Abstract
Simultaneously recording network activity and ultrastructural changes of the synapse is essential for advancing our understanding of the basis of neuronal functions. However, the rapid millisecond-scale fluctuations in neuronal activity and the subtle sub-diffraction resolution changes of synaptic morphology pose significant challenges to this endeavour. Here, we use graphene microelectrode arrays (G-MEAs) to address these challenges, as they are compatible with high spatial resolution imaging across various scales as well as high temporal resolution electrophysiological recordings. Furthermore, alongside G-MEAs, we deploy an easy-to-implement machine learning-based algorithm to efficiently process the large datasets collected from MEA recordings. We demonstrate that the combined use of G-MEAs, machine learning (ML)-based spike analysis, and four-dimensional (4D) structured illumination microscopy (SIM) enables the monitoring of the impact of disease progression on hippocampal neurons which have been treated with an intracellular cholesterol transport inhibitor mimicking Niemann-Pick disease type C (NPC) and show that synaptic boutons, compared to untreated controls, significantly increase in size, which leads to a loss in neuronal signalling capacity.
Competing Interest Statement
The authors have declared no competing interest.
Acronyms
- G-MEAs
- Graphene microelectrode arrays
- NPC
- Niemann-Pick disease type C
- MEAs
- Microelectrode arrays
- FOV
- Field of view
- ITO
- Indium tin oxide
- ML
- Machine Learning
- SIM
- Structured illumination microscopy
- DEC
- Deep Embedding for Clustering
- IDEC
- Improved Deep Embedding for Clustering
- AE-Ensemble
- Autoencoder-Ensemble
- Deep AE
- Standard deep autoencoder
- DIV
- Day in vitro
- AAV
- Adeno-associated viruses
- 4D-SIM
- Four-dimensional structured illumination microscopy
- 3D
- Three-dimensional
- FLIM
- Fluorescence lifetime imaging microscopy
- FRET
- Fluorescence resonance energy transfer