The Ex Vivo Culture and Pattern Recognition Receptor Stimulation of Mouse Intestinal Organoids

Podsumowanie

Here, a protocol to harvest, maintain, and treat mouse small intestinal organoids with pathogen associated molecular patterns (PAMPs) and Listeria monocytogenes is described, as well as emphasis on gene expression and proper normalization techniques for protein.

Streszczenie

Primary intestinal organoids are a valuable model system that has the potential to significantly impact the field of mucosal immunology. However, the complexities of the organoid growth characteristics carry significant caveats for the investigator. Specifically, the growth patterns of each individual organoid are highly variable and create a heterogeneous population of epithelial cells in culture. With such caveats, common tissue culture practices cannot be simply applied to the organoid system due to the complexity of the cellular structure. Counting and plating based solely on cell number, which is common for individually separated cells, such as cell lines, is not a reliable method for organoids unless some normalization technique is applied. Normalizing to total protein content is made complex due to the resident protein matrix. These characteristics in terms of cell number, shape and cell type should be taken into consideration when evaluating secreted contents from the organoid mass. This protocol has been generated to outline a simple procedure to culture and treat small intestinal organoids with microbial pathogens and pathogen associated molecular patterns (PAMPs). It also emphasizes the normalization techniques that should be applied when protein analysis are conducted after such a challenge.

Wprowadzenie

The ability to harvest and culture primary organoids have been described for small intestine, colon, pancreas, liver and brain and are exciting advances germane to understanding a more physiologically representative phenomena for tissue biology^1-5. The first methods describing the culture and maintenance of small intestinal organoids was reported by Sato et al. out of the lab of Hans Clevers¹. Prior to this method, harvesting and culture of primary intestinal epithelial cells proved to be limited and ineffective in sustaining epithelial cell growth. Methods included dissociation of tissue via incubation with enzymes, such as collagenase and dispase, which would ultimately lead to the outgrowth of intermixed primary fibroblast cells⁶. These conditions would also be time restricted in sustaining the epithelial cell culture. Minimal to no epithelial cell niche would form, as the epithelial cells would enter apoptosis due to the lack of appropriate growth factors or loss of contact integrity, termed anokis⁷. The advent of the 3D-organoid culture system has provided a method to culture primary intestinal cells containing a spectrum of intestinal cell types in sustained culture¹. These epithelial organoids have advantages over cell lines being that they are composed of several differentiated cells, and better mimic the organ they are derived from in vivo⁸. The process to ultimately "grow a mini gut in a dish" has proven to be a valuable tool for assessing the response of intestinal epithelium under different stimuli. Investigating the interaction of primary intestinal cells with microbial pathogen associated molecular patterns (PAMPs) is relevant to the field of immunology as these molecular patterns can regulate diverse responses from both host and microbe⁹. Not only can investigators now explore these interactions with mouse organoids, but they can be cultured from humans as well². This technology has the potential to dramatically alter personalized medicine and it is tempting to speculate about advances that this technique will make possible in the near future.

The overall goal of this method is to provide a protocol for the culture, expansion, and treatment of intestinal organoids with a variety of stimuli. Such stimuli can ultimately range from vaccines, bacterial PAMPs, live pathogens, gastrointestinal (GI) and cancer therapeutics. The isolation and culture of mouse intestinal organoids has been adapted from Sato et al. Though there are slight deviations from the original method, the end product being organoid culture is still achieved when following this protocol. This method is focused on describing an adequate technique for proper normalization when working with non-homogenous cell structures, which must be taken into consideration when conducting an assay based on cell number.

Protokół

All research was approved and conducted under Virginia Tech IACUC guidelines

1. Prepare R-Spondin1 Conditioned Media From HEK293T-Rspo1 Cell Line

1. Generation of HEK293T-Rspondin1 cells has been previously described¹⁰. Seed HEK293T-Rspondin1 secreting cells at 5-10% confluency, approximately 8 x 10⁵-1.7 x 10⁶ cells, in a T-175 flask with 40 ml of 1x Dulbecco's Modified Eagle Medium (DMEM) + 10% Fetal Bovine Serum (FBS) as the growth media, and incubate at 37 °C + 5% CO₂.  
   NOTE: The growth media for the HEK293T-Rspondin1 secreting cells will serve as R-spondin1 conditioned media. R-spondin1 can be alternatively purchased as a recombinant growth factor used at a final concentration of 500 ng/ml.
2. Grow the HEK293T-Rspondin1 cells for seven days or until reaching 95% confluency determined by bright-field microscopy. Harvest the 40 ml of conditioned media and transfer to a 50 ml conical tube. Discard the T-175 flask of HEK293T-Rspondin1 secreting cells.
3. Centrifuge the tube containing conditioned media at 300 x g for 10 min at 4 °C to pellet cellular debris. Collect the supernatant, termed R-spondin1 conditioned media, and aliquot into 15 ml tubes. Store aliquots at -20 °C for short term or -80 °C for long term storage.
   NOTE: Once thawed, the R-Spondin1 conditioned media can be stored up to 1 week a 4 °C.

2. Preparation of Organoid Growth Media and Reagents for Harvesting Small Intestinal Crypts  

1. One-day prior to harvesting, place the frozen protein matrix on ice and thaw overnight at 4 °C. Autoclave dissecting scissors, forceps and glass slides that will be used for crypt harvest.
2. The following day, begin by preparing 40 ml of organoid growth media containing supplements and growth factors by adding stock concentrations to 40 ml of 1x DMEM/F-12. Media supplements contain: 10 mM2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid (HEPES) - 400 μl, 1x glutamine supplement - 400 μl, 1x B27 without vitamin A - 400 μl, 1x N2 - 200 μl, 1 mM N-acetyl-cysteine - 40 μl, 100 ng/ml m-Noggin - 40 μl, 50 ng/ml m-EGF - 4 μl and place in a 37 ^oC water bath until usage. Warm a 15 ml aliquot of R-spondin1 to 37 °C in a water bath.
3. Warm three sterile 24 well plates to 37 °C for at least 30 min by placing in an incubator. Prepare 50 ml per mouse 1x Phosphate Buffered Saline (PBS) + 2 mM Ethylenediamine tetraacetic acid (EDTA) and cool to 4 °C. Prepare 100 ml per mouse 1x PBS containing 10% FBS and cool to 4 °C.

3. Harvesting Mus musculus Small Intestinal Crypts for Organoid Culture¹

1. Sacrifice a male C57B6/J mouse age 6-12 weeks of age raised on standard rodent chow and water available ad libitum according to institutional guidelines. Euthanize via CO₂ asphyxiation followed by cervical dislocation.
   NOTE: Keep carcass on ice until tissue harvest and perform the tissue harvest in a biological safety cabinet to minimize the risk of contamination.
   Note: A male or female mouse may be used to generate organoids.
2. (Optional) Shave the mouse to remove the fur before submersing in 70% ethanol. Submerse the mouse in 70% ethanol for 2 min and pin limbs to pinning board with the dorsal side of the mouse touching the board.
3. Use pre-sterilized dissecting scissors and forceps to make a mid-line incision on the ventral portion of the mouse. Make the incision at the genitalia proceeding cranial to the base of the neck. Open the skin incision laterally with tweezers and pin the skin to the pinning board to expose the peritoneum.
4. Make a mid-line incision in the peritoneum of the abdomen with dissecting scissors and fold the peritoneum with forceps laterally and pin to the pinning board in order to expose the abdominal organs.
   NOTE: Take care to avoid cutting abdominal organs.
5. Remove the small intestine from the abdominal cavity with dissecting forceps and scissors by cutting the proximal junction of the small intestine connected to the stomach and the distal junction connected to the caecum. Place the small intestine in a sterile petri dish containing 10 ml of ice cold 1x PBS.
6. Flush the contents contained within the lumen of the small intestine with ice cold 1x PBS using a 1 ml pipette. Repeat this step until the debris within the lumen of the small intestine is removed.
7. Cut the small intestine with dissecting scissors into 3-4 approximately equal length strips and lay the strips longitudinally on a new sterile Petri dish. For each strip, insert the cutting edge of the dissecting scissors inside the lumen of the small intestine to make an incision the entire length of the strip. Use forceps to laterally fold open the incision in order to expose the lumen of the small intestine.
8. Use a sterile glass slide to gently scrape away the villi on the luminal surface of the small intestine. Cut the small intestine into 1-2 cm length strips with dissecting scissors and transfer these strips to a 50 ml conical tube containing 10 ml ice cold 1x PBS.
9. Mix the contents gently by inverting the 50 ml conical tube and allow the tissue contents to settle to the bottom of the 50 ml conical tube. Aspirate the 1x PBS and repeat this three times by washing the tissue with 10 ml of ice cold 1x PBS. On the final wash leave the conical tube on ice for 10 min containing 10 ml 1x PBS and the small intestine tissue segments.
10. Aspirate the 1x PBS and add 25 ml of 1x PBS + 2 mM EDTA. Place on a rocking platform at 4 °C or in an ice bucket for 45 min. While the tissue is incubating, label six 15 ml conical tubes "fraction #1-6."
11. After incubation, allow the tissue contents to settle to the bottom of the tube and aspirate 1x PBS + 2 mM EDTA. Add 10 ml of 1x PBS +10% FBS and shake the tube vigorously by hand 10 times.
12. Allow the tissue contents to settle to the bottom of the tube. Remove and transfer the supernatant to the tube 15 ml conical labeled "fraction 1". Repeat the 1x PBS + 10% FBS shaking step (3.11) five times and transfer the supernatant contents in order to the appropriately labeled-fraction tube.
13. Centrifuge at 125 x g for 5 min. Aspirate the supernatant and resuspend pellets in 5 ml pre-warmed 1x DMEM/F-12, with no growth factors added.
14. Centrifuge at 78 x g for 2 min. Aspirate 4 ml of the supernatant and resuspend each pellet in 1 ml of remaining media.
15. Remove 20 ml from each fraction and add to a glass slide. Visualize crypts and debris under a light microscope and determine which fractions to combine and pool accordingly to achieve the greatest percentage of crypts to debris ratio.
    NOTE: Fractions 2-6 yield the greatest percentage of crypts to be plated. The fractions to pool are most often fraction 3 with fraction 4, and fraction 5 with fraction 6.
16. Centrifuge fractions to be plated at 125 x g for 5 min. Aspirate supernatant leaving 50-100 μl remaining above the pellet.
17. Keep tubes on ice and add 1 ml of protein matrix to the pooled fractions. Pipet up and down slowly to prevent addition of air bubbles.
18. Remove pre-warmed 24 well plates from 37 °C incubator and add 50 μl of protein matrix/crypt suspension in the middle of each well. Transfer the seeded-plate to a 37 °C incubator for 10 min to allow the protein matrix drop to solidify.
19. Add 450 μl of previously prepared organoid growth media + 50 μl of R-spondin1 conditioned media per well. Incubate plates at 37 °C + 5% CO₂ overnight.
20. Add 50-100 μl of R-spondin1 conditioned media per well daily. Every 3^rd day replace entire organoid growth media with freshly prepared organoid growth media 450 μl/well described in step 2.2. Additionally add 50-100 μl of R-spondin1 conditioned media per well.
    NOTE: The protein matrix drop maintains its integrity for one week, but after 7 days proceed to passaging organoids.

4. Passaging Organoids Every 7^th Day

1. Thaw the protein matrix on ice overnight at 4 °C the day before passaging. Warm one sterile 24 well plate to 37 °C for at least 30 min. Prepare organoid growth media described in step 2.2 and keep at 37 °C until usage.
2. Remove organoid plate from incubator and commence passaging of plate on ice. Aspirate growth media with a 10 ml pipette from 3-4 wells to start.
   NOTE: Keep the aspirated media in the 10 ml pipette, as this will be used to dislodge the protein matrix drop in the next step.
3. In the aspirated-wells, pipette up and down in order to dislodge the protein matrix drop from the plate. Gentle scraping with the tip of a 10 ml pipette is helpful in dislodging the protein matrix drop. Transfer the contents to a 15 ml conical tube.
4. Incubate the 15 ml conical tubes on ice for 10 min and centrifuge at 125 x g for 5 min at 4 °C. Observe a white pellet at the bottom of the conical tube. Gently aspirate and discard the majority of the supernatant/ old organoid growth media above the organoid pellet leaving 100-200 μl above the pellet.
5. Break up the organoid crypts by using a 23 gauge needle attached to a 1 ml syringe. Aspirate and eject 10-15 times in order to dissociate the crypts. Minimize air bubble formation due to excessive pipetting.
6. Resuspend the organoids in 500 μl of protein matrix and add 50 μl per well in a new pre-warmed 24 well plate. Add 450 μl of previously prepared organoid growth media + 50 μl of R-spondin1 conditioned media per well. Incubate plates at 37 °C overnight.

5. Plating Organoids on Day 14 for Pattern Recognition Receptor Stimulation with PAMPs and Listeria monocytogenes for Gene Expression Analysis

1. Two days prior to challenge, streak out L. monocytogenes on a BHI agar plate.
2. The following day pick a L. monocytogenes colony and grow in 10 ml of BHI broth at 37 °C overnight shaking at 200 rpm.
3. Thaw the protein matrix on ice overnight at 4 °C the day before organoid challenge. Warm one sterile 24 well plate to 37 °C for at least 30 min. Prepare organoid growth media described in step 2.2 and keep at 37 °C until usage.
4. Remove organoid culture from incubator and commence passaging of organoids.
5. Aspirate media from 3-4 wells and keep the aspirated media in the 10 ml pipete as this will be used to dislodge the protein matrix drop. Pipette up and down in order to dislodge the protein matrix drop from the plate. Gentle scraping with the tip of a 10 ml pipette is helpful in dislodging the protein matrix drop. Transfer the contents to a 15 ml conical tube.
6. Incubate the 15 ml conical tubes on ice for 10 min. Centrifuge at 125 x g for 10 min at 4 °C. Observe a white pellet at the bottom of the conical tube. Gently aspirate the supernatant leaving approximately 100 μl of residual supernatant behind.
7. Resuspend the organoid pellet in 5 ml of ice cold 1x PBS and remove a 10 μl aliquot for counting. Add the 10 μl aliquot to the middle of a hemocytometer without the glass cover slip. Gently overlay the glass coverslip on top of the drop.
   NOTE: The hemocytometer will clog with organoids if the glass slide is not first removed.
8. Count the total number of organoids via a light microscope in every grid/ the entire chamber of the hemocytometer and determine the organoid concentration: number of total organoids counted per 10 μl.
9. Remove a appropriate volume from the 15 ml conical tube that will allow adequate numbers of organoids to be seeded for the assay and centrifuge this suspension at 125 x g for 10 min.
   NOTE: The range between 40-100 organoids per well of a 24 well plate is sufficient for RNA analysis. The typical organoid size can range from 300 μm to 1,000 μm in diameter.
10. Aspirate the supernatant and resuspend the pellet in 500 ml of protein matrix without generating air bubbles. Add 50 ml of organoid/protein matrix suspension per well in a 24 well plate.  
    NOTE: The amount of protein matrix used to resuspend organoids will vary for the number of treatment conditions and technical replicates.
11. Add 500 μl of organoid growth media (without N-acetyl-cysteine) to each well and incubate at 37 °C + 5% CO₂ for 1 hr.
12. Prepare 2x concentrations of PAMPs (i.e. flagellin, lipopolysaccharide) and live L. monocytogenes. Measure the OD of live L. monocytogenes and steak on a BHI plate for counting. Treat organoids at 1 x 10⁶ Colony Forming Units (CFU)/ml.
    NOTE: The OD to CFU determination will vary by bacteria type and should be assessed prior to organoid stimulation. For example, an OD of 0.6 ≈ 1 x 10⁹ CFU/ml for L. monocytogenes, but should also be assessed independently prior to the experiment.
13. Streak out a serial dilution from the treatment stock of L. monocytogenes to accurately determine the treatment CFU/ml. The authors find that a 1 x 10⁸ dilution of 100 μl on a BHI agar plate is sufficient to count colonies to determine an accurate CFU/ml.
14. Prepare a heat killed solution of L. monocytogenes by taking a 1 ml aliquot of the live L. monocytogenes solution and centrifuge at 5,000 x g for 10 min. Aspirate the supernatant and wash the bacterial pellet with 1 ml of 1x PBS.
    1. Centrifuge the L. monocytogenes at 5,000 x g for 10 min and resuspend the pellet in 1 ml of 1x PBS. Heat kill the L. monocytogenes in a 1.7 ml polypropylene tube by heating at 80-90 °C for 1 hr. Culture a 100 μl aliquot of the heat killed L. monocytogenes on a BHI agar plate to confirm no live bacteria remain.
    2. Add 500 μl of the appropriate 2x PAMP and/or microbe treatment to 500 μl resident media in designated wells determined by the user. Incubate at 37 °C + 5% CO₂ for 24 hr.
       NOTE: Adding a 500 μl aliquot of a 2x PAMP/microbe treatment to 500 μl of resident media will bring the treatment concentration to 1x in a total volume of 1 ml.
15. The following day, manually count L. monocytogenes colonies for an accurate determination of treatment CFU/ml. Aspirate media from the plate of treated organoids and wash wells three times with 1x PBS.
16. Proceed to RNA extraction via phenol/chloroform¹¹ or a RNA extraction kit according to manufacturers instructions. Evaluate gene expression using standard qRT-PCR¹².

6. Plating Organoids on Day 14 for PAMP and L. monocytogenes Challenge for Protein Analysis in Supernatant

1. Two days prior to challenge, start a cell culture of Caco-2 cells, seeding density ≈1 x 10⁶ cells in a T-75 flask with 1x DMEM + 20% FBS and incubate the Caco-2 cells at 37 °C + 5% CO₂. Begin a bacterial culture of L. monocytogenes on BHI plate and incubate plate in a bacterial incubator at 37 °C.
2. The following day pick a L. monocytogenes colony and grow in 10 ml of BHI broth at 37 °C overnight. Thaw the protein matrix on ice overnight at 4 °C the day before organoid challenge.
3. The following day warm one sterile 96 well black-walled plate to 37 °C for at least 30 min. Prepare organoid growth media without N-acetyl-cysteine described in step 2.2 and keep at 37°C until usage. Remove organoid culture from incubator and commence passaging of organoids.
   NOTE: The typical organoid size can range from 300 μm to 1,000 μm in diameter.
4. Aspirate media from 3-4 wells and keep the aspirated media in the 10 ml pipete as this will be used to dislodge the protein matrix drop. Resuspend with a pipette in order to dislodge the protein matrix drop from plate. Gentle scraping with a 10 ml pipette is helpful in dislodging the protein matrix drop. Transfer the contents to a 15 ml conical tube.
5. Incubate the 15 ml conical tubes on ice for 10 min. Centrifuge at 125 x g for 10 min at 4 °C. Observe a white pellet at the bottom of the conical tube. Gently aspirate the supernatant leaving 100 μl of residual supernatant behind.
6. Resuspend the organoid pellet in 5ml of ice cold 1x PBS and remove a 10 μl aliquot for counting. Add the 10 μl aliquot to the middle of a hemocytometer and gently overlay the glass coverslip.
   NOTE: The hemocytometer will clog with organoids if the glass slide is not first removed.
7. Count the total number of organoids via a light microscope in every grid of the hemocytometer/ the entire chamber and determine the organoid concentration: number of total organoids counted per 10 ml.
8. Remove a appropriate volume from the 15 ml conical tube that will allow adequate numbers of organoids to be seeded for the assay and centrifuge this suspension at 125 x g for 10 min.
   NOTE: The amount of protein matrix used to resuspend organoids will vary for the amount of treatment conditions and technical replicates. The authors find that 40-100 organoids is sufficient for secreted protein analysis.
9. Aspirate the supernatant and resuspend the pellet in 500 μl of protein matrix /well without generating air bubbles.
   NOTE: The amount of protein matrix used to resuspend organoids will vary for the amount of treatment conditions and technical replicates.
10. Leave at least two columns empty on the 96 well black-walled tissue culture plate as these will serve as wells seeded with Caco-2 cells for the generation of a standard curve. Add 50 μl of protein matrix + organoid suspension per well to a pre-warmed 96 well black-walled tissue culture plate. Store the plate at 37 °C for 10 min to allow protein matrix to solidify.
11. Add 100 μl of organoid growth media (without N-acetyl-cysteine) to each well and incubate at 37 °C + 5% CO₂ for 1 hr.
12. Prepare 2x concentrations of PAMPs and live L. monocytogenes. Add 100 ml of each given treatment condition per well and incubate for 24 hr.
13. The following day plate Caco-2 cells in the standard curve wells. Begin by warming sterile 1x PBS, 0.25% trypsin and 1x DMEM + 20% FBS to 37 °C.
14. Remove the T-75 flask containing Caco-2 cells and aspirate the cell culture media. Wash the cells with 10 ml 1x PBS. Aspirate the 1x PBS, add 2 ml 0.25% Trypsin and place T-75 flask in 37 °C incubator for 15 min.
15. Visualize the flask under a light microscope to ensure the cells have detached then add 8 ml of 1x DMEM + 20% FBS to the detached Caco-2 cells and transfer into a 15 ml conical tube. Remove a 10 μl aliquot and count the cells by light microscopy using a hemocytometer.
    NOTE: An upper cell number of 60,000 cells/well works well and dilutions can be conducted for generation of the standard curve down to 2,500 cells/well.
16. Resuspend the Caco-2 cells in protein matrix and add 50 μl per well to appropriate wells. Allow the protein matrix to solidify at 37 °C for Caco-2 cells.
    NOTE: Growth media for the Caco-2 cells does not need to be added following solidification of the protein matrix.
17. Following the 24 hr treatment time for the organoid assay, aspirate and save the organoid cellular supernatant media and keep on ice. Wash the wells three times with 1x PBS. Add 100 µl of 100% methanol to each well including the Caco-2 standard curve wells and incubate at 4 °C or on ice for 20-30 min to fix the organoids.
    NOTE: It is not required that the Caco-2 standard curve wells be washed with 1x PBS, as they can have methanol added directly.
18. Following the methanol incubation, wash the wells three times with ice cold 1x PBS. Store the plate at 4 °C for up to 1-2 weeks.
19. Add nuclear staining dye at a concentration of 1 µg/ml per well, cover the plate with aluminum foil and incubate at 4 °C overnight.
20. Use a 96 well plate reader to measure nuclear staining dye excitation/emission (350nm/461nm respectively) and normalize each organoid well to the standard curve of Caco-2 cells.
21. Proceed to downstream assays, such as ELISA¹², of cell culture supernatant normalizing to cell number.

Wyniki

When following this protocol to cultivate intestinal organoids, characteristic sphere shaped organoids will be present after harvesting. The addition of R-spondin1 conditioned media daily will initiate the growth and budding of the organoids. The growth of organoids is shown in Figure 1A-F, and is representative of intestinal organoids on days 1, 2, 4, 5, 6 and day 14. Figure 1F represents the non-homogeneous growth chara...

Dyskusje

The culture and maintenance of intestinal organoids is a procedure that can be mastered by any individual with adequate tissue culture technique. There are subtleties in passaging when compared to growing cells in a more conventional monolayer, but these subtleties are not difficult to overcome. The critical steps of this method involve being able to grow the organoids to a high enough density for optimal seeding. Experiments must be scaled down with organoids as large seeding densities that can commonly be achieved with...

Materiały

Name	Company	Catalog Number	Comments
Fetal Bovine Serum (FBS)	Atlanta Biologicals	S11050	(Section 1,3,6) Or equivalent brand
Sorvall Legend XTR Centrifuge	Thermo		(Section 1,3)
DMEM	GE Healthcare	Sh30243.01	(Section 1,6) For Caco-2 and HEK293 Rspondin1 cells
HEK293T-Rspondin1 secreting cell line			(Section 1) Described and modified from Kim, K.A. et al. Lentiviral particles contained RSPO1(NM_138683) ORF cDNA cloned into a pReceiver-Lv105 backbone custom ordered and purchased from GeneCopoeia.
50 ml conical tube	Falcon	352070	(Section 1) Or equivalent brand
T-175 Flask	Corning	431079	(Section 1) Or equivalent brand
Protein Matrix	Corning	356231	(Section 2,3,4,5,6) Matrigel Growth Factor Reduced
HyClone Dulbecco's (DPBS)	GE Healthcare	SH30264.01	(Section 2,3)
DMEM/F12	Life Technologies	12634-010	(Section 2,3) Advanced DMEM/F12
Corning 24 Well TC Plates	Corning	3524	(Section 2)
N2 Supplement 100x	Life Technologies	17502-048	(Section 2)
B27 without vitamin A 50x	Life Technologies	12587-010	(Section 2)
Trizol	Life Technologies	15596-026	(Section 2)
Glutamine Supplement (Glutamax)	Life Technologies	35050-061	(Section 2) Can Combine with Advanced DMEM/ F12
HEPES (1 M)	Life Technologies	15630-080	(Section 2) Can Combine with Advanced DMEM/ F12
10ml Serological Pipet	Falcon	357551	(Section 2) Or equivalent brand
Murine Noggin	Peprotech	250-38	(Section 2) Stock = 100 mg/ml
N-Acetyl-L-cysteine	Sigma-Aldrich	A9165	(Section 2) Stock = 1M
Recombinant Mouse EGF	Biolegend	585608	(Section 2) Stock = 500 mg/ml
Rocker Variable	Bioexpres		(Section 3)
dissecting scissors			(Section 3)
forceps			(Section 3)
glass slides			(Section 3)
dissecting tweezers			(Section 3)
25 ml Serological Pipet	Falcon		(Section 3)
EDTA	Sigma-Aldrich	SLBB9821	(Section 3) 0.5M or alternative TC grade EDTA
Sterile Petri Dish 100mm x 15mm	Fisher	FB0875712	(Section 3) Or equal sized TC dish
1ml Syringe	Becton Dickinson	309659	(Section 4)
Precision Glide Needle	Becton Dickinson	305120	(Section 4) 23G x 1 1/4 (0.6mm x 30mm)
Flagellin from Bacillus subtilis	Invivogen	tlrl-bsfla	(Section 5,6)
Listeria monocytogenes	ATCC	19115	(Section 5,6) (Murray et al.)
Hemocytometer	Sigma-Aldrich	Z359629-1EA	(Section 5,6)Or equivalent brand
BBL Brain Heart Infusion Agar	Becton Dickinson	211065	(Section 5)
Bacto Brain Heart Infusion	Becton Dickinson	237500	(Section 5)
Caco-2	ATCC	HTB-37	(Section 6)
Trypsin	gibco	25200056	(section 6)
Methanol	Fisher	A412-4	(Section 6)
SpectraMax M5	Molecuar Devices		(Section 6)
96 Well Assay Plate	Corning	3603	(Section 6) Black Plate, Clear Bottom TC treated
Nuclear Staining Dye	Life Technologies	H1399	(section 6) Hoechst 33342
T-75 Flask	Corning	430641	(Section 6) Or equivalent brand
15 ml conical tube	Falcon	352096	(Section1,3) Or equivalent brand
1.7 ml polypropylene tube	Bioexpress	C-3262-1	Or equivalent brand
Quick-RNA MiniPrep	Zymo Research	R1054	Or equivalent brand
TNF-alpha	Applied Biosystems	Mm 00443260_g1	Taqman gene expression assay kit
IL-6	Applied Biosystems	(Mm 00446190_m1	Taqman gene expression assay kit
IL-1beta	Applied Biosystems	Mm 00434228_m1	Taqman gene expression assay kit
IL-18	Applied Biosystems	Mm 00434225_m1	Taqman gene expression assay kit
18s	Applied Biosystems	Hs 99999901_s1	Taqman gene expression assay kit
7500 Fast Real Time PCR System	Applied Biosystems
Nexus gradient Mastercycler	Eppendorf
TaqMan Fast Universal PCR Master Mix	Life Technologies	4352042
High Capacity cDNA Reverse Transcription Kit	Life Technologies/Applied Biosystems	4368814
Fast Optical 96-Well Reaction Plate, 0.1 mL	Life Technologies/Applied Biosystems	4346907
Recombinant Mouse R-Spondin 1 Protein	R&D Systems	3474-RS-050	500 ng/ml
chloroform	Sigma-Aldrich	C7559