Abstract
This review article aims to give a brief summary on the novel technologies, the challenges, our current understanding, and the open questions in the field of the neurophysiology of the developing cerebral cortex in rodents. In the past, in vitro electrophysiological and calcium imaging studies on single neurons provided important insights into the function of cellular and subcellular mechanism during early postnatal development. In the past decade, neuronal activity in large cortical networks was recorded in pre- and neonatal rodents in vivo by the use of novel high-density multi-electrode arrays and genetically encoded calcium indicators. These studies demonstrated a surprisingly rich repertoire of spontaneous cortical and subcortical activity patterns, which are currently not completely understood in their functional roles in early development and their impact on cortical maturation. Technological progress in targeted genetic manipulations, optogenetics, and chemogenetics now allow the experimental manipulation of specific neuronal cell types to elucidate the function of early (transient) cortical circuits and their role in the generation of spontaneous and sensory evoked cortical activity patterns. Large-scale interactions between different cortical areas and subcortical regions, characterization of developmental shifts from synchronized to desynchronized activity patterns, identification of transient circuits and hub neurons, role of electrical activity in the control of glial cell differentiation and function are future key tasks to gain further insights into the neurophysiology of the developing cerebral cortex.
Highlights
WHAT ARE OUR TOOLS?In the last decade life sciences has shown a tremendous progress in developing and improving novel technologies
In cellular neurophysiology classical electrophysiological recording techniques and cellular imaging methods are very successfully combined with new tools in molecular biology and genetics to gain deeper insights into the function of single neurons and defined neuronal networks
Using the powerful Patch-seq technique, whole-cell patch-clamp recordings can be combined with morphological reconstructions, immunohistochemistry, and single-cell RNA-sequencing to perform a multidimensional characterization of a single cell and to correlate the gene expression profile with its structural and functional properties (Cadwell et al, 2017; Scala et al, 2021)
Summary
WHAT ARE OUR TOOLS?In the last decade life sciences has shown a tremendous progress in developing and improving novel technologies. In vitro electrophysiological and calcium imaging studies on single neurons provided important insights into the function of cellular and subcellular mechanism during early postnatal development.
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