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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This study outlines a protocol for generating 2D monolayers of porcine organoids derived from the small and large intestines. The growth of these monolayers is marked by increasing TEER values, indicating robust epithelial integrity. Additionally, these monolayers exhibit physiological secretory responses in Ussing chamber experiments following the application of forskolin.

Abstract

The gastrointestinal tract (GIT) serves both in the digestion of food and the uptake of nutrients but also as a protective barrier against pathogens. Traditionally, research in this area has relied on animal experiments, but there's a growing demand for alternative methods that adhere to the 3R principles-replace, reduce, and refine. Porcine organoids have emerged as a promising tool, offering a more accurate in vitro replication of the in vivo conditions than traditional cell models. One major challenge with intestinal organoids is their inward-facing apical surface and outward-facing basolateral surface. This limitation can be overcome by creating two-dimensional (2D) organoid layers on transwell inserts (from here on referred to as insert(s)), providing access to both surfaces. In this study, we successfully developed two-dimensional cultures of porcine jejunum and colon organoids. The cultivation process involves two key phases: First, the formation of a cellular monolayer, followed by the differentiation of the cells using tailored media. Cellular growth is tracked by measuring transepithelial electrical resistance, which stabilizes by day 8 for colon organoids and day 16 for jejunum organoids. After a 2-day differentiation phase, the epithelium is ready for analysis. To quantify and track active electrogenic transport processes, such as chloride secretion, we employ the Ussing chamber technique. This method allows for real-time measurement and detailed characterization of epithelial transport processes. This innovative in vitro model, combined with established techniques like the Ussing chamber, provides a robust platform for physiologically characterizing the porcine GIT within the 3R framework. It also opens opportunities for investigating pathophysiological mechanisms and developing potential therapeutic strategies.

Introduction

The GIT plays a central role in digestion, nutrient absorption, and waste excretion through feces1. Additionally, it functions as a barrier against pathogens, a role supported by a diverse cellular composition, including stem cells, mucus-producing goblet cells, enteroendocrine cells, and absorptive enterocytes2. Intestinal homeostasis can be disrupted by various factors, such as bacterial infections3 or inflammatory processes4, leading to severe consequences for the organism, such as malabsorption, diarrhea, or even death5. Investigating such pathop....

Protocol

For this protocol, two healthy pigs (Bentheim Blacked Pied pig; 1 male, 1 female; 4.5 months old; approximately 65 kg) were sacrificed by captive bolt shoot and bleeding. According to the Animal Protection Law, this (slaughter and removal of tissues) is not classified as an animal experiment but has to be announced to the animal welfare officer (registration no. TiHo-T-2023-15) of the University of Veterinary Medicine Hannover Foundation.

1. Coating of inserts

NOTE: All steps are carried out with sterile materials under a safety cabinet. All steps of the protocol are performed on ice if not stated ....

Representative Results

This protocol facilitates the reliable generation of porcine 2D monolayers by disaggregating 3D organoids derived from the jejunum and colon of pigs. Over a cultivation period of 16 days for jejunum organoids and 9 days for colon organoids, intact monolayers are formed. These monolayers can subsequently be used to assess electrogenic and physiological transport properties using the Ussing chamber technique.

After disintegrating the 3D organoids, single cells are seeded onto coated inserts. Cel.......

Discussion

This protocol describes a method for converting established porcine 3D organoids into single cells, which are then seeded onto transwell membranes to form an intact monolayer. This configuration grants access to the apical side of the cells, facilitating the use of Ussing chambers to monitor absorptive and secretory processes.

The initial and crucial step in this multi-step process is the precise disintegration of the 3D organoids. Achieving uniform seeding of the single cells is essential for.......

Disclosures

We do not have any conflicts of interest to declare.

Acknowledgements

We thank the Federal Ministry of Food and Agriculture (BLE# 28N-2-071-00) for funding.

....

Materials

NameCompanyCatalog NumberComments
24 well plateSARSTEDT AG & Co. KG8,33,922
A83-01MedChemExpress, New Jersey, USAHY-10432Store at -20 °C. Thaw when needed
accujet SBrand GmbH + Co KG, Wertheim, Germany26351
Advanced DMEM/F12 MediumThermo Fisher Scientific, Waltham, USA12634010Store at 4 °C
B27 supplementThermo Fisher Scientific, Waltham, USA17504044Store at -20 °C. Thaw when needed
CaCl2.2 H2OMerck KGaA, Darmstadt, GermanyC3306Store at room temperature
D(+)-Glucose (wasserfrei)Merck KGaA, Darmstadt, Germany1.08337Store at room temperature
DAPTMedChemExpress, New Jersey, USAHY-13027Store at -20 °C. Thaw when needed
D-MannitolMerck KGaA, Darmstadt, GermanyM4125Store at room temperature
DMSOSigma-Aldrich, Schnelldorf, Germany154938Store at room temperature
Electrode-Set (AgCl/PtIr/Std.)Scientific Instruments, Simmerath, Germany#1316
Eppendorf Research plus Eppendorf SE, Hamburg, Gemany3123000063
Eppendorf Research plus Eppendorf SE, Hamburg, Gemany3123000047
EVOM3 Manual Epithelial Volt Ohm MeterWorld precision instruments, Sarasota, USAEVM-MT-03-01
FBSSigma-Aldrich, Schnelldorf, GermanyF7524Store at -20 °C. Thaw when needed
ForskolinSigma-Aldrich, Schnelldorf, GermanyF6886Store at -20 °C. Thaw when needed
gasprofi 1 SCS microWLD-TEC GmbH, Arsenhausen, Germany60,04,000
Gastrin 1MedChemExpress, New Jersey, USAHY-P1097Store at -20 °C. Thaw when needed
GlutamaxThermo Fisher Scientific, Waltham, USA35050061Store at 4 °C. 
HClSigma-Aldrich, Schnelldorf, Germany1090571000Store at room temperature
HEPESSigma-Aldrich, Schnelldorf, GermanyH0887Store at 4 °C
Herasafe 2025 Class II Biological Safety CabinetThermo Fisher Scientific, Waltham, USA51033316
Incubator ICO105Memmert GmbH + Co.KG, Schwabach, Germany62,20,143
IndomethacinMerck KGaA, Darmstadt, GermanyI7378Store at room temperature
KClMerck KGaA, Darmstadt, Germany1.04936Store at room temperature
L-GlutaminSigma-Aldrich, Schnelldorf, GermanyG7513Store at -20 °C. Thaw when needed
LWRN Supernatantselfmade Store at -20 °C. Thaw when needed. LWRN supplement is produced according to Miyoshi et al. (2012)
Matrigel Basement Membrane Matrix, LDEV-free, 10 mLCorning Incorporated - Life Sciences354234Store at -20 °C. Thaw carefully on ice when needed
Megafuge 1.ORHeraeus Instruments, Osterode, Germany75003060
MgCl2.6 H2OMerck KGaA, Darmstadt, Germany1.05833Store at room temperature
Na2HPO4.2H2OMerck KGaA, Darmstadt, Germany1.06580Store at room temperature
N-Acetyl-L-cysteineSigma-Aldrich, Schnelldorf, GermanyA7250Store at -20 °C. Thaw when needed
NaClMerck KGaA, Darmstadt, Germany1.06404Store at room temperature
NaH2PO4.H2OMerck KGaA, Darmstadt, Germany1.06346Store at room temperature
NaHCO3Merck KGaA, Darmstadt, Germany1.06329Store at room temperature
Neubauer improved chamberGlaswarenfabrik Karl Hecht, Sondheim vor der Rhön, Germany40442712
Olympus IX70 iverted MicroscopeOlympus Corporation, Hamburg, Germany
Pen/StrepThermo Fisher Scientific, Waltham, USA15140122Store at -20 °C. Thaw when needed
PolymyxinBSigma-Aldrich, Schnelldorf, GermanyP4932-1MUStore at -20 °C. Thaw when needed
Primovert microscope stand with binocular phototubeZeiss415510-1101-000
rm EGFPrepotech, New Jersey, USA315-09Store at -20 °C. Thaw when needed
SB202190MedChemExpress, New Jersey, USAHY-10295Store at -20 °C. Thaw when needed
Snapwell 3801Corning Incorporated - Life Sciences3801
Trypsin/EDTAThermo Fisher Scientific, Waltham, USA25300054
Ussing Base SystemScientific Instruments, Simmerath, Germany#1317
Ussing Diffusion ChamberScientific Instruments, Simmerath, GermanySKU 1307
Voltage/Current Clamp VCC6Scientific Instruments, Simmerath, GermanySKU 1310
Y27632MedChemExpress, New Jersey, USAHY-10583Store at -20 °C. Thaw when needed

References

  1. Hornbuckle, W. E., Tennant, B. C. . Clinical Biochemistry of Domestic Animals. , 367-406 (1997).
  2. Peterson, L. W., Artis, D. Intestinal epithelial cells: regulators of barrier function and immune homeostasis. Nat Rev Immunol. 14 (....

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