Generating Kidney Organoids in Suspension from Induced Pluripotent Stem Cells

Summary

This protocol presents a comprehensive and efficient method for producing kidney organoids from induced pluripotent stem cells (iPSCs) using suspension culture conditions. The primary emphasis of this study lies in the determination of the initial cell density and the WNT agonist concentration, thereby benefiting investigators interested in kidney organoid research.

Abstract

Kidney organoids can be generated from induced pluripotent stem cells (iPSCs) through various approaches. These organoids hold great promise for disease modeling, drug screening, and potential therapeutic applications. This article presents a step-by-step procedure to create kidney organoids from iPSCs, starting from the posterior primitive streak (PS) to the intermediate mesoderm (IM). The approach relies on the APEL 2 medium, which is a defined, animal component-free medium. It is supplemented with a high concentration of WNT agonist (CHIR99021) for a duration of 4 days, followed by fibroblast growth factor 9 (FGF9)/heparin and a low concentration of CHIR99021 for an additional 3 days. During this process, emphasis is given to selecting the optimal cell density and CHIR99021 concentration at the start of iPSCs, as these factors are critical for successful kidney organoid generation. An important aspect of this protocol is the suspension culture in a low adherent plate, allowing the IM to gradually develop into nephron structures, encompassing glomerular, proximal tubular, and distal tubular structures, all presented in a visually comprehensible format. Overall, this detailed protocol offers an efficient and specific technique to produce kidney organoids from diverse iPSCs, ensuring successful and consistent results.

Introduction

The kidney plays a critical role in maintaining physiological homeostasis, depending on its functional unit. Nephrons, which excrete waste products, can regulate the composition of body fluids. Chronic kidney disease (CKD), caused by hereditary mutations or other high-risk factors, will eventually progress to end-stage kidney disease (ESKD)^1,2. ESKD is apparently due to the limited regeneration capacity of nephrons. Thus, renal replacement therapy is required. Directed differentiation of human iPSCs enables the in vitro generation of patient-specific 3D kidney organoids, which can be used to study kidney development, model patient-specific diseases, and perform nephrotoxic drug screening^3,4.

During embryonic development, kidneys originate from the intermediate mesoderm (IM), which differentiates from the primitive streak (PS). The classical WNT signaling pathway may induce additional differentiation of IM with the coordinated participation of FGF (FGF9, FGF20) and BMP (Bmp7 signaling through JNK)^5,6,7. They produce two important cell populations of nephric progenitor cells (NPC): the ureteral bud (UB), and the metanephric mesenchyme (MM), forming the collecting ducts and the nephron, respectively^8,9. Each nephron consists of glomerular and tubular segments, such as the proximal and distal tubules, and the loop of Henle^10,11. According to the theory mentioned above, currently published protocols mimic the signal cascades and growth factor stimulation to induce kidney organoids^5,12.

Over the past several years, many protocols have been developed to differentiate human iPSCs into kidney organoids^5,6,7,12. Takasato et al.⁷ optimized the duration of CHIR (WNT agonist) treatment before replacement by FGF9. According to their protocol, CHIR exposure for 4 days, followed by FGF9 for 3 days, is the most effective way to induce IM from iPSCs. Transwell filters were utilized as the culture format in their procedure; however, this method is difficult for beginners. Therefore, Kumar et al.¹³ tried to change the culture format and chose to suspend the culture. They dissociated the adherent cells on Day 7 for seeding in low adherent plates to help them assemble into embryoid bodies (EBs) that contain nephron-like structures. However, the batch effect of these methods was apparent, especially in different iPSCs. Additionally, different literature reported that the concentration of CHIR varied from 7 µM to 12 µM^5,13,14.

We speculated that the concentration of cell density and the CHIR might affect the generation of organoids in different iPSCs, and this has been verified numerous times in our experiments. The present protocol has slightly modified the study method of Kumar et al.¹³ and provided users with a step-by-step procedure. The schedule and schematic of the approach are shown in Figure 1.

Protocol

The iPSCs used for the present study were obtained from a commercial source. The cells were maintained with mTeSR medium on commercially available basement membrane matrix-coated plates (see Table of Materials). Table 1 contains all the medium compositions utilized in the study.

1. Plating iPSCs for differentiation and inducing posterior primitive streak (PS)

1. Wash iPSCs on the membrane matrix-coated 6-well plate with 2 mL DPBS. Aspirate the DPBS using a pipette.
2. Add 1 mL of the commercially available cell detachment solution (see Table of Materials) to detach iPSCs and incubate at 37 °C for 5 min.
3. Add 1 mL of mTeSR to iPSCs, and ensure cells have lifted off the plastic surface.
4. Centrifuge the cells at 400 x g for 3 min at room temperature (RT). Resuspend the cell pellet and count the cell number using a hemocytometer.
5. Seed a range of cell densities onto a 24-well- or 6-well plate coated with membrane matrix and culture with mTeSR supplemented with 10 µM Rho kinase inhibitor (Y-27632) (see Table of Materials). Culture them overnight in a 37 °C CO₂ incubator.
   NOTE: To induce PS, the optimal concentration of CHIR99021 and the suitable cell densities vary from different iPSC lines. Seed a range of densities (e.g., 0.6, 0.9, 1.2, 1.5, 1.8, 2.4 * 10³ single cells per square centimeter) and a range of concentration of CHIR99021 from 7 µM-12 µM. Initiate the differentiation of each density and each CHIR on the same day. Find the optimal concentration of CHIR99021 and the suitable cell densities in a 24-well plate and then expand the culture in 6-well plates. Here we provide a protocol based on a 6-well plate.
6. Next day, aspirate the mTeSR and wash the cells with 2 mL of DPBS.
7. Add 2 mL of stage I medium (stem-cell differentiation medium containing 8-12 µM CHIR99021) (Table 1), refer to as Day 0.
8. Culture them in a 37 °C incubator for 4 days, refresh stage I medium every two days.

2. Inducing nephrogenic intermediate mesoderm (IM)

1. On Day 4, remove the stage I medium and wash with 2 mL of DPBS.
2. Add 2 mL of stage II medium to the cells (stem-cell differentiation medium containing 200 ng/mL FGF9, 1 µg/mL Heparin, and 1 µM CHIR99021) (Table 1).
3. Culture them in a 37 °C incubator, and refresh the medium every 2 days until Day 7.

3. Generating kidney organoids in suspension culture

NOTE: During the observation period from Day 0 to Day 7, the state of the cells is critical. If the cells exhibit successful expansion and heap up without significant cell debris, it demonstrates the successful derivation of the intermediate mesoderm (IM), indicating the readiness to proceed to the next stage. However, if the cells show signs of initial apoptosis, followed by necrosis or breakage, it may be indicative of inappropriate concentrations of CHIR99021 or cell densities.

1. On Day 7, remove the stage II medium and wash the cells with 2 mL of DPBS.
2. Add 1 mL of the cell detachment solution to each well and incubate at 37 °C for 5 min until cells are refractive under phase contrast.
3. Pipette 1 mL of stage II medium to cells, mix, and ensure the cells have lifted off from the surface.
4. Collect the cell suspension in a 15 mL tube and centrifuge at 400 x g for 3 min at room temperature.
5. Remove the supernatant and resuspend the cell pellet in 2 mL of stage III medium (stem-cell differentiation medium containing 200 ng/mL FGF9, 1 µg/mL Heparin, and 1 µM CHIR99021 in 0.1% Methylcellulose (MC), 0.1% Polyvinylalcohol (PVA)) supplemented with 10 µM Rho kinase inhibitor (Y-27632) (see Table of Materials). Mix it gently.
6. Mix the cell suspension and seed into a 6-well low-adhesion plate in a ratio of 1:3. Put the plate on an orbital shaker (CO₂ resistant, rotating at 60 rpm) in an incubator at 37 °C and 5% CO₂.
7. 24 h later, remove Rho kinase inhibitor (Y-27632) and add stage III media (stem-cell differentiation medium supplement with 200 ng/mL FGF9, 1 µg/mL Heparin, 1 µM CHIR99021, 0.1% MC, 0.1% PVA). Culture for 2 days. Change the medium in the suspension culture by following the steps below:
   1. Cut off the tip of the 1 mL pipette with aseptic scissors.
   2. Gently shake the 6-well plate to arrange the organoids in the middle of the plate.
   3. Aspirate the organoids with the prepared pipettes into a 15 mL tube and allow them to stand for 5 min.
   4. Aspirate the supernatant and leave the organoids at the bottom of the tube.
   5. Add the fresh medium to resuspend the organoids and replate back into a 6-well low-adhesion plate.
8. Continue shaking the low-adhesion plate at 60 rpm in the incubator. Change the stage III medium every two days until Day 12.
9. On Day 12, change the medium to stage IV medium (stem-cell differentiation medium containing 0.1% MC and 0.1% PVA).
10. Change the medium every two days until Day 25. The organoids can gradually develop into mature nephron structures from Day 12-25.

4. Immunofluorescence staining of kidney organoids

1. Collect kidney organoids into a 15 mL tube and wash with 2 mL PBS.
2. After allowing it to set for 5-10 min, fix the kidney organoids in freshly prepared 2% PFA for 20 min at 4 °C.
3. Remove the PFA and wash the organoids with 1 mL PBS containing 0.3% Triton X-100 (0.3% PBST), shake it evenly on a shaker (with a rotation speed not exceeding 60 rpm) for 8 min, allow it to stand for 5 min, and then remove the supernatant. Repeat three times.
   NOTE: The organoids can be stored in 0.3% PBST at 4° C for 2-4 weeks.
4. Incubate the fixed organoids with 10% donkey serum in PBST (blocking buffer) (see Table of Materials) overnight at 4 °C.
5. Dilute the primary antibodies (listed in the Table of Materials) in a blocking buffer with a ratio of 1:300.
6. Incubate the organoids with primary antibodies overnight at 4 °C with agitation.
   NOTE: Ensure that glomeruli and tubules can be stained simultaneously on one organoid.
7. Wash the organoids with 1 mL 0.3% PBST, shake it evenly on a shaker (with a rotation speed not exceeding 60 rpm) for 8 min, allow it to stand for 5 min, and then remove the supernatant. Repeat three times.
8. Incubate the organoids with secondary antibodies (listed in the Table of Materials) and DAPI overnight at 4 °C with agitation. Then repeat step 4.7.
   NOTE: Both secondary antibody and DAPI are diluted in blocking solution, secondary antibody (1:400) and DAPI (1:1000).
9. After the staining, dehydrate the organoids with methanol (25%, 50%, 75%, and 100% for 5 min each), then permeate with benzyl alcohol and benzyl benzoate (BABB, 1:2 ratio) (see Table of Materials) for 5 min.
10. Moute the cleared organoids on a glass-bottom dish (see Table of Materials) and examine them by confocal microscopy.
    ​NOTE: When imaging, choose the Petri dish at the bottom of the glass dish, and when permeating, put the BABB directly in the Petri dish to keep the bottom of the dish moist.

5. In vitro dextran uptake assay

1. On Day 25, incubate the organoids with 100 µg/mL of fluorescence-labeled dextran (see Table of Materials) for 4 h in an incubator at 37 °C and 5% CO₂.
2. 4 hours later, switch to a fresh medium and capture live cell culture images using a wide-field fluorescence microscope.

Results

The production of IM is achieved by activating canonical WNT signaling using the GSK3 inhibitor CHIR99021, followed by FGF9/heparin. From Day 0 to Day 4, iPSCs rapidly expand and take on rhomboid or triangular shapes. The confluence reaches 90%-100% and accumulates evenly until Day 7. Upon suspension culture, the aggregates spontaneously form nephron structures after dissociating on Day 7. The kidney organoids created through suspension culture display tubular-like structures and are easily observed in bright field image...

Discussion

A detailed protocol has been described for generating kidney organoids from iPSCs, involving minor modifications to the basal medium, initial cell density, and concentration of CHIR99021. In various experiments, the critical factors for successful kidney organoid generation were found to be the initial differentiation of the intermediate mesoderm (IM) and the cell state on Day 7. Moreover, different iPSC lines exhibited variations in cell proliferation and differentiation potential, resulting in varying optimal cell dens...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
96 Well Cell Culture Plate, Flat-Bottom	NEST	Cat #701003
Accutase	STEMCELL Technologies	Cat #07920
Antibodies
Benzyl alcohol	Sigma-Aldrich	Cat #100-51-6
Benzyl benzoate	Sigma-Aldrich	Cat #120-51-4
Biological Safety Cabinet	Haier	Cat #HR40  A2
Biotin anti-human LTL (1:300)	Vector Laboratories	Cat #B-1325
Blood mononuclear cells hiPS-B1 (iPSc, female)	N/A	N/A
Carbon dioxide level shaker	HAMANY	Cat #C0-06UC6
Chemicals, peptides, and recombinant proteins
CHIR99021 (Wnt pathway activator)	STEMCELL Technologies	Cat #72054
Costar Multiple 6 Well Cell Culture Plate	Corning	Cat #3516
Costar Ultra-Low Attachment 6 Well Plate	Corning	Cat #3471
CryoStor CS10	STEMCELL Technologies	Cat #07930
DAPI stain Solution	Coolaber	Cat #SL7102
Dextran, Alexa Fluor 647	Thermo SCIENTIFIC	Cat #D22914
DMEM/F-12 HEPES-free	Servicebio	Cat #G4610
Donkey Anti-Sheep IgG H&L (Alexa Fluor 647)	Abcam	Cat #ab150179
Donkey serum stoste	Meilunbio	Cat #MB4516-1
D-PBS (without calcium, magnesium, phenol red)	Solarbio Life Science	Cat #D1040
Dry Bath Incubator	Shanghai Jingxin	Cat #JX-10
Dylight 488-Goat Anti-Mouse IgG (1:400)	Earthox	Cat #E032210
Dylight 488-Goat Anti-Rabbit IgG (1:400)	Earthox	Cat #E032220
Dylight 549-Goat Anti-Mouse IgG (1:400)	Earthox	Cat #E032310
Dylight 549-Goat Anti-Rabbit IgG (1:400)	Earthox	Cat #E032320
Dylight 649-Goat Anti-Rabbit IgG (1:400)	Earthox	Cat #E032620
Experimental models: Cell Lines
Forma Steri-Cycle CO2 Incubator	Thermo SCIENTIFIC	Cat #370
Geltre LDEV-Free	Gibco	Cat #A1413202
Glass Bottom Culture Dishes	NEST	Cat #801002
Goat anti-human CUBN (1:300)	Santa Cruz Biotechnology	Cat #sc-20607
Heparin Solution (Cell culture supplement)	STEMCELL Technologies	Cat #07980
Human Recombinant FGF-9	STEMCELL Technologies	Cat #78161
Inverted Microscope	OLYMPUS	Cat #CKX53
Laser Scanning Confocal Microscope	OLYMPUS	Cat #FV3000
Methyl cellulose	Sigma-Aldrich	Cat #M7027
Micro Centrifuge	HENGNUO	Cat #2-4B
Mouse anti-human CD31 (1:300)	BD Biosciences	Cat #555444
Mouse anti-human ECAD (1:300)	BD Biosciences	Cat #610182
Mouse anti-human Integrin beta 1 (1:300)	Abcam	Cat #ab30394
Mouse anti-human MEIS 1/2/3 (1:300)	Thermo SCIENTIFIC	Cat #39795
Mowiol 4-88 (Polyvinylalcohol 4-88)	Sigma-Aldrich	Cat #81381
mTeSR1 5X Supplement	STEMCELL Technologies	Cat #85852
mTeSR1 Basal Medium	STEMCELL Technologies	Cat #85851
Nunc CryoTube Vials	Thermo SCIENTIFIC	Cat #377267
Others
Rabbit anti-human GATA3 (1:300)	Cell Signaling Technology	Cat #5852S
Rabbit anti-human LRP2 (1:300)	Sapphire Bioscience	Cat #NBP2-39033
Rabbit anti-human Synaptopodin (1:300)	Abcam	Cat #ab224491
Rabbit anti-human WT1 (1:300)	Abcam	Cat #ab89901
Rabbit anti-mouse PDGFR (1:300)	Abcam	Cat #ab32570
Recombinant Human Serum Albumin (rHSA)	YEASEN	Cat #20901ES03
Sheep anti-human NPHS1 (1:300)	R&D Systems	Cat #AF4269
STEMdiff APEL 2 Medium	STEMCELL Technologies	Cat #05275
Streptavidin Cy3 (1:400)	Gene Tex	Cat #GTX85902
Versene (1X)	Gibco	Cat #15040066
Y-27632 (Dihydrochloride)	STEMCELL Technologies	Cat #72304