4.6 Article

Neuronal Activity Patterns Regulate Brain-Derived Neurotrophic Factor Expression in Cortical Cells via Neuronal Circuits

Journal

FRONTIERS IN NEUROSCIENCE
Volume 15, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2021.699583

Keywords

activity dependence; promoter activity; gene expression; BDNF; cortex; organotypic culture; live imaging; calcium signaling

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During development, physiological neuronal activity modulates the expression of wiring molecules by altering gene expression in cortical circuits. The study showed that patterned stimuli regulated BDNF promoter activity differently in upper layer neurons, with increases in promoter activity roughly proportional to the increase in intracellular Ca2+ concentration per unit time. These results suggest that physiological stimulation patterns tune activity-dependent gene expression in developing cortical neurons via cortical circuits and altering intracellular calcium signaling.
During development, cortical circuits are remodeled by spontaneous and sensory-evoked activity via alteration of the expression of wiring molecules. An intriguing question is how physiological neuronal activity modifies the expression of these molecules in developing cortical networks. Here, we addressed this issue, focusing on brain-derived neurotrophic factor (BDNF), one of the factors underlying cortical wiring. Real-time imaging of BDNF promoter activity in organotypic slice cultures revealed that patterned stimuli differentially regulated the increase and the time course of the promoter activity in upper layer neurons. Calcium imaging further demonstrated that stimulus-dependent increases in the promoter activity were roughly proportional to the increase in intracellular Ca2+ concentration per unit time. Finally, optogenetic stimulation showed that the promoter activity was increased efficiently by patterned stimulation in defined cortical circuits. These results suggest that physiological stimulation patterns differentially tune activity-dependent gene expression in developing cortical neurons via cortical circuits, synaptic responses, and alteration of intracellular calcium signaling.

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