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GABABreceptors mediate intracellular calcium release in astrocytes of the prefrontal cortex

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AbstractThe prefrontal cortex (PFC) is a cortical brain region whose multifaceted functions are based on a complex interplay between excitatory pyramidal neurons, inhibitory GABAergic interneurons and astrocytes maintaining a fine-tuned excitation/inhibition balance (E/I balance). The regulation of the E/I balance in cortical network is crucial as the disruption leads to impairments in PFC-associated behavior and pathologies. Astrocytes express specific GABA receptors that mediate intracellular Ca2+signaling upon stimulation by γ-aminobutyric acid (GABA), resulting in the release of gliotransmitters directly impacting information processing. However, the signaling pathway leading to GABA-induced Ca2+signaling in astrocytes of the PFC is not well understood. Here we took advantage of GLAST-promoter driven GCaMP6s expression in astrocytes to study GABAergic Ca2+signaling in PFC astrocytes by confocal microscopy. The results show that GABA induces Ca2+signaling via the stimulation of the metabotropic GABABreceptor in astrocytes. GABABreceptor-mediated Ca2+signals greatly depend on intracellular Ca2+stores rather than on extracellular Ca2+. Additionally, antagonists of the PLC/IP3-signaling cascade significantly reduced GABABreceptor-mediated Ca2+signaling in astrocytes, suggesting that astrocytic GABABreceptors in the PFC are coupled to the Gq-GPCR signaling pathway.
Title: GABABreceptors mediate intracellular calcium release in astrocytes of the prefrontal cortex
Description:
AbstractThe prefrontal cortex (PFC) is a cortical brain region whose multifaceted functions are based on a complex interplay between excitatory pyramidal neurons, inhibitory GABAergic interneurons and astrocytes maintaining a fine-tuned excitation/inhibition balance (E/I balance).
The regulation of the E/I balance in cortical network is crucial as the disruption leads to impairments in PFC-associated behavior and pathologies.
Astrocytes express specific GABA receptors that mediate intracellular Ca2+signaling upon stimulation by γ-aminobutyric acid (GABA), resulting in the release of gliotransmitters directly impacting information processing.
However, the signaling pathway leading to GABA-induced Ca2+signaling in astrocytes of the PFC is not well understood.
Here we took advantage of GLAST-promoter driven GCaMP6s expression in astrocytes to study GABAergic Ca2+signaling in PFC astrocytes by confocal microscopy.
The results show that GABA induces Ca2+signaling via the stimulation of the metabotropic GABABreceptor in astrocytes.
GABABreceptor-mediated Ca2+signals greatly depend on intracellular Ca2+stores rather than on extracellular Ca2+.
Additionally, antagonists of the PLC/IP3-signaling cascade significantly reduced GABABreceptor-mediated Ca2+signaling in astrocytes, suggesting that astrocytic GABABreceptors in the PFC are coupled to the Gq-GPCR signaling pathway.

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