T; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
  • Ambrosini YM; Biomedical Sciences, Iowa State University, Ames, IA, USA.
  • Bourgois-Mochel A; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
  • Yuan W; Biomedical Sciences, Iowa State University, Ames, IA, USA.
  • Kimber M; Biomedical Sciences, Iowa State University, Ames, IA, USA.
  • Qi Y; Departments of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA.
  • Wang Q; Departments of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA.
  • Wannemuehler M; Veterinary Microbiology and Preventative Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, USA.
  • Ellinwood NM; Animal Science, Iowa State University, Ames, IA, USA.
  • Snella E; Animal Science, Iowa State University, Ames, IA, USA.
  • Martin M; UCLA School of Medicine, Los Angeles, CA, USA.
  • Skala M; Biomedical Engineering, University of Wisconsin, Madison, WI, USA.
  • Meyerholz D; Division of Comparative Pathology, University of Iowa Carver College of Medicine, Iowa City, USA.
  • Estes M; Baylor College of Medicine, Houston, TX, USA.
  • Fernandez-Zapico ME; Schulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, MN, USA.
  • Jergens AE; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
  • Mochel JP; Biomedical Sciences, Iowa State University, Ames, IA, USA. jmochel@iastate.edu.
  • Allenspach K; Departments of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA. allek@iastate.edu.
BMC Biol ; 17(1): 33, 2019 04 11.
Article em En | MEDLINE | ID: mdl-30975131
ABSTRACT

BACKGROUND:

Large 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.

RESULTS:

Organoids 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.

CONCLUSIONS:

We 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Intestinos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Intestinos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article