Evaluation of different media compositions promoting hepatocyte differentiation in the canine liver organoid model.


Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
15 Apr 2024
Historique:
received: 15 12 2023
revised: 11 03 2024
accepted: 19 03 2024
medline: 9 4 2024
pubmed: 9 4 2024
entrez: 9 4 2024
Statut: epublish

Résumé

Organoids are 3-dimensional (3D) self-assembled structures capable of replicating the microanatomy and physiology of the epithelial components of their organ of origin. Adult stem cell (ASC) derived organoids from the liver have previously been shown to differentiate into primarily mature cholangiocytes, and their partial differentiation into functional hepatocytes can be promoted using specific media compositions. While full morphological differentiation of mature hepatocytes from ASCs has not yet been reported for any species, the functional differentiation can be approximated using various media compositions. Six differentiation media formulations from published studies on hepatic organoids were used for the differentiation protocol. Target species for these protocols were humans, mice, cats, and dogs, and encompassed various combinations and concentrations of four major hepatocyte media components: Bone morphogenetic protein 7 (BMP7), Fibroblast Growth Factor 19 (FGF19), Dexamethasone (Dex), and Gamma-Secretase Inhibitor IX (DAPT). Additionally, removing R-spondin from basic organoid media has previously been shown to drive the differentiation of ASC into mature hepatocytes. Differentiation media (N = 20) were designed to encompass combinations of the four major hepatocyte media components. The preferred differentiation of ASC-derived organoids from liver tissue into mature hepatocytes over cholangiocytes was confirmed by albumin production in the culture supernatant. Out of the twenty media compositions tested, six media resulted in the production of the highest amounts of albumin in the supernatant of the organoids. The cell lines cultured using these six media were further characterized via histological staining, transmission electron microscopy, RNA

Identifiants

pubmed: 38590903
doi: 10.1016/j.heliyon.2024.e28420
pii: S2405-8440(24)04451-7
pmc: PMC10999936
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e28420

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Vojtech Gabriel (V)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Addison Lincoln (A)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Christopher Zdyrski (C)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.
3D Health Solutions Inc., Ames, IA, USA.
Precision One Health Initiative, Department of Pathology, University of Georgia College of Veterinary Medicine, 30602, Athens, GA, USA.

Abigail Ralston (A)

3D Health Solutions Inc., Ames, IA, USA.

Hannah Wickham (H)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Sydney Honold (S)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Basant H Ahmed (BH)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Karel Paukner (K)

Laboratory for Atherosclerosis Research, Institute for Clinical and Experimental Medicine, Prague, CZ, Czech Republic.

Ryan Feauto (R)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Maria M Merodio (MM)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

Pablo Piñeyro (P)

Veterinary Diagnostic Laboratory, Iowa State University, Ames, IA, USA.

David Meyerholz (D)

Department of Pathology, University of Iowa, Iowa City, IA, USA.

Karin Allenspach (K)

SMART Lab, Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.
3D Health Solutions Inc., Ames, IA, USA.
Precision One Health Initiative, Department of Pathology, University of Georgia College of Veterinary Medicine, 30602, Athens, GA, USA.

Jonathan P Mochel (JP)

3D Health Solutions Inc., Ames, IA, USA.
Precision One Health Initiative, Department of Pathology, University of Georgia College of Veterinary Medicine, 30602, Athens, GA, USA.

Classifications MeSH