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Topic: patch clamp electrophysiology

ePoster
3 ePosters

In Neuroscience

Comparative transcriptome profiling of multiple human induced pluripotent stem cell-derived sensory neuron populations and functional validation of pain targets on automated patch clamp systems

Vincent Truong, Aaron Randolph, Irene Lu, Rita Cerone, Alison Obergrussberger, Rodolfo Haedo, Tim Strassmaier, Patrick Walsh · FENS Forum 2024

Nociceptors are a subset of sensory neurons that relay painful stimuli from the peripheral tissues. Multiple nociceptor subtypes exist and can respond to different thermal, mechanical, or chemical noxious stimuli. Recent findings with transcriptomics have identified gene expression patterns that classify these sub-types by different ion channels including NaV1.7, NaV1.8, NaV1.9, TRPV1, TRPA1, P2X3, HCN and a number of others that have been implicated in pain. In this study, we have identified a method to rapidly generate a novel TRPA1+ human induced pluripotent stem cell (hiPSC)-derived sensor

ePoster · Neuroscience

Intrinsic electrophysiological features of neurons in the lateral prefrontal and primary visual cortex of the common marmoset

Michael Feyerabend, Stefan Pommer, Michelle Jimenez, Sam Mestern, Jennifer Rachel, Julia Sunstrum, Felix Preuss, Stefan Everling, David Lewis, Guillermo Gonzalez-Burgos, Andreas Neef, Jochen Staiger, Wataru Inoue, Julio Martinez-Trujillo · FENS Forum 2024

Higher-order mental representations underlying working memory function, are believed to arise in primates, with the development and expansion of the granular prefrontal cortex (PFC). For example, in vivo extracellular recordings from behaving non-human primates (NHPs) have shown that persistent firing representing the contents of working memory can be found in lateral PFC but is absent in early sensory areas such as primary visual (V1) cortex. However, the mechanistic basis of potentially unique primate PFC circuitry remains speculative, partly due to the lack of data on the biophysical and m

ePoster · Neuroscience

Understanding the synaptic basis of dystonia pathogenesis triggered by RIMBP1 mutations

Chiara Olmeo, Joaquin Campos, Niccolò Mencacci, Jule Truberg, Moritz Mall, Claudio Acuna · FENS Forum 2024

Dystonia is a debilitating movement disorder characterized by abnormal movements and postures. Given the absence of structural lesions in the brain of most dystonic patients, disruption of synaptic function has been long hypothesized to play a pivotal role in dystonia pathogenesis. We recently identified homozygous frameshift, nonsense, and missense variants in TSPOAP1, the gene encoding active zone RIM-binding protein 1 (RIMBP1), as a novel genetic cause of autosomal recessive dystonia (Mencacci et al., JCI, 2021). RIMBP1 is a presynaptic protein that localizes voltage-gated Ca2+ channels (VG

ePoster · Neuroscience