Ultrasound-Induced Neuromodulation Using a Microelectrode Array System

Samenvatting

Source: Liang, R. et al., Focused Ultrasound Neuromodulation of Human In Vitro Neural Cultures in Multi-Well Microelectrode Arrays. J. Vis. Exp. (2024)

This video demonstrates the method for inducing the modulation of neural activity in cultured human iPSC-derived neurons in a multi-well microelectrode array, or MEA system using a focused ultrasound transducer.

Protocol

1. Preparation of materials

1. Aspirate the culture medium and use it to fill a single well in a 24-well neuron culture plate with an embedded microelectrode array (MEA) (Figure 1A).
2. Sterilize the parafilm interface, the rubber band, and the focused ultrasound (FUS) cone with its rubber membrane using 70% ethanol for 10 min, and place them in the fume hood for later assembly.
3. Degas 300 mL of deionized water and 50 mL of coupling gel. Centrifuge the water and gel at 160 x g for 5 min to avoid inducing cavitation within the coupling medium.
   NOTE: The original source of the human induced pluripotent stem cells (HiPSCs) is from GM01582 and CIPS cell lines. On average, a density of 5 x 10⁴ motor neurons and 2.5 x 10⁴ astrocytes per well can be achieved.

2. Connection and setup of the peripherals

1. Secure the FUS cone to the transducer using screws, and seal the cone with a flexible rubber membrane in a ventilated sterile hood. Fill the cone with the degassed and deionized (DG-DI) water from step 1.3, and ensure the absence of bubbles in the cone to avoid cavitation.
2. Use a customized threaded rod to secure the 3D-printed holder to a frame (Figure 1B). Position the frame such that the head of the FUS transducer is over the well that will be stimulated.
3. Use a rubber band to secure parafilm over the well on the 24-well MEA plate containing the medium and the HiPSCs.
4. Prepare the FUS system by connecting the ultrasound transducer's back-end driver electronics, in this case, the transducer power output (TPO), to a 100-240 V power outlet and connecting the matching network to the TPO and the FUS transducer. The matching network ensures efficient electrical coupling between the transducer and the TPO.
5. Connect the MEA system to a power outlet (100-240 V) (Figure 2B, Connection 5). Connect the MEA system synchronization port to the TPO (Figure 2B, Connection 3). This connection will synchronize the data acquisition by the MEA system with the FUS stimulation.
6. Place the 24-well MEA plate in the MEA system, and remove the lid to enable direct contact between the transducer and the well. Place the transducer 5-10 mm above the well plate to allow room for the degassed coupling gel, as described in step 3.2 (Figure 2A and Figure 1B).

3. Stimulation and neuronal signal acquisition

1. Set the FUS parameters on the TPO control panel (Table 1).
2. Apply the coupling gel on top of the parafilm, and lower the FUS transducer into the coupling gel, ensuring contact with the gel with minimal air bubbles (Figure 1A).
3. Start the MEA system recording by clicking on the Start button on the user interface.
4. Start the FUS sonication by pressing the bottom right button on the TPO (Figure 2A, Label 7), and wait at least 5 min between each round of sonication to allow the neurons to return to a baseline state.
5. Use the trigger pulse generated by the FUS system to align the FUS stimulation sequence to the MEA recording (Figure 1B, Connection 3).

Table 1: Focused ultrasound (FUS) parameters set on the TPO

Parameter	Value
Max Power/Ch	1.200 W
Pactual	0.749 W/channel
ISPPA	10.79 W/cm2
ISPTA	0.05 W/cm2
Burst Length	0.100 ms
Frequency	250.00 kHz
Focus	39.800 mm
Period	20.000 ms
Timer	60.000 s

Resultaten

Figure 1: FUS neuromodulation with a multi-well microelectrode array (MEA). (A) Schematic of the setup for FUS neuromodulation with a multi-well MEA. The acoustic waves generated by the FUS transducer propagate through an FUS cone fill...

Materialen

Lijst van materialen gebruikt in dit artikel

Naam	Bedrijf	Catalogusnummer	Opmerkingen
MEA System	Axion Biosystem Inc.	Maestro Edge	Sampling Rate: 11500 Hz
MEA Plate	Axion Biosystem Inc.	CytoView MEA	Electrode and Well: 16 electrodes in 24 wells
Well plate Interface	Amcor Inc.	Parafilm PM996; P7793	Thickness: 127 µm
CO2 Tank and Regulator for culture	AirGas Inc./ Harris Inc.	9296NC	Concentration: 5%
Culture Media	ThermoFisher Inc.	Laminin; 23017-015	Concentration: 1 µg/mL
HiPSC Neurons	Peprotech	CIPS and GM01582 Derived; 450-10	Concentration: 10 ng/mL (Refer Taga et al [2021]13)
Transducer	Sonic Concepts Inc.	CTX250; 008	Center Frequency: 250 kHz
Matching Network	Sonic Concepts Inc.	CTX250; NFS102v2	Impedance: 50 Ω
Transducer Power Output (TPO)	Sonic Concepts Inc.	Version 4.1; 020	Frequency: From 250 kHz to 2.5 MHz
Membrane	McMaster Inc.	Silicone Rubber; 5542N115	Thickness: 0.0127 cm
Coupling Gel	Parker Laboratory Inc.	Aquasonic 100; B08DDWG GXB	Viscosity: 130,000–185,000 cops
Connection to Probe holder	McMaster Inc.	Steal Threaded Rod; 90322A661	Length: 1–1/2" Long
Hydrophone	Sonic Concepts Inc.	Y-104; 009	Range: 50 kHz–1.9 MHz
Water Tank	Sonic Concepts Inc.	WT	Size: 30 cm x 30 cm x 30 cm
Water Conditioning Unit	Sonic Concepts Inc.	WCU; SN006	Flow Velocity: 50 mL/s maximum
Oscilloscope	Rohde-Schwarz Inc.	RTC1002	Sampling rate: Up to 50 MHz
Stage	Sonic Concepts Inc.	MicroStage; 2	Accuracy: 1 µm
Thermochromic sheet	TIPTEMP Inc.	Liquid Crystal Sheet; TLCSEN337	Range: 22–24 °C
Computer	Microsoft Surface	Surface Pro	CPU i5 1035G4: 3.7 GHz
Data Transfer Software	Mathworks Inc.	MATLAB	Version 2021b
Processing Software	Python Software Foundation	Python	Version 3.7.10