12 well mea plates with 64 electrodes per well  (Axion BioSystems)

Journal: Scientific Reports

Article Title: Chronic Electrical Stimulation Promotes the Excitability and Plasticity of ESC-derived Neurons following Glutamate-induced Inhibition In vitro

doi: 10.1038/s41598-018-29069-3

Figure Lengend Snippet: ESC-derived neurons and glia form functional neural network on MEA. ( A ) Experimental schedule for neural stem cell seeding and culture. For the control group, recordings were performed from week1 to week 3. ( B ) Representative micro-electrode array (MEA) recording setup. Schematic of the bottom of the well with 4 reference electrodes and 8 × 8 electrode array (left). Top left quadrant of a 64-channel MEA plate, 2 weeks after stem cells seeding (right; Scale = 100 μm). ( C ) Scatter distribution of the spike width (µsec; x-axis) against the peak-to-valley amplitude (µVolt; y-axis) for individual unit recorded from control condition at week 3. The distribution (cell count per bin) is displayed as a projection of each axis. The dashed black line represents the average of spike width (vertical) and peak-to-valley amplitude (horizontal). ( D ) Representative average spike wave forms obtained from 3 electrodes at week 3 from the control group. Data is shown as mean and s.e.m. ( E ) Raster plot of one well recorded at week 3 (top panel). The population instantaneous firing rate (left y-axis in green; wMFR, spikes/bin/electrode) and the percentage of active electrodes per bin (right y-axis, in red; active electrode in %). The vertical dashed and dotted lines indicate the start and stop of a detected population burst, respectively. ( F ) Heat map showing the evolution of the average activity in a control well from week 2 to week 3.

Article Snippet: Briefly, each well of 12 well/64 electrode per well containing MEA plates (Axion Biosystems, GA), or glass bottom petri dishes (Cellvis, CA) were coated with polyethylenimine (PEI) (Sigma-Aldrich, MO) and incubated for 1 h at 37 °C and 5% CO 2 , then washed with deionized water and allowed to air dry overnight.

Techniques: Derivative Assay, Functional Assay, Control, Cell Counting, Activity Assay

Journal: Scientific Reports

Article Title: Chronic Electrical Stimulation Promotes the Excitability and Plasticity of ESC-derived Neurons following Glutamate-induced Inhibition In vitro

doi: 10.1038/s41598-018-29069-3

Figure Lengend Snippet: Acute L-glutamate treatment impaired network activity and synchrony immediately and over a week post-administration. ( A ) Experimental schedule for ESC-derived neuron seeding, culture and L-glutamate treatment. In the treatment group, 100 µM of L-glutamate was administered at day14 for 20 min then washed out. MEA recordings were performed from week 1 to week 3. ( B ) Scatter distribution of the mean burst firing rate (mBR; Burst event/min; x-axis) against the mean firing rate (mFR; log of spike/sec; y-axis) for individual unit recorded from CTR (black filled circles) and L-glut (black open circle) groups. Data is shown for week 2 (left panel) and week 3 (right panel). The normalized distribution CTR (black line) and L-glut (gray line) groups are displayed as a projection of each axis. The dashed black line represents the average for the CTR group. The dotted black line represents the average for the L-glut group. mFR: mean firing rate for individual electrodes; mBR: mean bursting rate for individual electrodes. ( C ) ESC-derived neurons after L-glutamate treatment (L-glut; 100 µM for 20 min at day 14) at week 2 (top panels) and week 3 (bottom panels). From left to right panels are shown SOX-1, βIII-Tubulin and merged image of both fluorescent markers. Scale = 200 μm. ( D ) Change at week 2 and week 3 (expressed as a Z-score from week1 baseline) of the number of bursting cells (left panel) and weighted mean firing rate (wMFR; right panel). For each group, the number of wells with significantly increasing change over the total number of wells recorded is shown above the scatter plot. wMFR: weighted mean population firing rate. ( E ) Change in network synchrony at week 2 and week 3 (expressed as a Z-score from week1 baseline) for event synchronization (left panel), cross-correlation peak (middle panel) and mean network burst firing rate (mBFR; right panel). For each group, the number of wells with significantly increasing change over the total number of wells recorded is shown above the scatter plot. For post-hoc two-sample test *, ** and *** indicate p < 0.05, p < 0.01 and p < 0.001, respectively. mBFR: mean population burst firing rate.

Article Snippet: Briefly, each well of 12 well/64 electrode per well containing MEA plates (Axion Biosystems, GA), or glass bottom petri dishes (Cellvis, CA) were coated with polyethylenimine (PEI) (Sigma-Aldrich, MO) and incubated for 1 h at 37 °C and 5% CO 2 , then washed with deionized water and allowed to air dry overnight.

Techniques: Activity Assay, Derivative Assay

Journal: Scientific Reports

Article Title: Chronic Electrical Stimulation Promotes the Excitability and Plasticity of ESC-derived Neurons following Glutamate-induced Inhibition In vitro

doi: 10.1038/s41598-018-29069-3

Figure Lengend Snippet: DCS and LFS stimulation enhanced the maturation in excitability and neural synchrony following acute L-glutamate treatment. ( A ) Experimental schedule for ESC-derived neuron seeding, culture and treatment. L-glutamate (100 µM) was administered at day14 for 20 min then washed out. LFS was administered from day 15 to day 19 using 10 µA at 0.1 Hz, 15 min/day. DCS was administered in two phases: day14 a cathodal stimulation was performed for 15 min; from day 15 to day 19, anodal stimulation was administered for 15 min per day. Recording was performed on day 14 (week 2) and day 21 (week 3). ( B ) Schematic set up for electrical stimulation on MEA plate. LFS stimulation (10 µA, 0.1 Hz, 15 min/day) was delivered through the MEA electrode using the Maestro system. Four stainless screws were positioned above the MEA cultured neurons and were used to deliver a controlled current (DCS: single-time 10 µA monophonic cathodal 15 min and daily 10 µA monophonic anodal current, 15 min/day) using a custom battery-powered system. ( C ) Change at week 3 (expressed as a Z-score from week1 baseline) of the number of bursting cells (left panel) and wMFR (right panel). For post-hoc multiple comparison using Dunn-Sidak correction *, ** and *** indicate p < 0.05, p < 0.01 and p < 0.001, respectively. wMFR: weighted mean population firing rate. ( D ) Change at week 3 (expressed as a Z-score from week1 baseline) of the event synchronization (left panel), cross-correlation peak (middle panel) and mBFR (right panel). For post-hoc multiple comparison using Dunn-Sidak correction *, ** and *** indicate p < 0.05, p < 0.01 and p < 0.001, respectively. mBFR: mean population burst firing rate.

Article Snippet: Briefly, each well of 12 well/64 electrode per well containing MEA plates (Axion Biosystems, GA), or glass bottom petri dishes (Cellvis, CA) were coated with polyethylenimine (PEI) (Sigma-Aldrich, MO) and incubated for 1 h at 37 °C and 5% CO 2 , then washed with deionized water and allowed to air dry overnight.

Techniques: Derivative Assay, Cell Culture, Battery, Comparison