scholarly journals Multielectrode array recordings of human iPSC-derived neurons reveal differences in network activity depending on differentiation protocol and genome modification

Author(s):  
Sandra Fischer ◽  
Frank Gillardon
PLoS ONE ◽  
2017 ◽  
Vol 12 (10) ◽  
pp. e0186147 ◽  
Author(s):  
Benjamin M. Bader ◽  
Anne Steder ◽  
Anders Bue Klein ◽  
Bente Frølund ◽  
Olaf H. U. Schroeder ◽  
...  

2008 ◽  
Vol 174 (2) ◽  
pp. 227-236 ◽  
Author(s):  
Martin D. Haustein ◽  
Thomas Reinert ◽  
Annika Warnatsch ◽  
Bernhard Englitz ◽  
Beatrice Dietz ◽  
...  

2017 ◽  
Author(s):  
Daniel J. O'Shea ◽  
Krishna V. Shenoy

Electrical stimulation is a widely used and effective tool in systems neuroscience, neural prosthetics, and clinical neurostimulation. However, electrical artifacts evoked by stimulation significantly complicate the detection of spiking activity on nearby recording electrodes. Here, we present ERAASR: an algorithm for Estimation and Removal of Artifacts on Arrays via Sequential principal components Regression. This approach leverages the similar structure of artifact transients, but not spiking activity, across simultaneously recorded channels on the array, across pulses within a train, and across trials. The effectiveness of the algorithm is demonstrated in macaque dorsal premotor cortex using acute linear multielectrode array recordings and single electrode stimulation. Large electrical artifacts appeared on all channels during stimulation. After application of ERAASR, the cleaned signals were quiescent on channels with no spontaneous spiking activity, whereas spontaneously active channels exhibited evoked spikes which closely resembled spontaneously occurring spiking waveforms. The ERAASR algorithm requires no special hardware and comprises sequential application of straightforward linear methods with intuitive parameters. Enabling simultaneous electrical stimulation and multielectrode array recording can help elucidate the causal links between neural activity and cognitive functions and enable the design and implementation of novel sensory protheses.


Author(s):  
Satarupa Biswas ◽  
Rinku Roy ◽  
Debdeep Sikdar ◽  
Soumen Das ◽  
Manjunatha Mahadevappa

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Maria Sundberg ◽  
Hannah Pinson ◽  
Richard S. Smith ◽  
Kellen D. Winden ◽  
Pooja Venugopal ◽  
...  

AbstractReciprocal copy number variations (CNVs) of 16p11.2 are associated with a wide spectrum of neuropsychiatric and neurodevelopmental disorders. Here, we use human induced pluripotent stem cells (iPSCs)-derived dopaminergic (DA) neurons carrying CNVs of 16p11.2 duplication (16pdup) and 16p11.2 deletion (16pdel), engineered using CRISPR-Cas9. We show that 16pdel iPSC-derived DA neurons have increased soma size and synaptic marker expression compared to isogenic control lines, while 16pdup iPSC-derived DA neurons show deficits in neuronal differentiation and reduced synaptic marker expression. The 16pdel iPSC-derived DA neurons have impaired neurophysiological properties. The 16pdel iPSC-derived DA neuronal networks are hyperactive and have increased bursting in culture compared to controls. We also show that the expression of RHOA is increased in the 16pdel iPSC-derived DA neurons and that treatment with a specific RHOA-inhibitor, Rhosin, rescues the network activity of the 16pdel iPSC-derived DA neurons. Our data suggest that 16p11.2 deletion-associated iPSC-derived DA neuron hyperactivation can be rescued by RHOA inhibition.


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