Generation and Culture of Lingual Organoids Derived from Adult Mouse Taste Stem Cells

Summary

The protocol presents a method for culturing and processing lingual organoids derived from taste stem cells isolated from the posterior taste papilla of adult mice.

Abstract

The sense of taste is mediated by taste buds on the tongue, which are composed of rapidly renewing taste receptor cells (TRCs). This continual turnover is powered by local progenitor cells and renders taste function prone to disruption by a multitude of medical treatments, which in turn severely impacts the quality of life. Thus, studying this process in the context of drug treatment is vital to understanding if and how taste progenitor function and TRC production are affected. Given the ethical concerns and limited availability of human taste tissue, mouse models, which have a taste system similar to humans, are commonly used. Compared to in vivo methods, which are time-consuming, expensive, and not amenable to high throughput studies, murine lingual organoids can enable experiments to be run rapidly with many replicates and fewer mice. Here, previously published protocols have been adapted and a standardized method for generating taste organoids from taste progenitor cells isolated from the circumvallate papilla (CVP) of adult mice is presented. Taste progenitor cells in the CVP express LGR5 and can be isolated via EGFP fluorescence-activated cell sorting (FACS) from mice carrying an Lgr5^{EGFP-IRES-CreERT2} allele. Sorted cells are plated onto a matrix gel-based 3D culture system and cultured for 12 days. Organoids expand for the first 6 days of the culture period via proliferation and then enter a differentiation phase, during which they generate all three taste cell types along with non-taste epithelial cells. Organoids can be harvested upon maturation at day 12 or at any time during the growth process for RNA expression and immunohistochemical analysis. Standardizing culture methods for production of lingual organoids from adult stem cells will improve reproducibility and advance lingual organoids as a powerful drug screening tool in the fight to help patients experiencing taste dysfunction.

Introduction

In rodents, lingual taste buds are housed in fungiform papillae distributed anteriorly, bilateral foliate papillae posteriorly, as well as a single circumvallate papilla (CVP) at the posterodorsal midline of the tongue¹. Each taste bud is composed of 50-100 short-lived, rapidly renewing taste receptor cells (TRCs), which include type I glial-like support cells, type II cells that detect sweet, bitter, and umami, and type III cells that detect sour^2,3,4. In the mouse CVP, LGR5⁺ stem cells along the basal lamina produce all TRC types as well as non-taste epithelial cells⁵. When renewing the taste lineage, LGR5 daughter cells are first specified as post-mitotic taste precursor cells (type IV cells) that enter a taste bud and are capable of differentiating into any of the three TRC types⁶. The rapid turnover of TRCs renders the taste system susceptible to disruption by medical treatments, including radiation and certain drug therapies^{7,8,9,10,11,12,13}. Thus, studying the taste system in the context of taste stem cell regulation and TRC differentiation is vital for understanding how to mitigate or prevent taste dysfunction.

Mice are a traditional model for in vivo studies in taste science since they have a taste system organized similarly to humans^14,15,16. However, mice are not ideal for high throughput studies, as they are expensive to maintain and time-consuming to work with. To overcome this, in vitro organoid culture methods have been developed in recent years. Taste organoids can be generated from native CVP tissue, a process in which organoids bud off from isolated mouse CVP epithelium cultured ex vivo¹⁷. These organoids display a multilayered epithelium consistent with the in vivo taste system. A more efficient way to generate organoids that does not require ex vivo CVP culture was developed by Ren et al. in 2014¹⁸. Adapting methods and culture media first developed to grow intestinal organoids, they isolated single Lgr5-GFP⁺ progenitor cells from mouse CVP and plated them in matrix gel¹⁹. These single cells generated lingual organoids that proliferate during the first 6 days of culture, begin to differentiate around day 8, and by the end of the culture period contain non-taste epithelial cells and all three TRC types^18,20. To date, multiple studies utilizing the lingual organoid model system have been published^{17,18,20,21,22}; however, methods and culture conditions used to generate these organoids vary across publications (Supplementary Table 1). Thus, these methods have been adjusted and optimized here to present a detailed standardized protocol for the culture of lingual organoids derived from LGR5⁺ progenitors of adult mouse CVP.

Lingual organoids provide a unique model for studying the cell biological processes driving taste cell development and renewal. As the applications of lingual organoids expand and more labs move toward utilizing in vitro organoid models, it is important that the field strives to develop and adopt standardized protocols to improve reproducibility. Establishing lingual organoids as a standard tool within taste science would enable high throughput studies that tease apart how single stem cells generate the differentiated cells of the adult taste system. Additionally, lingual organoids could be employed to rapidly screen drugs for potential impacts on taste homeostasis, which could then be investigated more thoroughly in animal models. This approach ultimately will enhance efforts to devise therapies that improve the quality of life for future drug recipients.

Protocol

All the animal procedures were performed in an AAALAC-accredited facility in compliance with the Guide for the Care and Use of Laboratory Animals, Animal Welfare Act, and Public Health Service Policy, and were approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Colorado Anschutz Medical Campus. Lgr5^{EGFP-IRES-CreERT2} mice used in this protocol are from The Jackson Laboratory, Stock No. 008875.

NOTE: The following steps should be completed before beginning to ensure smooth and timely progression of the protocol: set water bath to 37 °C, set centrifuge to 4 °C, make injection and dissociation enzyme solutions from the 10 mg/mL Dispase, Collagenase, and Elastase stock solutions (see Table of Materials), remove matrix gel from -20 °C freezer (~750 µL needed for a 48-well plate) and thaw by submerging the vial in ice for at least 3-4 h, pre-coat microcentrifuge tubes in undiluted FBS by rocking gently at room temperature for at least 30 min (two 2 mL tubes for tissue collection, two 1.5 mL tubes for dissociated cells, and one 1.5 mL tube for collection of single cells from cell sorter; remove excess FBS before use).

1. Isolation of CVP epithelium

NOTE: To obtain enough LGR5⁺ cells for a full 48-well plate, collect three Lgr5-EGFP CVPs in the same tube and process simultaneously. Importantly, harvest and process the CVP of at least one wild type littermate in parallel in a separate tube and utilize it as a gating control to set FACS parameters (see Representative Results).

1. Euthanize the mice with CO₂ asphyxiation according to IACUC regulations, followed by an approved secondary method such as bilateral thoracotomy, cervical dislocation, decapitation, or exsanguination.
2. Use large sterile dissection scissors to cut the cheeks and break the jaw. Lift the tongue and cut the lingual frenulum to separate the tongue from the floor of the oral cavity. Cut out the tongue and collect it in sterile ice-cold Dulbecco's phosphate-buffered saline (dPBS) with Ca²⁺ and Mg²⁺.
3. Remove and discard the anterior tongue by cutting just anterior of the intermolar eminence with a razor blade (Figure 1A, dashed line). Use a delicate task wipe to remove any hair and excess liquid from the posterior tongue.
4. Fill 1 mL syringe with 200-300 µL of injection enzyme solution (final concentration: 2 mg/mL type-I Collagenase and 5 mg/mL Dispase II in Ca²⁺/Mg²⁺-containing dPBS, diluted from 10 mg/mL stock solutions) and insert a 30 G x ½ needle just above the intermolar eminence (Figure 1B, black arrow) until just anterior to the CVP (Figure 1B, black box). Inject the enzyme solution underneath and at the lateral edges of the CVP between the epithelium and the underlying tissues (lamina propria, muscle). Withdraw the syringe slowly and continuously from the tongue as the injection is performed.
5. Incubate the tongue in sterile Ca²⁺/Mg²⁺-free dPBS at room temperature for precisely 33 min.
6. Make small cuts in the epithelium bilaterally and just anterior to the CVP using extra fine dissection scissors, and gently peel the epithelium by lifting it with fine forceps. Once the trench epithelium is free of the underlying connective tissue, place it in an empty 2 mL microcentrifuge tube pre-coated with FBS. Do the epithelial trimming before or after detaching the CVP epithelium (Figure 1C,D).

2. Dissociation of CVP epithelium

NOTE: Dissociation of the CVP epithelium and plating are represented graphically in Figure 2.

1. Add the dissociation enzyme cocktail (final concentration: 2 mg/mL type-I Collagenase, 2 mg/mL Elastase, and 5 mg/mL Dispase II in Ca²⁺/Mg²⁺-containing dPBS, diluted from 10 mg/mL stock solutions) to tubes containing peeled CVP epithelia (200 µL per CVP). Incubate in a 37 °C water bath for 45 min. Vortex briefly every 15 min.
   NOTE: Prewarm 0.25% Trypsin-EDTA in 37 °C water bath during the last 15 min of enzyme cocktail incubation.
2. Following incubation, vortex (three pulses) then triturate with a glass Pasteur pipette for 1 min. After tissue pieces settle, pipette the supernatant containing first collection of dissociated cells, into new FBS-coated 1.5 mL microcentrifuge tubes corresponding to the genotype. Process the remaining tissue pieces further as described in step 2.3. below.
   1. Spin the supernatant for 5 min at 370 x g and 4 °C to pellet cells.
   2. Remove the resulting supernatant and resuspend the cell pellet in Fluorescence-Activated Cell Sorting (FACS) Buffer (1 mM EDTA, 25 mM HEPES (pH 7.0) and 1% FBS in Ca²⁺/Mg²⁺-free PBS (50 µL per CVP)). Store on ice.
3. While carrying out steps 2.2.1 and 2.2.2, dissociate the remaining tissue pieces from step 2.2 by adding pre-warmed 0.25% trypsin-EDTA (200 µL per CVP) to the original 2 mL microcentrifuge tubes and incubate in a 37 °C water bath for 30 min. Vortex briefly every 10 min.
4. Following incubation, vortex the tube containing tissue pieces (three pulses) then triturate with a glass Pasteur pipette for 1 min. After tissue pieces settle, pipette the supernatant into the 1.5 mL microcentrifuge tubes containing cells from step 2.2.2. Discard the tubes containing the remaining tissue pieces.
   1. Spin the tubes with dissociated cells for 5 min at 370 x g and 4 °C to pellet cells.
   2. Remove the supernatant and resuspend cell pellets in FACS Buffer (100 µL per CVP). Store on ice.
5. Pass the cells through a 30 µm nylon mesh filter and add DAPI (λ_emission = 450 nm) to cell mixtures prior to FACS. Isolate Lgr5-GFP⁺ cells via FACS using the green fluorescent protein channel (λ_excitation = 488 nm; λ_emission = 530 nm). Sort the cells using a 100 µm nozzle into a fresh FBS-coated 1.5 mL microcentrifuge tube containing 300 µL of Ca²⁺/Mg²⁺ free dPBS. Place the cells on ice until plating.

3. Plating of Lgr5-EGFP cells

1. Determine the volume of LGR5⁺ cell suspension received from the flow cytometer.
2. Based on the number of cells obtained from the sorter, calculate the number of cells per µL. Then, determine the volume needed to obtain the desired number of cells for plating (we use 200 cells per well of a 48-well plate) and transfer that total volume of suspended cells into a new microcentrifuge tube.
3. Spin the tube for 5 min at 370 x g and 4 °C to pellet cells (pellet may not be visible). Remove the supernatant and place the tube on ice.
4. Gently resuspend the cell pellet in the appropriate amount of matrix gel (15 µL per well for 48-well plates); pipette up and down gently to thoroughly distribute cells in matrix gel. Place 15 µL of matrix gel/cell mixture in the center of each well. Keep the microcentrifuge tube on ice in a 50 mL conical tube during plating to prevent matrix gel from gelling. Continue to mix matrix gel/cell mixture throughout plating by pipetting up and down every three wells to ensure an even distribution of cells across wells.
5. Place the plate in the incubator (37 °C, 5% CO₂, ~95% humidity) for 10 min to allow matrix gel gelling. Then, add 300 µL of room temperature WENRAS + Y27632 media to each well and return the plate to the incubator.

4. Organoid maintenance

NOTE: Organoids are grown in conventional organoid media (WENR) comprising recombinant EGF and 50% conditioned media containing Wnt3a, Noggin, and R-spondin²³. Drugs A8301 and SB202190 are added for the first 6 days of the culture period to optimize growth (WENRAS media) (Figure 5), then removed to promote differentiation (WENR media)²⁰. Y27632 is added for the first 2 days of culture to promote survival. Media conditions relative to the culture timeline are presented in Figure 4.

1. Two days after plating, remove WENRAS + Y27632 media from each well using a 1 mL pipette, ensuring no cross-contamination. Add 300 µL of WENRAS media down the side of the well to not disrupt the matrix gel. Return the plate to the incubator.
2. Change the media every 2 days, using the appropriate media for the culture stage (Figure 4). Maintain organoids until day 12, when the organoids are ready to harvest.

5. RNA processing

1. Harvesting organoids for RNA
   1. Place 48-well plate on ice for 30 min to depolymerize the matrix gel.
   2. Using a 1 mL pipette, pull up the organoid media; then, as the media is returned to the well, use the tip of the pipette to scratch and further break up the matrix gel. Transfer the contents to a 1.5 mL microcentrifuge tube, pooling contents of three wells in one tube. Centrifuge the tubes for 5 min at 300 x g at room temperature.
   3. Remove as much media supernatant as possible without removing any organoids; then, spin down tubes again for 5 min at 300 x g at room temperature.
   4. Remove the remaining media and resuspend the organoids in 350 µL lysis buffer + β-mercaptoethanol (βME) (10 µL βME per 1 mL lysis buffer). Place the samples on ice for immediate RNA extraction or store at -80 °C.
2. Quantitative RT-PCR analysis
   1. Measure RNA quantity via spectrophotometer. Reverse-transcribe RNA using a cDNA Synthesis Kit.
   2. Mix cDNA equivalent to 5 ng RNA with 200 nM pre-validated forward and reverse primers (Table 1) and fluorescent PCR Master Mix. Run the qRT-PCR reaction for 40 cycles at: 95 °C for 15 s, then 60 °C for 60 s.

6. Immunohistochemistry

1. Harvesting and fixing the organoids
   1. Place 48-well plate on ice for 30 min to loosen the matrix gel.
   2. Remove the organoid media and add 400 µL of ice-cold PBS to each well. Then, remove PBS and add 400 µL of ice-cold Cell Recovery Solution to each well. Rock gently at 4 °C for 30 min.
   3. Coat a 1 mL pipet tip with 1% BSA in PBS, and gently pipet contents of the well up and down to break up the matrix gel. Transfer the organoids to a 1.5 mL microcentrifuge tube placed on ice.
   4. Rinse each well with 300 µL PBS + 1% BSA and transfer any remaining organoids to the corresponding tubes. Remove Cell Recovery Solution/PBS + BSA from each tube. Add 400 µL of ice-cold PBS, then repeat with another ice-cold PBS rinse.
   5. Remove PBS and fix organoids with 300 µL ice-cold 4% PFA (in 0.1 M PB) for 20 min, incubating at room temperature. Remove PFA and rinse organoids with 400 µL ice-cold PBS.
   6. Remove PBS; then, add 400 µL PBS + 1% BSA. Store at 4 °C.
2. Immunofluorescence staining
   1. Rinse organoids in 500 µL PBS + 1% BSA. Then, incubate organoids in blocking solution (5% normal goat or donkey serum, 1% bovine serum albumin, 0.3% Triton X 100 in 1x PBS pH 7.3) for 2 h, rocking gently at room temperature.
   2. Add the primary antibody solution (primary antibodies diluted in blocking solution) and rock gently for 3 nights at 4 °C.
   3. Wash organoids 4x for 1 h with 500 µL PBS + 0.2% Triton, rocking gently at room temperature. Add secondary antibody solution (secondary antibodies diluted in blocking solution) and rock organoids overnight, protected from light, at 4 °C.
   4. Wash organoids 3x for 1 h with 500 µL PBS + 0.2% Triton, protected from light and rocking gently at room temperature. Incubate with DAPI diluted 1:10,000 in 0.1 M PB for 20 min, rocking and covered at room temperature.
   5. Wash the organoids 3x for 20 min with 0.1 M PB, rocking gently and covered at room temperature.
3. Slide mounting of organoids for inverted confocal microscopy.
   ​NOTE: Step-by-step pictures of the slide mounting process are shown in Figure 7.
   1. Create a ~1 mm thick 22 x 22 mm square perimeter of non-toxic modeling clay on a microscope slide.
   2. Remove 0.1 M PB from microcentrifuge tube, and gently resuspend organoids in 100 µL mounting medium of choice; then, transfer to center of the clay square.
   3. Fill the clay square until the mounting medium is almost to the top. Then, place 22 x 22 mm square coverslip over clay and press down firmly on the sides of the coverslip to seal. Let it cure according to the manufacturer's instructions (here, room temperature for 1-2 days) and store at 4 °C.

Results

Mice have one CVP, located posteriorly on the tongue, from which LGR5⁺ stem cells can be isolated (Figure 1A, black box). Injection of an enzyme solution under and around the CVP (Figure 1B) results in slight swelling of the epithelium and digestion of the connective tissue. Sufficient digestion is achieved following a 33 min incubation, which allows easy separation of the CVP epithelium from the underlying tissue. When attempting to ...

Discussion

Reported here is an efficient and readily repeatable method for culturing, maintaining, and processing lingual organoids derived from adult mouse taste stem cells. It was found that using three CVPs from 8 to 20-week-old Lgr5-EGFP mice is sufficient to obtain ~10,000 GFP⁺ cells for experimental use, resulting in 50 wells plated at a density of 200 cells per well in 48-well plates. Removal of CVP trench epithelia is optimized by injecting the lingual epithelium with freshly made Dispase II and type-I C...

Materials

Name	Company	Catalog Number	Comments
Antibodies
Alexa Fluor 546 Donkey anti Goat IgG	Molecular Probes	A11056, RRID: AB_142628	1:2000
Alexa Fluor 546 Goat anti Rabbit IgG	Molecular Probes	A11010, RRID:AB_2534077	1:2000
Alexa Fluor 568 Goat anti Guinea pig IgG	Invitrogen	A11075, RRID:AB_2534119	1:2000
Alexa Fluor 647 Donkey anti Rabbit IgG	Molecular Probes	A31573, RRID:AB_2536183	1:2000
Alexa Fluor 647 Goat anti Rat IgG	Molecular Probes	A21247, RRID:AB_141778	1:2000
DAPI (for FACS)	Thermo Fischer	62247
DAPI (for immunohistochemistry)	Invitrogen	D3571, RRID:AB_2307445	1:10000
Goat anti-CAR4	R&D Systems	AF2414, RRID:AB_2070332	1:50
Guinea pig anti-KRT13	Acris Antibodies	BP5076, RRID:AB_979608	1:250
Rabbit anti-GUSTDUCIN	Santa Cruz Biotechnology Inc.	sc-395, RRID:AB_673678	1:250
Rabbit anti-NTPDASE2	CHUQ	mN2-36LI6, RRID:AB_2800455	1:300
Rat anti-KRT8	DSHB	TROMA-IS, RRID: AB_531826	1:100
Equipment
2D rocker	Benchmark Scientific Inc.	BR2000
3D Rotator	Lab-Line Instruments	4630
Big-Digit Timer/Stopwatch	Fisher Scientific	S407992
Centrifuge	Eppendorf	5415D
CO2 tank	Airgas	CD USP50
FormaTM Series 3 Water Jackeed CO2 Incubator	Thermo Scientific	4110	184 L, Polished Stainless Steel
Incucyte	Sartorius	Model: S3	Cancer Center Cell Technologies Shared Resource, University of Colorado Anschutz Medical Campus
MoFlo XDP100	Cytomation Inc	Model: S13211997	Gates Center Flow Cytometry Core, University of Colorado Anschutz Medical Campus
Orbital Shaker	New Brunswick Scientific	Excella E1
Real-Time PCR System	Applied Biosystems	4376600
Refrigerated Centrifuge	Eppendorf	5417R
Spectrophotometer	Thermo Scientific	ND-1000
Stereomicroscope	Zeiss	Stemi SV6
Thermal Cycler	Bio-Rad	580BR
Vortex	Fisher Scientific	12-812
Water bath	Precision	51220073
Media
A83 01	Sigma	SML0788-5MG	Stock concentration 10 mM, final concentration 500 nM
Advanced DMEM/F12	Gibco	12634-010
B27 Supplement	Gibco	17504044	Stock concentration 50X, final concentration 1X
Gentamicin	Gibco	15750-060	Stock concentration 1000X, final concentration 1X
Glutamax	Gibco	35050061	Stock concentration 100X, final concentration 1X
HEPES	Gibco	15630080	Stock concentration 100X, final concentration 1X
Murine EGF	Peprotech	315-09-1MG	Stock concentration 500 µg/mL, final concentration 50 ng/mL
Murine Noggin	Peprotech	250-38	Stock concentration 50 µg/mL, final concentration 25 ng/mL
N-acetyl-L-cysteine	Sigma	A9165	Stock concentration 0.5 M, final concentration 1 mM
Nicotinamide	Sigma	N0636-100g	Stock concentration 1 M, final concentration 1 mM
Pen/Strep	Gibco	15140-122	Stock concentration 100X, final concentration 1X
Primocin	InvivoGen	ant-pm-1	Stock concentration 500X, final concentration 1X
SB202190	R&D Systems	1264	Stock concentration 10 mM, final concentration 0.4 µM
WRN Conditioned media			Received from Dempsey Lab (AMC Organoid and Tissue Modeling Share Resource). Derived from L-WRN (ATCC® CRL-3276™) cells
Y27632 dihydochloride 10ug	APExBIO	A3008-10	Stock concentration 10 mM, final concentration 10 µM
Other
1 ml TB Syringe	BD Syringe	309659
2-Mercaptoethanol, min. 98%	Sigma	M3148-25ML	β-mercaptoethanol
2.0 mL Microcentrifuge Tubes	USA Scientific	1420-2700
48-well plates	Thermo Scientific	150687
5 3/4 inch Pasteur Pipets	Fisherbrand	12-678-8A
Albumin from bovine serum (BSA)	Sigma Life Science	A9647-100G
Buffer RLT Lysis buffer	QIAGEN	1015750
Cell Recovery Solution	Corning	354253
Cohan-Vannas Spring Scissors	Fine Science Tools	15000-02
Collagenase from Clostridium histolyticum, type I	Sigma Life Science	C0130-1G
Cultrex RGF BME, Type 2, Pathclear	R&D Systems	3533-005-02	Matrigel
Dispase II (neutral protease, grade II)	Sigma-Aldrich (Roche)	4942078001
Disposable Filters	Sysmex	04-0042-2316
Dulbecco’s Phosphate Buffered Saline pH 7.4 (1X) (Ca2+ & Mg2+ free)	Gibco	10010-023
Dulbecco’s Phosphate Buffered Saline with Ca2+ & Mg2+	Sigma Life Sciences	D8662-500ML
Dumont #5 Forceps	Fine Science Tools	11252-30
EDTA, 0.5M (pH 8.0)	Promega	V4231
Elastase Lyophilized	Worthington Biochemical	LS002292
Extra Fine Bonn Scissors	Fine Science Tools	14084-08
Fetal Bovine Serum (FBS)	Gibco	26140-079
Fluoromount G	SouthernBiotech	0100-01
HEPES Solution	Sigma Life Science	H3537-100ML
HyClone Tryspin 0.25% + EDTA	Thermo Scientific	25200-056
iScript cDNA Synthesis Kit	Bio-Rad	1706691
Modeling Clay, Gray	Sargent Art	22-4084
Needle	BD Syringe	305106
Normal Donkey Serum	Jackson ImmunoResearch	017-000-121
Normal Goat Serum	Jackson ImmunoResearch	005-000-121
Paraformaldehyde	Sigma-Aldrich	158127
PowerSYBR Green PCR Master Mix	Applied Biosystems	4367659
RNeasy Micro Kit	QIAGEN	74004
Safe-Lock Tubes 1.5 mL	Eppendorf	022363204
Sodium Chloride	Fisher Chemical	7647-14-5
Sodium Phosphate dibasic anhydrous	Fisher Chemical	7558-79-4
Sodium Phosphate monobasic anhydrous	Fisher Bioreagents	7558-80-7
SuperFrost Plus Microscope Slides	Fisher Scientific	12-550-15
Surgical Scissors - Sharp	Fine Science Tools	14002-14
Triton X-100	Sigma Life Science	T8787-100ML
VWR micro cover glass	VWR	48366067	22x22mm