Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Podsumowanie

This protocol describes the generation of integration free iPSCs from fetal tissue fibroblasts through delivery of episomal plasmids by nucleofection followed by description of methods used for iPSC characterization and neuronal differentiation.

Streszczenie

Chromosomal aneuploidies cause severe congenital malformations including central nervous system malformations and fetal death. Prenatal genetic screening is purely diagnostic and does not elucidate disease mechanism. Although cells from aneuploid fetuses are valuable biological material bearing the chromosomal aneuploidy, these cells are short lived, limiting their use for downstream research experiments. Generation of induced pluripotent stem cell (iPSC) models is an effective method of cell preparation for perpetual conservation of aneuploid traits. They are self-renewing and differentiate into specialized cells reminiscent of embryonic development. Thus, iPSCs serve as excellent tools to study early developmental events. Turner syndrome (TS) is a rare condition associated with a completely or partially missing X chromosome. The syndrome is characterized by infertility, short stature, endocrine, metabolic, autoimmune and cardiovascular disorders and neurocognitive defects. The following protocol describes isolation and culturing of fibroblasts from TS (45XO) fetal tissue, generation of integration free TSiPSCs through delivery of episomal reprogramming plasmids by nucleofection followed by characterization. The reprogramming TSiPSCs were initially screened by live cell alkaline phosphatase staining followed by extensive probing for pluripotency biomarkers. Selected colonies were mechanically dissected, passaged several times and stable self-renewing cells were used for further experiments. The cells expressed pluripotency transcription factors OCT4, NANOG, SOX2, cell surface markers SSEA 4 and TRA1-81 typical of pluripotent stem cells. The original 45XO karyotype was retained post reprogramming. The TSiPSCs were able to form embryoid bodies and differentiate into cells of endoderm, mesoderm and ectoderm expressing lineage specific biomarkers ((SRY BOX17), (MYOSIN VENTRICULAR HEAVY CHAINα/β), (βIII TUBULIN)). The exogenous episomal plasmids were lost spontaneously and not detected after passage 15 in cells. These TSiPSCs are a valuable cellular resource for modelling defective molecular and cellular neurodevelopment causing neurocognitive deficits associated with Turner syndrome.

Wprowadzenie

Aneuploidies lead to birth defects/congenital malformations and pregnancy loss in humans. ~50%-70% of specimens from pregnancy losses show cytogenetic abnormalities. Aneuploid embryos lost early in pregnancy cannot be easily obtained for experimental analysis raising the need to develop other models closely representing human embryogenesis. Induced pluripotent stem cells (iPSCs) derived from cells diagnosed with genetic disorders have been used to model the representative genetic irregularities and their consequence on fetal development^1,2,3,4. These iPSCs resemble epiblast cells of the developing embryo and can recapitulate the early events of embryo formation. They allow understanding and characterization of the developmental program of cell lineages and patterning in early mammalian embryos. iPSCs derived previously from skin fibroblasts and amniocytes from prenatal diagnostic tests of aneuploidy syndromes like monosomy X (Turner syndrome), trisomy 8 (Warkany syndrome 2), trisomy 13 (Patau syndrome) and partial trisomy 11; 22 (Emanuel syndrome) have provided valuable insights regarding failed development⁴.

Turner syndrome (TS) is a rare condition characterized by female infertility, short stature, endocrine and metabolic disorders, an increased risk of autoimmune disease, and a predisposition to cardiovascular disease⁵. Though it is the only survivable monosomy syndrome it is also lethal to the developing embryo causing spontaneous abortions⁶. Surviving individuals with TS present with degrees of alteration of X-chromosomal material in their cells. Karyotypes range from complete loss of one X chromosome (45,XO) to mosaics like 45,XO/46,XX; 45,XO/47,XXX, the presence of ring chromosomes, the presence of Y-chromosomal material, etc⁵.

Diagnosis of the syndrome is generally done by karyotyping blood of symptomatic individuals and chorionic villi sampling (CVS) to detect early aneuploidy syndromes. Since aneuploidy syndromes account for ~30% of spontaneous abortions, it is routine to karyotype the product of conception (POC) upon a spontaneous abortion. These fetal cells including the chorionic villi possessing the cytogenetic abnormality and iPSCs derived from them provide a valuable source of biological material to study aneuploidy syndromes^4,6. TS iPSCs have been previously established from amniocytes via retroviral reprogramming⁴, fibroblasts of chorionic villi (obtained through prenatal diagnosis) via retroviral reprogramming⁶, from blood mononuclear cells⁷ via Sendai virus reprogramming and from skin fibroblasts of TS individuals via lentiviral reprogramming⁴. Since the primary focus of our lab is to understand developmental failure, we have generated TS iPSCs from POC, specifically the chorionic villi component of a spontaneous abortion⁸. All the cells isolated from this fetal tissue had a 45XO karyotype and yielded iPSCs with the same karyotype. These iPSCs are unique as they are the first to be generated from an aborted fetus and provide a valuable resource to study aneuploidy related pregnancy failures. This article provides a detailed methodology of the generation of iPSCs from this unique cell source via episomal reprogramming.

The early methods of iPSC generation used viral transduction and transposons to deliver the reprogramming factors. Methods of inducing cells to pluripotency have evolved from using integrating retroviral vectors⁹, excisable lentiviral vectors^10,11 and transposon-based methods¹² to non-integrating adenoviral vectors¹³ and Sendai virus based vectors¹⁴. Retroviral and lentiviral based reprogramming, although efficient, involve integration of the reprogramming factors into the host chromosomes, causing insertion mutations which have unforeseen effects in the iPSCs. Furthermore, viral-based reprogramming prevents translational application of iPSCs. RNA-based systems¹⁵ and direct protein delivery¹⁶ have been explored to completely eliminate the potential risks associated with the use of viruses and DNA transfections. However, these methods have proven inefficient.

In 2011, Okita et al. reported improved efficiency of reprogramming by episomal plasmids augmented with TP53 suppression via shRNA. They also replaced cMYC with non-transforming LMYC (small cell lung carcinoma associated MYC) to enhance safety of the hiPSCs. These episomal plasmids express 5 reprogramming factors: OCT4, LIN28, SOX2, KLF4, LMYC and shRNA for TP53^17,18. These vectors are maintained extra-chromosomally and lost from the reprogrammed cells upon continuous culture, thus making the lines transgene-free within 10-15 passages. Nucleofection is a specialized form of electroporation that delivers nucleic acids directly into the nucleus of host cells. It is an efficient method for delivery of the reprogramming plasmids into various cell types. Episomal plasmids are cost effective and compensate the high costs of nucleofection. This method is efficient and reproducible under optimized conditions yielding stable iPSCs from a variety of somatic cells. In this protocol, we describe the method for generation of iPSCs from fibroblasts isolated from fetal tissue by nucleofection of episomal reprogramming plasmids. Here are the detailed protocols for fibroblast isolation from fetal chorionic villi, plasmid purification, nucleofection, picking of colonies from the reprogramming plate and establishment of stable iPSCs.

It is essential to confirm the presence of pluripotency traits in the newly generated iPSCs. This includes demonstration of pluripotency related factors (e.g., alkaline phosphatase expression, NANOG, SSEA4, Tra 1-80, Tra 1-81, E-cadherin; usually shown with immunofluorescence or gene expression assays), identification of the three germ layers by in vitro differentiation assays to validate their differentiation potentials, karyotyping to determine chromosomal content, STR typing to establish identity with parent cells, verify loss of exogenous genes, and more stringent in vivo assays such as teratoma formation and tetraploid complementation. Here we describe characterization protocols of karyotyping, live cells alkaline phosphatase staining, detection of pluripotency related biomarkers by immunofluorescence, in vitro differentiation assays and method to demonstrate loss of exogenous genes¹⁹.

Protokół

FCV were obtained from Manipal Hospital, Bengaluru, under Ethics Committee of Manipal Hospitals approval.

NOTE: See Table 1 for composition of all buffers and solutions.

1. Isolation of fibroblasts from fetal chorionic villi (FCV)

1. Sample collection and tissue disintegration in collagenase
   1. Collect FCV under sterile conditions in phosphate buffered saline (PBS) and transport (at room temperature) to the cell culture facility.
   2. Transfer the villi to a 60 mm Petri dish and wash several times (minimum 4 times) in PBS containing 1x Antibiotic Antimycotic solution (PBS-AA).Remove PBS-AA completely by pipetting.
   3. Treat the chorionic villi with 1 mL collagenase blend (5 mg/mL) for 5 min at 37 °C.
   4. Neutralize with cell culture medium containing 10% fetal bovine serum (FBS), transfer digest to a 15 mL tube and centrifuge at 225 x g for 5 minutes to collect the disintegrated villi and released cells as a pellet.
2. Subculture and stock expansion
   1. Plate disintegrated villi along with released cells in a T25 culture flask containing 5 mL of complete media (e.g., AmnioMAX) and grow till a confluent fibroblast culture is obtained.
   2. Expand fibroblasts in culture to prepare stocks for use in subsequent transfection and characterization experiments as follows:
      1. Add 2 mL of 0.05% trypsin to T25 flask containing FCV fibroblasts and incubate at 37 °C for 3-5 min to dissociate the cells.
      2. After incubation, neutralize trypsin by adding FBS (at the same volume as trypsin).
         NOTE: Culture medium containing FBS can also be used to neutralize trypsin, when added at a 1:3 trypsin: media ratio.
      3. Collect the dissociated cells in a 15 mL tube and centrifuge at 225 x g for 5 min to obtain cell pellet.
      4. Decant supernatant and resuspend cell pellet in 1 mL of complete media.
      5. Transfer 500 µL each to 60 mm tissue culture-treated dishes and make up the volume to 5 mL. This splitting ratio of 1:2, was also used for subsequent passages.
3. Cryopreservation
   1. Perform enzymatic dissociation using 0.05% trypsin as described in steps 1.2.2.1 - 1.2.2.3 and obtain cell pellet.
   2. Discard the supernatant and resuspend the cell pellet in 1 mL of freezing mix, comprising 1:9 dimethyl sulfoxide (DMSO): FBS.
   3. Transfer contents to a sterile cryovial and place the vial in a freezing container.
   4. Freeze overnight at -80 °C and then transfer vials to liquid nitrogen (-196 °C) the next day.

2. Plasmids DNA Isolation and verification

1. Bacterial Cell Preparation
   1. Streak glycerol stocks of E. coli containing the three individual plasmids pCXLE-hOCT3/4-shp53-F, pCXLE-hSK and pCXLE-hUL (from Addgene) on separate Luria Bertani-ampicillin agar plates.
   2. Inoculate single colonies into starter cultures of 5 mL of Luria Bertani-ampicillin medium. Incubate for 8 hours at 37 °C with shaking (10 x g).
   3. Inoculate 200 µL of this starter culture into 100 mL of Luria Bertani-ampicillin medium. Incubate overnight at 37 °C with shaking.
   4. Harvest overnight bacterial culture by centrifuging at 6000 x g for 15 min at 4 °C.
2. Plasmid isolation with Midi Plasmid purification kit
   1. Resuspend bacterial pellet in 4 mL resuspension buffer.
   2. Add 4 mL of lysis buffer and mix thoroughly by vigorously inverting 4-6 times and incubate at room temperature for 5 min.
   3. Add 4 mL of pre-chilled neutralization buffer and invert tube 4-6 times to mix thoroughly. Incubate on ice for 15 min.
   4. Centrifuge at ≥20,000 x g for 30 min at 4 °C. Collect supernatant in a fresh tube and re-centrifuge at ≥20,000 x g for 15 min at 4 °C.
   5. Equilibrate the column by applying 4 mL of equilibration buffer.
   6. Apply the supernatant to the column.
   7. Wash the column twice with 10 mL of wash buffer.
   8. Elute DNA with 5 mL of warm (65 °C) elution buffer.
   9. Precipitate DNA by adding 3.5 mL of isopropanol to the eluted DNA. Mix well. Centrifuge at ≥15,000 x g for 30 min at 4 °C. Decant supernatant carefully.
   10. Wash the DNA pellet with 2 mL of 70% ethanol and centrifuge at ≥15,000 x g for 10 min. Decant supernatant carefully.
   11. Air-dry pellet for 5-10 min and dissolve DNA in a suitable volume of PCR-grade water to obtain a final concentration of 1 µg/mL.
       ​NOTE: Do not dissolve DNA in buffers as it is not suitable for electroporation. Old plasmid DNA preparation do not yield reprogrammed colonies.
3. Plasmid Verification by EcoRI restriction digestion
   1. Combine 15 µL of nuclease-free water, 2 µL of 10x buffer, 1 µg of plasmid DNA and 1 µL of EcoRI enzyme. Mix gently.
   2. Incubate the mixture at 37 °C for 15 min in a heat block.
   3. Mix the digested plasmid samples with 6x DNA gel loading dye and electrophorese on 1% agarose gel in 1x TAE buffer with 0.5 µg/mL of ethidium bromide. Include standard DNA ladder. Image the gel after the DNA has resolved appropriately. Expected EcoRI band sizes of pCXLE-hOCT3/ 4-shp53-F are 6,834 bp, 3,758 bp, and 1,108 bp; pCXLE-hUL are 10,200 bp and 1,900 bp; pCXLE-hSK are 10,200 bp and 2,500 bp.

3. Nucleofection

1. Cell pelleting
   1. Culture the isolated fetal chorionic villi fibroblasts in T25 flask in 5 mL of complete media till 80-90% confluency.
   2. Wash cells twice with PBS and trypsinize as described in steps 1.2.2.1 - 1.2.2.3.
   3. Remove the supernatant, resuspend pellet in 5 mL of reduced serum media (e.g., Opti-MEM). Count cells with hemocytometer and take 10⁶ cells for nucleofection. Centrifuge at 225 x g for 5 min. Remove supernatant completely.
2. Reagent preparation and nucleofection
   1. Prepare nucleofector reagent by mixing 0.5 mL of supplement and 2.25 mL of nucleofector solution (both provided in the kit).
   2. Add 100 µL of nucleofector solution in a 1.5 mL tube. Add 1µg each of pCXLE-hOCT3/4-shp53-F, pCXLE-hSK and pCXLE-hUL to the tube. Gently resuspend 10⁶ cells (from step 3.1.2) in this mix.
   3. Transfer the cell-DNA suspension into cuvette, ensuring that the sample covers the bottom of the cuvette (provided in kit) without any air bubbles. Cap the cuvette and insert into the holder. Select the nucleofector Program U-23 (for high efficiency) and apply.
   4. Remove cuvette out of the holder and add 1 mL of complete media. Transfer the contents gently into a 60 mm tissue culture treated Petri dish filled with 4 mL of complete media (to a total of 5 mL of media). Incubate the cells in a humidified CO₂ incubator at 37 °C.
   5. After 24 h, check if the cells have attached. Replace the medium completely.
      NOTE: The rate of cell death is high in nucleofection leaving few viable cells which attach.
   6. Maintain the cells in complete media for 10 days and shift to pluripotency media for the next 20 days.
      ​NOTE: Visualize cells regularly to follow morphological changes occurring in the reprogramming cells (like epithelial morphology and compact colony formation) to confirm if the experiment is working. Around 25 iPSC colonies can be seen after 20 days of culture in pluripotency media.

4. Picking and propagation of iPSC colonies

1. Picking colony from reprogramming plate
   1. Manually dissect the embryonic stem cell-like colonies formed in the reprograming dish using pulled glass pipettes or 1 mL syringe needles and transfer to previously prepared plate with inactivated mouse embryonic fibroblast feeders with pluripotency medium or establish feeder free cultures on Matrigel coated plates with mTESR medium.
      ​NOTE: Mouse embryonic fibroblasts (MEFs) were derived using enzymatic isolation from mouse embryos (dissected from 13-14 days pregnant female mice) and were mitotically inactivated by mitomycin C treatment. Establish single clone populations by growing single colonies from reprogramming plate in separate dishes or mixed clone populations by transferring many colonies from reprogramming plate to a single dish.
2. Mechanical transfer of emerging colonies to fresh feeders and passaging to establish stable iPSCs
   1. Propagate iPSCs in pluripotency medium by feeding every second day and split 1:3 every 5-7 days. Prepare stocks by cryopreserving in a freezing mix of KnockOut Serum Replacement and DMSO in the ratio 9:1.
      NOTE: KnockOut Serum Replacement is used in the freezing mix for cryopreservation of iPSCs instead of FBS as components in the FBS could induce differentiation of the pluripotent cells during long term preservation.

5. Characterisation of iPSCs

NOTE: Characterization studies including PCR and immunostaining for pluripotency biomarker were done after the fifth passage number. Karyotyping was performed at a later passage number.

1. Karyotyping
   1. Treat a confluent 60 mm Petri dish of iPSCs with colcemid for 45 min in humidified CO₂ incubator at 37 °C.
   2. Harvest by 0.05% trypsin treatment and centrifuge. Remove the supernatant and pipette the leftover traces of medium to loosen the cell pellet.
   3. Add 5 mL of hypotonic solution. Mix by inverting tube and incubate for 20 minutes at 37 °C. Centrifuge at 225 x g for 5 min.
      NOTE: The obtained pellet should appear fluffy.
   4. Add 2.5 mL of Carnoy's fixative solution slowly, while tapping to loosen the pellet.
   5. Prepare spreads for karyotyping by dropping the cell suspension on clean glass slides.
   6. Treat the slides with 0.15% trypsin for 1 minute, and wash once with PBS. Then stain with Giemsa solution for 4 min and end with a distilled water wash. Acquire and process with appropriate software.
2. Demonstration of transgene free status
   1. Genomic DNA Isolation
      1. Pipette 20 µL of protease into the bottom of a 1.5 mL microcentrifuge tube.
      2. Add 200 µL of TSiPSCs resuspended in PBS to the microcentrifuge tube.
      3. Add 200 µL of Buffer AL to the sample and mix for 15 s by pulse-vortexing.
      4. Incubate for 10 min at 56 °C.
      5. Briefly centrifuge the microcentrifuge tube to remove drops from the inside of the lid.
      6. Add 200 µL of ethanol (96-100%) to the sample, and mix again for 15 s by pulse-vortexing. After mixing, briefly centrifuge the tube to remove drops from the inside of the lid.
      7. Carefully apply the mixture from the previous step to the mini spin column (in a 2 mL collection tube) without wetting the rim. Close the cap, and centrifuge at 6000 x g for 1 min. Discard the tube containing the filtrate and place the mini spin column in a clean 2 mL collection tube.
      8. Carefully open the mini spin column and without wetting the rim, add 500 µL of Buffer AW1. Close the cap and centrifuge at 6000 x g for 1 min. Place the mini spin column in a clean 2 mL collection tube and discard the collection tube containing the filtrate.
      9. Carefully open the mini spin column and add 500 µL of Buffer AW2 without wetting the rim. Close the cap and centrifuge at full speed (20,000 x g) for 3 min.
      10. Place the mini spin column in a new 2 mL collection tube and discard the old collection tube with the filtrate. Centrifuge at full speed for 1 min to eliminate the chance of possible Buffer AW2 carryover.
      11. Place the mini spin column in a clean 1.5 mL microcentrifuge tube, and discard the collection tube containing the filtrate. Carefully open the mini spin column and add 200 µL Buffer AE or distilled water. Incubate at room temperature (15-25 °C) for 5 min, and then centrifuge at 6000 x g for 1 min.
   2. Transgene-Free Status PCR (Using KAPA HiFi PCR Kit KR0368)
      1. Ensure that all reagents are properly thawed and mixed.
      2. Prepare a PCR master mix containing the appropriate volume of all reaction components based on Table 2 (set up reactions on ice).
      3. Transfer the appropriate volumes of PCR master mix, template and primer to individual PCR tubes.
      4. Cap individual reactions, mix and centrifuge briefly.
      5. Perform PCR following Table 3.
3. Pluripotency biomarker identification
   1. Alkaline phosphatase (AP) staining
      1. Prepare a 1x AP live stain working solution by diluting 3 µL of 500x stock solution in 1.5 mL DMEM/F-12 for every 10 cm² of culture area.
      2. Remove the medium from the iPSC culture dish. Wash the culture with DMEM/F-12 once. Add the 1x AP live stain solution onto the iPSCs. Incubate at 37 °C for 45 min.
      3. Remove the AP stain and wash twice with DMEM/F-12. Add fresh DMEM/F-12 and image under fluorescent microscope using a standard FITC filter within 30-90 min of staining.
   2. Immunostaining for pluripotency biomarkers
      1. Fix confluent iPSC cultures with 4% paraformaldehyde overnight at 4 °C. Wash thrice with PBS Tween 20 (PBST), each wash for 5 min.
      2. Permeabilize the cells with 0.3% Triton X-100 in PBST for 15 minutes at room temperature. Wash thrice with PBST.
         ​NOTE: Permeabilization should be done only for intracellular antigens.
      3. Block cells with 3% bovine serum albumin (BSA) in PBST for 30 min at room temperature. Stain the cells with primary antibodies (diluted 1:1000 in 1% BSA) overnight. After primary antibody incubation, wash thrice with PBST.
      4. Incubate cells with the secondary antibody (diluted 1:1000 in 1% BSA) for 5 h at room temperature.Wash thrice with PBST.
      5. Label the nuclei with 0.5 µg/mL 4',6-diamidino-2-phenylindole (DAPI) for 1 minute. Wash the cells once with PBST.
      6. Capture images under fluorescent microscope.

6. ​In vitro differentiation assays

1. Embryoid Body (EB) Differentiation
   1. Cut the iPSC colonies into small pieces, collect and plate in low attachment Petri dishes in embryoid body medium. Grow the cells for 15 days by replacing medium every 3 days.
      NOTE: The day 15 EBs can be used directly for detection of the three germ layer biomarkers. Alternatively, specific cell lineages can be induced with growth factors, followed by biomarker detection.
2. Endoderm (Hepatocyte) differentiation
   1. Grow the iPSCs in monolayer cultures in pluripotency medium.
   2. Once confluent, shift to RPMI 1640 media with 1x Insulin Transferrin Selenite and 100 ng/mL activin A for 2 days, followed by growth in RPMI 1640 media with 30 ng/mL bFGF and 20 ng/mL BMP4 for 9 days. Replace medium every 2 days.
   3. From day 10 onwards, supplement media with 0.1 µM dexamethasone. Terminate the experiment on day 20.
3. Mesoderm (Cardiomyocyte) differentiation
   1. Plate day 8 EBs on 0.5% Matrigel-coated plates in embryoid body medium. Allow the EBs to attach and collapse.
   2. Supplement media with 20 ng/mL BMP4 and grow for 20 days. Replace medium every 2-3 days. Terminate the experiment on day 20.
4. Ectoderm (Neuronal) differentiation
   1. Plate day 4 EBs on 2 µg/cm² collagen type IV-coated plates in embryoid body medium.Allow the EBs to attach and collapse.
   2. Next day, shift medium to DMEM F-12 with 2mg/mL glucose, 1x Insulin Transferrin Selenite, and 2.5µg/mL fibronectin. Terminate the experiment on day 15.
5. Formation of cerebral organoids
   1. Grow TSiPSCs in a 35 mm tissue culture dish on MEFs till 70-80% confluent. Cut the colonies and collect in a 15 mL tube. Centrifuge the cells at 225 x g for 5 min. Discard the supernatant.
   2. Wash the pieces of colonies by resuspending in 2 mL of PBS and centrifuge to remove the supernatant.
   3. Add 1 mL of 0.05% trypsin and tap the tube to dislodge the cells. Incubate the tube at 37 °C for 3-4 min to dissociate the colony pieces into a single cell suspension.
   4. Neutralize the trypsin by dilution with 4 mL of pluripotency media containing 10 µg/mL rho-associated protein kinase (ROCK) inhibitor Y-27632 dihydrochloride (ROCKi) to prevent dissociation induced cell death.
   5. Centrifuge to obtain a pellet. Discard the supernatant and resuspend the cells in 2mL embryoid body medium containing 10 µg/mL ROCKi.
   6. Remove 10 µL of cell suspension for cell counting. Add 10 µL of Trypan blue to detect dead cells. Count the cells using a hemocytometer.
   7. Add appropriate volume of embryoid body medium with ROCKi to the cell suspension to obtain 9,000 live cells per 150 µL.
   8. Plate 150 µL in each well of a low-attachment 96-well plate and incubate in a humidified CO2 incubator at 37 °C. Check the plates for aggregation after 24 hours. On day 2 gently remove the medium and replace with fresh embryoid medium without ROCKi.
   9. On day 6, transfer EBs to wells of a low attachment 24 well plate containing 500 µL of neural induction medium composed of DMEM-F12 with 1% N2 supplement, 2 mM GlutaMAX supplement and 1 mM non-essential amino acids and 1 µg/mL heparin. Change the medium every 2 days.
   10. After 5 days in neural induction medium embed the neuroepithelial aggregates in Matrigel by layering a 2 cm x 2 cm square of parafilm over an empty tip tray of 200 µL tips. Press parafilm with gloved fingers over each hole in the tip tray to make small dents. Clean parafilm with 70% ethanol to sterilize.
   11. Transfer the parafilm square into a 60 mm dish. Use cut 200 µL tips to transfer the neuroepithelial aggregates onto the dents in parafilm. Remove excess medium by pipetting.
   12. Add 30 µL of thawed Matrigel on the neuroepithlial aggregates and position the aggregate to the center of the Matrigel using a pipette tip. Place the 60 mm dish for 20-30 min in a 37 °C incubator for the Matrigel to polymerize.
   13. Add 5 mL of cerebral organoid differentiation medium composed of 1:1 DMEM-F12: Neurobasal medium, 0.5% N2 supplement, 2.5 µg/mL of insulin, 2 mM GlutaMAX supplement, 0.5 mM NEAA, 1% B27 supplement and 2.5 mL of penicillin-streptomycin.
   14. Using a sterile forceps turn the parafilm sheet over and agitate the dish until the Matrigel embedded aggregates fall off the sheet into the medium. Grow the embedded aggregates in a humidified CO₂ incubator at 37 °C for 4 days giving media changes on alternate days.
   15. After 4 days of static culture place the 60 mm dishes onto an orbital shaker installed inside the incubator shaking at 50 rpm. Culture the organoids for 3 months giving complete media changes with cerebral organoid differentiation medium every 3 days.

Wyniki

Generation of integration-free iPSCs from a spontaneously aborted fetus with 45XO karyotype
We isolated fibroblasts from FCV with a Turner syndrome (TS) specific 45XO karyotype and nucleofected them with episomal reprogramming plasmids to generate TSiPSCs which can be used for downstream modelling of the syndrome, specifically the associated neurological deficits (Figure 1a&b). We used nonintegrating episomal vectors and nucleofection for the trans...

Dyskusje

Generation of stable cellular models of cytogenetically abnormal fetal tissue is necessary for perpetuating defective phenotype. The iPSC route is the most effective method of cell preparation for perpetual conservation of defective properties²⁰.

Pluripotent stem cells (PSC) display properties of self-renewal and differentiation into specialized cells reminiscent of early cleavage embryos²¹. Hence, PSCs can serve as excellent models to study earl...

Materiały

Name	Company	Catalog Number	Comments
0.15% trypsin	Thermo Fisher Scientific	27250018	G Banding
2-mercaptoethanol	Thermo Fisher Scientific	21985023	Pluripotency and Embryoid body medium
4', 6 diamidino-2-phenylindole	Sigma Aldrich	D8417	Immunocytochemistry
Activin A	Sigma Aldrich	SRP3003	Differentiation assays
Alkaline Phosphatase Live Stain	Thermo Fisher Scientific	A14353	AP staining
AMAXA Nucleofector II	Lonza	-	Nucleofection
AmnioMAX II complete media	Thermo Fisher Scientific, Gibco	11269016	Medium specific for foetal chorionic villi cell cultures
Ampicillin	HiMedia	TC021	Plasmid purification
Anti Mouse IgG (H+L) Alexa Fluor 488	Invitrogen	A11059	Immunocytochemistry
Anti Rabbit IgG (H+L) Alexa Fluor 488	Invitrogen	A11034	Immunocytochemistry
Anti Rabbit IgG (H+L) Alexa Fluor 546	Invitrogen	A11035	Immunocytochemistry
Antibiotic-Antimycotic	Thermo Fisher Scientific, Gibco	15240096	Contamination control
Anti-E-Cadherin	BD Biosciences	610181	Immunocytochemistry
Anti-Nanog	BD Biosciences	560109	Immunocytochemistry
Anti-OCT3/4	BD Biosciences	611202	Immunocytochemistry
Anti-SOX17	BD Biosciences	561590	Immunocytochemistry
Anti-SOX2	BD Biosciences	561469	Immunocytochemistry
Anti-SSEA4	BD Biosciences	560073	Immunocytochemistry
Anti-TRA 1-81	Millipore	MAB4381	Immunocytochemistry
basic Fibroblast Growth Factor[FGF2]	Sigma Aldrich	F0291	Pluripotency medium
Bone Morphogenetic Factor 4	Sigma Aldrich	SRP3016	Differentiation assays
Bovine Serum Albumin	Sigma Aldrich	A3059	Blocking
Collagen Human Type IV	BD Biosciences	354245	Differentiation assays
Collagenase blend	Sigma Aldrich	C8051	Digestion of foetal chorionic villi
Dexamethasone	Sigma Aldrich	D4902	Differentiation assays
DMEM F12	Thermo Fisher Scientific	11320033	Differentiation assays
FastDigest EcoR1	Thermo Scientific	FD0274	Restriction digestion
Fibronectin	Sigma Aldrich	F2518	Differentiation assays
Giemsa Stain	HiMedia	S011	G Banding
Glacial Acetic Acid	HiMedia	AS001	Fixative for karyotyping
Glucose	Sigma Aldrich	G7528	Differentiation assays
GlutaMAX	Thermo Fisher Scientific	35050061	Pluripotency and Embryoid body medium
Heparin sodium	Sigma Aldrich	H3149	Differentiation assays
Insulin solution human	Sigma Aldrich	I9278	Differentiation assays
Insulin Transferrin Selenite	Sigma Aldrich	I1884	Differentiation assays
KAPA HiFi PCR kit	Kapa Biosystems	KR0368	OriP, EBNA1 PCR
KaryoMAX Colcemid	Thermo Fisher Scientific	15210040	Mitotic arrest for karyotyping
KnockOut DMEM	Thermo Fisher Scientific	10829018	Pluripotency and Embryoid body medium
KnockOut Serum Replacement	Thermo Fisher Scientific	10828028	Pluripotency and Embryoid body medium
Luria Bertani agar	HiMedia	M1151F	Plasmid purification
Matrigel	BD Biosciences	356234	Differentiation assays
MEM Non-essential amino acids	Thermo Fisher Scientific	11140035	Pluripotency and Embryoid body medium
Methanol	HiMedia	MB113	Fixative for karyotyping
Myosin ventricular heavy chain α/β	Millipore	MAB1552	Immunocytochemistry
NHDF Nucleofector Kit	Lonza	VAPD-1001	Nucleofection
Paraformaldehyde (PFA)	Sigma Aldrich	P6148	Fixing cells
pCXLE-hOCT3/ 4-shp53-F	Addgene	27077	Episomal reprogramming Plasmid
pCXLE-hSK	Addgene	27078	Episomal reprogramming Plasmid
pCXLE-hUL	Addgene	27080	Episomal reprogramming Plasmid
Penicillin Streptomycin	Thermo Fisher Scientific,	15070063	Pluripotency and Embryoid body medium
Phalloidin- Tetramethylrhodamine B isothiocyanate	Sigma Aldrich	P1951	Immunocytochemistry
Phosphate buffered saline	Sigma Aldrich	P4417	1 X PBS 1 tablet of PBS dissolved in 200mL of deionized water and sterilized by autoclaving Storage: Room temperature. PBST- 0.05% Tween 20 in 1X PBS. Storage: Room temperature.
Plasmid purification Kit- Midi prep	QIAGEN	12143	Plasmid purification
Potassium Chloride Solution	HiMedia	MB043	Hypotonic solution for karyotyping
QIAamp DNA Blood Kit	Qiagen	51104	Genomic DNA isolation
RPMI 1640	Thermo Fisher Scientific	11875093	Hepatocyte differentiation medium
Sodium Citrate	HiMedia	RM255	Hypotonic solution for karyotyping
Triton X-100	HiMedia	MB031	Permeabilisation
Trypsin-EDTA (0.05%)	Thermo Fisher Scientific, Gibco	25300054	Subculture of  foetal chorionic villi fibroblasts
Tween 20	HiMedia	MB067	Preparation of PBST
β III tubulin	Sigma Aldrich	T8578	Immunocytochemistry
Y-27632 dihydrochloride	Sigma Aldrich	Y0503	Differentiation assays