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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol aims to stably plate dorsal-ventral fused assembloids on multi-electrode arrays for modeling epilepsy in vitro.

Abstract

Human brain organoids are three-dimensional (3D) structures derived from human pluripotent stem cells (hPSCs) that recapitulate aspects of fetal brain development. The fusion of dorsal with ventral regionally specified brain organoids in vitro generates assembloids, which have functionally integrated microcircuits with excitatory and inhibitory neurons. Due to their structural complexity and diverse population of neurons, assembloids have become a useful in vitro tool for studying aberrant network activity. Multi-electrode array (MEA) recordings serve as a method for capturing electrical field potentials, spikes, and longitudinal network dynamics from a population of neurons without compromising cell membrane integrity. However, adhering assembloids onto the electrodes for long-term recordings can be challenging due to their large size and limited contact surface area with the electrodes. Here, we demonstrate a method to plate assembloids onto MEA plates for recording electrophysiological activity over a 2-month span. Although the current protocol utilizes human cortical organoids, it can be broadly adapted to organoids differentiated to model other brain regions. This protocol establishes a robust, longitudinal, electrophysiological assay for studying the development of a neuronal network, and this platform has the potential to be used in drug screening for therapeutic development in epilepsy.

Introduction

Human pluripotent stem cell (hPSC)-derived brain organoids are spatially self-organized 3D structures mirroring the tissue architecture and developmental trajectories in vivo. They are composed of multiple cell types, including progenitors (neuroepithelial cells, radial glia, neuronal progenitors, glial progenitors), neurons (cortical-like excitatory neurons and inhibitory interneurons), and glial cells (astrocytes and oligodendrocytes)1,2. Assembloids represent the next generation of brain organoids, capable of integrating multiple brain regions and/or cell lineages within a 3D culture. They provide ....

Protocol

All experimental procedures demonstrated below were conducted in accordance with the ethical guidelines of the University of Michigan Medical School Institutional Review Board and the Human Pluripotent Stem Cell Research Oversight Committee. The iPSC lines used in this protocol and the representative experiments were derived from human foreskin fibroblasts obtained from a commercial source. The details of the cell lines, reagents, and equipment used in this study are listed in the Table of Materials.

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Representative Results

Human dorsal-ventral assembloids were plated on a 6-well MEA plate (n = 6 per differentiation, 3 differentiations), with each well containing 64 electrodes (Figure 2A). Nine out of ten assembloids planned for longitudinal recording were firmly attached to the electrodes for over 50 days in vitro (Figure 2D). 6 out of 8 assembloids designated for pharmacological assays were successfully settled through the wash-out phase .......

Discussion

MEA-based methods for electrophysiological recordings of network activity in iPSC-derived assembloids have been used for in vitro modeling of epilepsy22,23. This proposed platform integrating excitatory and inhibitory synaptic connections has the potential to address mechanisms of neuronal hyperexcitability and the role of cortical interneurons in the process of epileptogenesis. Additionally, this platform allows for the stabilization of assembloids and .......

Acknowledgements

This manuscript was supported by R01NS127829 NIH/NINDS (LTD). Figure 1 has been generated using biorender.com.

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Materials

NameCompanyCatalog NumberComments
10 cm Corning Non TC-treated culture dishesCorning08-772-32For suspension culture on the shaker
100 mL Beaker Fisher ScientificFB100100
100% EthanolFisher ScientificBP28184-4L
2-Mercaptoethanol (β-ME)Thermo Fisher21985023Working concentration 100 μM
48-well cell culture plateFisher Scientific50-202-140
6-well cell culture plateFisher Scientific07-200-83
Aggrewell 800Fisher Scientific501974754
Allegra X-14R Refrigerated CentrifugeBeckman Coulter BE-AX14R
AllopregnanoloneCayman16930Suspended 5mg into DMSO to get 1 mM stock solution. Aliquot and freeze at −80 °C. Dilute at 1:10,000 for use. Working concentration 100 nM.
Automated cell counterThermo FisherAMQAX2000
Axion CytoView MEA 6-well plates Axion BiosystemsM384-tMEA-6B
Axion Maestro MEA platformAxion BiosystemsMaestroWith temp environmental control
B-27 supplement (regular, with Vitamin A)Thermo Fisher21985023
B-27 supplement (without Vitamin A)Thermo Fisher12587010
Basement membrane matrix- GeltrexThermo FisherA1569601
Bead bathFisher Scientific10-876-001Isotemp
Benchtop inverted microscopeOlympusCKX53Kept in laminar flow clean bench
BicucullineSigma-Aldrich14340Working concentration 10 μM
BleachCLOROX67619-26
Borate buffer 20xThermo Fisher28341Working concentration at 1x
BrainPhys mediaStemCell Technologies5790
Cell dissociation reagent (StemPro Accutase)Thermo FisherA1110501
Celltron orbital shakerHT-Infors I69222 
Detergent/enzyme (Terg-A-Zyme)Sigma-AldrichZ273287Working concentration 1% m/v
DMEM/F12 + HEPES/L-GlutamineThermo Fisher113300
DMSOSigma-Aldrich67685
DorsomorphinSigma-AldrichP5499Dissolve 5mg into DMSO to get 10 mM stock solution. Aliquot and freeze at −20 °C. Dilute at 1:2000 for use. (working concentration 5 μM)
D-PBS w/o calcium or magnesiumThermo Fisher14190144
Glial cell line-derived neurotrophic (GDNF)Peprotech450-10Dissolve 100 μg in 1mL of PBS to 100 μg/mL. Aliquot and freeze at −20 °C. Dilute at 1:5000 for use. (working concentration 20 ng/mL).
GlutaMAX supplementThermo Fisher35050061
HemacytometerElection Microscopy Sciences63510-20
HEPESThermo Fisher15630080
Heraguard ECO Clean BenchThermo Fisher51029692
Humidity controlled cell culture incubatorThermo Fisher370set to 37 °C, 5% CO2
IWP-2SelleckchemS7085Aliquot and freeze at −80 °C. It will precipitate if thawed at room temp. Frozen aliquots should be placed directly into 37 °C before use.
Knockout serum replacement (KOSR)Thermo Fisher10828010
mTeSRplus (medium + supplements)StemCell Technologies100-0276cGMP, stabilized feeder-free medium for human iPSC cells
N2 supplementThermo Fisher17502048
Neurobasal AThermo Fisher21103049
Non-essential amino acids (NEAA)Thermo Fisher11140050
NT3Peprotech450-03Dissolve 100 μg in 1mL of PBS to 100 μg/mL. Aliquot and freeze at −20 °C. Dilute at 1:5000 for use. (working concentration 20 ng/mL).
NuFF Human neonatal foreskin fibroblastsMTI-GlobalStemGSC-3002
ParafilmPARAFILMP7793
Penicilin/StreptomycinThermo Fisher15140122
Pipette (P10, P200, P1000)EppendorfEP4926000034Autoclaved cut P1000 tips for organoid collection
Poly (Ethyleneimine) (PEI)Sigma-AldrichP3143Dilute stock in sterile borate buffer. Working concentration 0.07%. See details in manuscript.
Recombinant human epidermal growth factor (EGF)R&D Systems236-EG-200Suspended in PBS. Aliquot and freeze at -20 °C.
Recombinant Human fibroblast growth factor (FGF)-basic Peprotech100-18BSuspended in PBS. Aliquot and freeze at -20 °C.
Recombinant human-brain-derived neurotrophic factor (BDNF)Peprotech450-02Centrifuge briefly before reconstitution. Dissolve 100 μg in 1 mL of PBS to 100 μg/mL. Aliquot and freeze at −20 °C. Dilute at 1:5000 for use. (working concentration 20 ng/mL).
Retinoic acid (RA)Sigma-AldrichR2625Dissolve 100 mg into 3.3 mL of DMSO to get 100 mM stock solution. Aliquot the stock 100 μL/tube and freeze at −80 °C. Take 200 μL of 100 mM stock and dilute 10x (add 1.8 mL of DMSO) to make 10 mM stock. Aliquot 50 μL/tube and store at −80 °C. Dilute at 1:100,000 for use. (working concentration 100 nM).
ROCK inhibitor Y-27632Tocris12541:200 from 10 mM stock
SAG (smoothened agonist)SelleckchemS7779Aliquot and freeze at −80 °C. Stock concentration 1mM. Use at 1:10,000 dilution (working concentration 100 nM).
SB-431542Tocris1614Dissolve 5mg into 1.3 mL of DMSO to get 10 mM stock solution. Aliquot and freeze at −80 °C. Dilute at 1:1000 for use. (working concentration 10 μM)
Serological pipette fillerFisher Scientific14-387-166
Steriflip vacuum tube top filterSigma-AldrichSE1M179M6
Sterile cell culture hoodsBaker CompanySG-600
Trypan blue solution (0.4%)Thermo Fisher15250061
Trypsin-EDTA (0.25%)Thermo Fisher25200056
Zoom stereomicroscopeOlympusSZ61/SZ51Kept in laminar flow clean bench

References

  1. Lancaster, M. A., Knoblich, J. A. Organogenesis in a dish: Modeling development and disease using organoid technologies. Science. 345 (6194), 1247125 (2014).
  2. Tanaka, Y., et al.

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