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This article presents a unique method for analyzing host-microbiome interactions using a novel gut organ culture system for ex vivo experiments.
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.
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 ....
This protocol follows the animal care guidelines approved by the ethics committee for animal welfare.
1. Experiment preparation
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.......
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
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.
....Name | Company | Catalog Number | Comments |
Device | |||
18 Gauge Blunt Needle | Mcmaster | 75165a754 | |
22 Gauge Blunt Needle | Mcmaster | 75165a758 | |
All Purpose Adhesive Selant 100% Silicone | DAP | 688 | |
Cubic Vacuum Desiccator VDC-21+ 2 Shelves | AAAD4021 | ||
Glass Slide 1 mm Thick | Corning | 2947-75X50 | |
Mini Incubator im-10 | AAH24315K | ||
MPC 301E Vacuum PUMP | VI-412711 | ||
Plastic Quick Turn Tube Coupling Plugs | Mcmaster | 51525k121 | |
plastic Quick Turn Tube Coupling Sockets | Mcmaster | 52525k211 | |
Sylgard 184 Silicone Elastomer | Dow | Polydimethylsiloxane, PDMS | |
Tubing | Mcmaster | 6516t11 | |
Zortrax M200 | Zortrax | Zortrax Z-SUITE, Autodesk Fusion 360 | |
Zortrax M200 Materials: z-ultrat | Zortrax | ||
Medium | |||
B27 Supplement (50x), Serum Free | Thermo Fisher Scientific | 17504044 | |
HEPES Buffer (1M) | Thermo Fisher Scientific | 15630056 | |
Iscove's Mod Dulbecco's Medium With Phenol Red (1x) | Thermo Fisher Scientific | 12440061 | |
Knock-Out Serum | Thermo Fisher Scientific | 10828028 | |
N2 Supplement (100x) | Thermo Fisher Scientific | A1370701 | |
Non Essential Amino Acid (100x) | Thermo Fisher Scientific | 11140035 | |
Surgical Tools | |||
Large Scissors | Aseltech | 11-00-10 | |
Sharp Forceps | F.S.T | 11297-10 | |
Silk Braided Surgical Thread | SMI | 8010G | |
Straight Scissors | F.S.T | 14091-09 | |
Thin Forceps | F.S.T | 11051-10 | |
Organ System | |||
0.1 µm Filter | Life Gene | ||
0.22 µm Filter | Life Gene | ||
5 mL Luer Lock Syringe | B-D | 309649 | |
Greenough Stereo Microscope | ZEISS | Stemi 305 | |
Recirculating Precision Air Heater "CUBE" | CUBE-2-LIS | ||
Syringe Pump | new era pump systems inc | nep-ne-1600-em |
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