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In This Article

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

Summary

This article presents a unique method for analyzing host-microbiome interactions using a novel gut organ culture system for ex vivo experiments.

Abstract

The structure of the gut tissue facilitates close and mutualistic interactions between the host and the gut microbiota. These cross-talks are crucial for maintaining local and systemic homeostasis; changes to gut microbiota composition (dysbiosis) associate with a wide array of human diseases. Methods for dissecting host-microbiota interactions encompass an inherent tradeoff among preservation of physiological tissue structure (when using in vivo animal models) and the level of control over the experiment factors (as in simple in vitro cell culture systems). To address this tradeoff, Yissachar et al. recently developed an intestinal organ culture system. The system preserves a naive colon tissue construction and cellular mechanisms and it also permits tight experimental control, facilitating experimentations that cannot be readily performed in vivo. It is optimal for dissecting short-term responses of various gut components (such as epithelial, immunological and neuronal elements) to luminal perturbations (including anaerobic or aerobic microbes, whole microbiota samples from mice or humans, drugs and metabolites). Here, we present a detailed description of an optimized protocol for organ culture of multiple gut fragments using a custom-made gut culture device. Host responses to luminal perturbations can be visualized by immunofluorescence staining of tissue sections or whole-mount tissue fragments, fluorescence in-situ hybridization (FISH), or time-lapse imaging. This system supports a wide array of readouts, including next-generation sequencing, flow cytometry, and various cellular and biochemical assays. Overall, this three-dimensional organ culture system supports the culture of large, intact intestinal tissues and has broad applications for high-resolution analysis and visualization of host-microbiota interactions in the local gut environment.

Introduction

The intestine is a highly complex organ containing a wide range of cell types (epithelial cells, immune system cells, neurons, and more) organized in a particular structure that allows cells to interact and communicate with one another and with the luminal content (microbiota, food, etc.)1. Currently, the research toolbox available for analyzing host-microbiota interactions includes in vitro cell cultures and in vivo animal models2. In vivo animal models provide a physiological tissue construction3 but with poor experimental control and limited ability to manipulate the ....

Protocol

This protocol follows the animal care guidelines approved by the ethics committee for animal welfare.

1. Experiment preparation

  1. Fabrication of the gut organ culture device (3 days)
    1. Using a 3D printer, print the reusable plastic molds for the organ culture device (the device has 6 wells, with 24 small and large holes, and for the device cover lid) (3D files attached).
      NOTE: These plastic molds may be used for fabrication of numerous devices.
    2. Insert the.......

Representative Results

The gut organ culture system maintains tissue viability ex vivo. The evaluation of the tissue viability was done throughout the culture period. Colon tissue fragments were incubated in the gut organ culture system and fixed following 2/12/24 h culture. The intestinal epithelial cell (IEC) layer integrity was validated by immunofluorescence staining using E-cadherin and cytokeratin-18 antibodies. Likewise, mucus-filled goblet cells in the colonic epithelium and mucus secretion within the lumen were detected as we.......

Discussion

This article describe an optimized protocol for ex vivo gut organ cultures that Yissachar et al. have recently developed (published9 and unpublished data). The gut organ culture system supports multiplexed culture of intact intestinal fragments while maintaining luminal flow. It provides full control over the intra- and extra-luminal environment (including stimulation dose, exposure time and flow rate) and preserves the naïve intestinal tissue structure and its cellular complexity

Acknowledgements

We thank past and present members of the Yissachar lab for their valuable contributions in optimizing the gut organ culture system protocol. We thank Yael Laure for critical editing of the manuscript. This work was supported by the Israel Science Foundation (grant No. 3114831), the Israel Science Foundation - Broad Institute Joint Program (grant No. 8165162), and the Gassner Fund for Medical Research, Israel.

....

Materials

NameCompanyCatalog NumberComments
Device
18 Gauge Blunt NeedleMcmaster75165a754
22 Gauge Blunt NeedleMcmaster75165a758
All Purpose Adhesive Selant 100% SiliconeDAP688
Cubic Vacuum Desiccator VDC-21+ 2 ShelvesAAAD4021
Glass Slide 1 mm ThickCorning2947-75X50
Mini Incubator im-10AAH24315K
MPC 301E Vacuum PUMPVI-412711
Plastic Quick Turn Tube Coupling PlugsMcmaster51525k121
plastic Quick Turn Tube Coupling SocketsMcmaster52525k211
Sylgard 184 Silicone ElastomerDowPolydimethylsiloxane, PDMS
TubingMcmaster6516t11
Zortrax M200ZortraxZortrax Z-SUITE, Autodesk Fusion 360
Zortrax M200 Materials: z-ultratZortrax
Medium
B27 Supplement (50x), Serum FreeThermo Fisher Scientific17504044
HEPES Buffer (1M)Thermo Fisher Scientific15630056
Iscove's Mod Dulbecco's Medium With Phenol Red (1x)Thermo Fisher Scientific12440061
Knock-Out SerumThermo Fisher Scientific10828028
N2 Supplement (100x)Thermo Fisher ScientificA1370701
Non Essential Amino Acid (100x)Thermo Fisher Scientific11140035
Surgical Tools
Large ScissorsAseltech11-00-10
Sharp ForcepsF.S.T11297-10
Silk Braided Surgical ThreadSMI8010G
Straight ScissorsF.S.T14091-09
Thin ForcepsF.S.T11051-10
Organ System
0.1 µm FilterLife Gene
0.22 µm FilterLife Gene
5 mL Luer Lock SyringeB-D309649
Greenough Stereo MicroscopeZEISSStemi 305
Recirculating Precision Air Heater "CUBE"CUBE-2-LIS
Syringe Pumpnew era pump systems incnep-ne-1600-em

References

  1. Mowat, A. M., Agace, W. W. Regional specialization within the intestinal immune system. Nature Reviews Immunology. 14 (10), 667-685 (2014).
  2. Pearce, S. C., et al. Intestinal in vitro and ex vivo Mo....

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