3D Microelectrode Arrays: A New Frontier in Neuroscience
Revolutionizing neuron study with 3D technology for better insights.
João Serra, José C. Mateus, Susana Cardoso, João Ventura, Paulo Aguiar, Diana C. Leitao
― 7 min read
Table of Contents
Microelectrode Arrays (MEAs) are special tools used in science to measure and study the electrical signals from groups of nerve cells, also known as Neurons. Think of them as tiny listening devices that can catch all the chatter happening in a group of neurons, much like how a busy café has a lot of conversations going on at once. These devices are really good at monitoring how neurons communicate with each other and can also send signals back to them. This capability makes MEAs valuable for researching brain disorders like Parkinson’s disease and epilepsy.
What Are Microelectrode Arrays?
MEAs are tiny platforms covered with multiple Electrodes. These electrodes are like microphones but designed specifically to pick up the electrical signals produced by neurons. The exciting part? MEAs can record these signals from living neurons while they are in a dish, allowing scientists to watch how these cells behave in real-time.
Traditionally, these MEAs were two-dimensional, which is similar to reading a book flat on a table. The problem? Neurons in real brains interact in three dimensions, so it's not always easy to understand their behavior when they are stuck on a flat surface. This limitation got researchers scratching their heads and looking for ways to create MEAs that can work in three dimensions.
The Shift to 3D MEAs
Recent developments have shifted the focus from 2D MEAs to 3D versions. Just like building a Lego tower instead of sticking with flat pieces, this new approach allows scientists to study how neurons behave in a space that mimics a living brain more closely. Researchers have come up with fancy designs to create 3D MEAs using techniques inspired by origami. Yes, that’s right! They are using folding techniques similar to those used in making paper cranes.
These new 3D MEAs can be made using special materials that can change shape when heated. These changes allow the electrodes to stand upright instead of lying flat, making it easier to reach the neurons from various angles. This design gives scientists access to a whole new level of data about how neurons share information and react to different conditions.
Building the MEA
The process of making these MEAs is a bit like baking a cake—if baking involved layers of very thin films! The base of the MEA is made of glass, which provides a sturdy foundation. On top of this glass, researchers create several layers, including a sacrificial layer that eventually gets removed, leaving behind only the parts they want to keep.
The electrodes are then made from a combination of metal and special polymers that can bend when needed. This bending is what changes a flat MEA into a 3D version, enabling better interactions with neurons.
To achieve this, scientists use some heat tricks. By carefully controlling the temperature and applying stress to certain layers, they can shape the electrodes into the desired 3D positions. Picture a magician pulling a rabbit out of a hat, except the magician is a scientist, and instead of a rabbit, they're pulling out a 3D electrode!
The Benefits of Using 3D MEAs
The main advantage of moving to 3D MEAs is their ability to study neurons in an environment that more closely resembles their natural habitat. Just like a fish out of water struggles to breathe, neurons also have a tough time acting normally if confined to a flat surface. By using 3D MEAs, researchers can observe how neurons communicate, how they process information, and how they respond to different drugs or therapies in a way that’s much more similar to how they would in a brain.
Furthermore, using flexible materials helps match the mechanical properties of the MEAs to living cells, making them more comfortable and suitable for long-term use. No one likes being poked with a stick, and neither do neurons, so being gentle matters.
How Do Scientists Test the MEAs?
Once the MEAs are fabricated, it’s essential to test them to ensure they work correctly before throwing neurons into the mix. Engineers use various techniques to measure how well the electrodes pick up signals and how much noise there is in the recordings.
Imagine trying to listen to your favorite song on a radio, but there’s lots of static—frustrating, right? Scientists aim to reduce that static to hear the beautiful music of neuron activity instead. They measure the signal levels and ensure everything is operating smoothly before introducing the neurons.
Growing Neurons on MEAs
After testing, it’s time to bring in the stars of the show: the neurons! Scientists typically grow these neurons in a gel-like substance to help them form the necessary connections. They carefully mix the gel with the neurons, ensuring a good spread across the MEA. Think of it as making a neuron smoothie, where the MEA is the blending cup.
The neurons need some time to settle and grow, so scientists incubate the MEAs. The warm environment is perfect for neurons to thrive, similar to how certain plants need specific temperatures to bloom. As the neurons start to establish themselves, they begin to communicate with each other and with the MEAs.
Recording Neuronal Activity
After giving the neurons a little home time, scientists are ready to record their activity. Using the 3D MEAs, they can listen to the neurons firing off electrical signals. This is where the magic happens, as researchers can observe how neurons react to various stimuli, how they communicate with each other, and how they behave in groups.
During these recordings, scientists often notice bursts of activity—like a sudden burst of energy in a classroom when everyone gets excited about a topic! Each electrode can detect these events, letting researchers see how the neurons' signals travel through the 3D space.
Impedance and Noise Levels
To make sure the recordings are clear, the impedance of the electrodes is carefully monitored. Impedance is like the resistance to electrical current. If it’s too high, the quality of the recordings can suffer. Scientists aim for specific impedance ranges to ensure they capture neuron activity without too much noise, much like tuning a guitar before a concert.
They also keep an eye on noise levels to make sure they can hear the neurons well. If there's too much background noise, it’s like trying to hear someone talk while there’s construction happening nearby. The goal is to keep the noise low so that the recorded signals represent true neuronal behavior.
Challenges with 3D MEAs
While the 3D MEAs offer exciting opportunities, they come with their own set of challenges. One major hurdle is ensuring that all electrodes are functional. Sometimes, due to small errors in the fabrication process, not all electrodes work as intended. Scientists strive to improve the fabrication techniques, much like chefs refining a recipe for the perfect cookie.
Another challenge is the long-term stability of the MEAs once they are introduced to the living environment. After some time in use, it’s important to check that the electrodes still perform well and remain free of damage.
Future of 3D MEAs
Looking ahead, the possibilities for 3D MEAs are vast. Researchers can explore new electroactive systems, such as heart cells or muscle tissues, using these devices. The flexibility and adaptability of 3D MEAs also open doors for future technologies, including incorporation into microfluidic platforms, which can enhance overall studies.
Moreover, as researchers improve fabrication techniques, they may be able to create MEAs with more customized shapes and designs. This way, the electrodes can be better tailored to specific applications. Imagine being able to create your own custom smartphone case or gadget—this is what scientists are working towards for their MEAs.
Conclusion
Microelectrode Arrays are paving the way for exciting discoveries in neuroscience. By transitioning from 2D to intricate 3D designs, researchers are now able to observe the electrical activity of neurons with greater accuracy and relevance to real-life scenarios. As technology advances, these tools will continue to play a key role in understanding brain function and developing treatments for neurological disorders.
So, the next time you hear about MEAs, picture tiny devices that are not just recording electrical signals but are also helping scientists unlock the secrets of the brain, one neuron at a time—no magic wand required!
Original Source
Title: Stress-actuated Flexible Microelectrode Arrays for Activity Recording in 3D Neuronal Cultures
Abstract: Microelectrode arrays (MEAs) are instrumental in monitoring electrogenic cell populations, such as neuronal cultures, allowing high precision measurements of electrical activity. Although three-dimensional neuronal cultures replicate the behavior of in vivo systems better than two-dimensional models, conventional planar MEAs are not well suited to capture activity within such networks. Novel MEA geometries can overcome this difficulty, but often at the cost of increased fabrication complexity. Here, we used the stress mismatch between thin film layers to fabricate MEAs with vertical electrodes, using methods compatible with established microfabrication protocols. A micrometric SiO2 hinge enables control over the bending angle of flexible polyimide structures with embedded electrodes. The performance of the patterned electrodes was assessed before and after stress actuation, through impedance measurements, voltage noise mapping, and neuronal activity recordings. 3D MEAs with 30x30 {micro}m2 electrodes showed an impedance of 0.96 {+/-} 0.07 M{Omega} per electrode and detected neuronal activity spikes with amplitudes as high as 400 {micro}V. These results demonstrate the potential of the developed methods to provide a scalable approach to fabricate 3D MEAs, enabling enhanced recording capabilities for in vitro neuronal cultures.
Authors: João Serra, José C. Mateus, Susana Cardoso, João Ventura, Paulo Aguiar, Diana C. Leitao
Last Update: 2024-12-17 00:00:00
Language: English
Source URL: https://www.biorxiv.org/content/10.1101/2024.12.12.628189
Source PDF: https://www.biorxiv.org/content/10.1101/2024.12.12.628189.full.pdf
Licence: https://creativecommons.org/licenses/by-nc/4.0/
Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.
Thank you to biorxiv for use of its open access interoperability.