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In This Article

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

Summary

Recent works uncover the neuronal impact on high-grade pediatric glioma (pHGG) cells and their reciprocal interactions. The present work shows the development of an in vitro model co-culturing pHGG cells and glutamatergic neurons and recorded their electrophysiological interactions to mimic those interactivities.

Abstract

Pediatric high-grade gliomas (pHGG) represent childhood and adolescent brain cancers that carry a rapid dismal prognosis. Since there is a need to overcome the resistance to current treatments and find a new way of cure, modeling the disease as close as possible in an in vitro setting to test new drugs and therapeutic procedures is highly demanding. Studying their fundamental pathobiological processes, including glutamatergic neuron hyperexcitability, will be a real advance in understanding interactions between the environmental brain and pHGG cells. Therefore, to recreate neurons/pHGG cell interactions, this work shows the development of a functional in vitro model co-culturing human-induced Pluripotent Stem (hiPS)-derived cortical glutamatergic neurons pHGG cells into compartmentalized microfluidic devices and a process to record their electrophysiological modifications. The first step was to differentiate and characterize human glutamatergic neurons. Secondly, the cells were cultured in microfluidic devices with pHGG derived cell lines. Brain microenvironment and neuronal activity were then included in this model to analyze the electrical impact of pHGG cells on these micro-environmental neurons. Electrophysiological recordings are coupled using multielectrode arrays (MEA) to these microfluidic devices to mimic physiological conditions and to record the electrical activity of the entire neural network. A significant increase in neuron excitability was underlined in the presence of tumor cells.

Introduction

Pediatric high-grade gliomas (pHGG) exhibit an extended genotypic and phenotypic diversity depending on patient age, tumor anatomical location and extension, and molecular drivers1. They are aggressive brain tumors that are poorly controlled with the currently available treatment options and are the leading cause of death related to brain cancers in children and adolescents2. So, more than 80% of patients are relapsing within 2 years after their diagnosis, and their median survival is 9-15 months, depending on brain locations and driver mutations. The absence of curative treatment is the primary urge for laboratory resea....

Protocol

For this protocol, the accreditation number related to the use of human materials is DC-2020-4203.

1. Microfluidic device fabrication, preparation and treatment

  1. Fabricate SU-8 molds using conventional photolithography techniques18.
    NOTE: For this purpose, two photolithography masks have been designed to construct two layers of photoresist structures on silicon wafer substrate and a thin SU-8 2005 photoresist layer (3.2 µm high and 6 ± 1 µm wide) that defines asymmetric microgrooves under the patterning of main channels made in SU-8 2100 (200 µm high, 1 mm wide, and 13 mm long) (....

Results

Before studying electrical interactions between glutamatergic neurons and glioma cells, hiPS-derived cortical glutamatergic neurons were characterized to validate the feasibility of culturing them in microfluidic devices (Figure 1A). Their characterization was assessed using Nestin, Sox2, mGlurR2 (metabotropic Glutamate Receptors 2), and vGLUT1 immunostaining, represented in Figure 1A(2-7). As Nestin is an intermediate f.......

Discussion

This work describes an accurate functional in vitro model to evaluate the interaction between human hiPS-derived cortical glutamatergic neurons and brain tumoral cells in microfluidic devices. One of the crucial steps in the present protocol was the hiPS differentiation in glutamatergic neurons, which was confirmed by the decrease of Nestin and Sox2 immunofluorescent staining and simultaneous appearance of mGluR2 and vGLUT1 staining. Nevertheless, few neural progenitors remained as only half of the glutamatergic.......

Disclosures

AB, MG, JR, LM, ML, JV, DD are employed by NETRI, FL is Chief Technology Officer at NETRI, and TH is Chief Scientific Officer at NETRI. The other authors have nothing to disclose.

Acknowledgements

This work was supported by grants from Satt Conectus program, Fondation de l'Université de Strasbourg, «J'ai demandé la lune», «Une roulade pour Charline», «LifePink», «Franck, Rayon de Soleil» and «Semeurs d'Etoile» associations. We thank the children and families affected by HGGs for their contributions to this research and their support.

....

Materials

NameCompanyCatalog NumberComments
256MEA100/30iR-ITO-w/oMCS256MEA100/30iR-ITO-w/o
40 µm probe for Scepter counter Dutscher53750
60 µm probe for Scepter counter Dutscher51999
AccutaseSigmaA6964
Ala -Gln (GlutaMAX)SigmaG8541
Axel Observer 7 MicroscopeZeiss431007-9904-000
Cell culture flask with cap with filter membrane 70 mL Falcon®Dutscher353109
Class II Biological Safety CabinetThermo ScientificHERASafe type KS12
Colibri 7 LEDZeiss4230529710-000
Cortical Glutamatergic Neurons
BrainXellBX-0300
DMEM/F-12 (1:1) GlutaMAXGibco31331-028
DMEM/F12 MediumSigmaD8437
DPBS 1XDutscherL0615-500
EasYFlaskTM cell culture flasks 75cm3Nunc156499
Foetal Bovine Serum (FBS)Dutscher500105
GDNFPeprotech450-10
GeltrexLife TechnologiesA1413201
Human BDNFPeprotech450-02
IncubatorMemmertIC0150med
MCS InterFace BoarderMCS181205-MEA2100-11240
MEA2100MCS181205-MEA2100-11240
Micropipette P10SartoriusLH-729020
Micropipette P100SartoriusLH-729050
Micropipette P1000SartoriusLH-729070
Micropipette P200SartoriusLH-729060
Microtube Eppendorf 1,5 ml Safe-LockDutscher33290
MultiChannel ExperimenterMCS-
N2 Supplement-AStemCell7152
Neurobasal MediumLife Technologies21103049
Neurocult SM1 neuronal supplementStemCell5711
Non filter tip 0.1 - 10 µl ClearLine® sterile in removable-lid rack Dutscher030570ACL
Non filter tip 1 - 200 µl ClearLine® sterile in removable-lid rack Dutscher032260CL
Non filter tip 50 - 1250 µl ClearLine® sterile in removable-lid rackDutscher134760CL
Non-essential amino acids (NEAA) without L-glutamineDutscherX0557-100
Pipeteur Pipet-Aid XP GravityDrummond4000202/4038202
Pipette for cell culture 10 mL Falcon® Dutscher357551
Pipette for cell culture 5 mL Falcon® Dutscher357543
Plaque chauffante (CultureTemp)Belart370151000
Poly-D-LysineSigmaP6407
Primovert microscopeZeiss415510-1100-000
Scepter (Handheld Automated Cell Counter)MilliporePHCC00000
TGF-β1Peprotech100-21C
Tube with conical bottom 15 mL (bulk) Falcon® Dutscher352096
Tube with conical bottom 50 mL (bulk) Falcon® Dutscher352070

References

  1. Mackay, A., et al. Integrated molecular meta-analysis of 1,000 pediatric high-grade and diffuse intrinsic pontine glioma. Cancer Cell. 32 (4), 520-537 (2017).
  2. Ostrom, Q. T., et al.

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