Abstract

Simple SummaryPigs have been used in various animal model studies on the gastrointestinal tract (GIT) across both animal science and biomedical science fields. Recently, intestinal organoids have been used as a research tool for the GIT, and they have also been applied to farm animals, including pigs. However, to our knowledge, no functional studies of the porcine intestine using intestinal organoids have been conducted to date. In the present study, we developed two porcine intestinal organoid models (basal-out and apical-out organoids) and compared their characteristics. We also confirmed the possibility of conducting research related to intestinal functions, such as nutrient uptake and gut barrier function. The present study suggests that porcine intestinal organoids can be used as potential models for future GIT mechanism studies, such as host–microbe interactions, harmful ingredient tests, and nutritional research.Pig models provide valuable research information on farm animals, veterinary, and biomedical sciences. Experimental pig gut models are used in studies on physiology, nutrition, and diseases. Intestinal organoids are powerful tools for investigating intestinal functions such as nutrient uptake and gut barrier function. However, organoids have a basal-out structure and need to grow in the extracellular matrix, which causes difficulties in research on the intestinal apical membrane. We established porcine intestinal organoids from jejunum tissues and developed basal-out and apical-out organoids using different sub-culture methods. Staining and quantitative real-time PCR showed the difference in axis change of the membrane and gene expression of epithelial cell marker genes. To consider the possibility of using apical-out organoids for intestinal function, studies involving fatty acid uptake and disruption of the epithelial barrier were undertaken. Fluorescence fatty acid was more readily absorbed in apical-out organoids than in basal-out organoids within the same time. To determine whether apical-out organoids form a functional barrier, a fluorescent dextran diffusion assay was performed. Hence, we successfully developed porcine intestinal organoid culture systems and showed that the porcine apical-out organoid model is ideal for the investigation of the intestinal environment. It can be used in future studies related to the intestine across various research fields.

Highlights

  • The intestine as mucosal tissue has multiple functions, such as nutrient digestion/uptake and immune responses against external environmental agents [1]

  • The crypts were isolated by ethylenediamine-tetra acetic acid (EDTA) incubation (Figure 1B), and crypts were embedded in Matrigel in organoid culture media containing various factors for organoid development (See Material and Method Section 2.2 for organoid culture media construction)

  • In the organoid culture system, the size of each porcine crypt became larger, and the morphology changed to an intestinal organoid shape via cell proliferation and differentiation

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Summary

Introduction

The intestine as mucosal tissue has multiple functions, such as nutrient digestion/uptake and immune responses against external environmental agents [1]. The epithelium in the GIT plays functions to ensure the well-controlled regeneration of intestinal stem cells (ISCs) by forming the crypt–villus tissue architecture [3]. ISCs in the small intestine are able to differentiate into specific cell types, such as absorptive enterocytes, goblet cells, Paneth cells, and enteroendocrine cells. These intestinal epithelial cells are responsible for nutrient absorption, formation of mucus layer, production of antimicrobial peptides, and hormone secretion [4]. GIT studies using pig models that aim to understand human digestive disorders and inflammatory diseases are amongst the most appropriately applied cases compared with other organ studies [6,7,8]. There is a need to develop alternative approaches to animal experiments

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