Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo

Although astrocytes are the most abundant cell type in the brain, evidence for their activation during physiological sensory activity is lacking. Here we show that whisker stimulation evokes increases in astrocytic cytosolic calcium (Ca 2+ ) within the barrel cortex of adult mice. Increases in astro...

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Veröffentlicht in:Nature neuroscience 2006-06, Vol.9 (6), p.816-823
Hauptverfasser: Wang, Xiaohai, Lou, Nanhong, Xu, Qiwu, Tian, Guo-Feng, Peng, Wei Guo, Han, Xiaoning, Kang, Jian, Takano, Takahiro, Nedergaard, Maiken
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container_end_page 823
container_issue 6
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container_title Nature neuroscience
container_volume 9
creator Wang, Xiaohai
Lou, Nanhong
Xu, Qiwu
Tian, Guo-Feng
Peng, Wei Guo
Han, Xiaoning
Kang, Jian
Takano, Takahiro
Nedergaard, Maiken
description Although astrocytes are the most abundant cell type in the brain, evidence for their activation during physiological sensory activity is lacking. Here we show that whisker stimulation evokes increases in astrocytic cytosolic calcium (Ca 2+ ) within the barrel cortex of adult mice. Increases in astrocytic Ca 2+ were a function of the frequency of stimulation, occurred within several seconds and were inhibited by metabotropic glutamate receptor antagonists. To distinguish between synaptic input and output, local synaptic activity in cortical layer 2 was silenced by iontophoresis of AMPA and NMDA receptor antagonists. The antagonists did not reduce astrocytic Ca 2+ responses despite a marked reduction in excitatory postsynaptic currents in response to whisker stimulation. These findings indicate that astrocytes respond to synaptic input, by means of spillover or ectopic release of glutamate, and that increases in astrocytic Ca 2+ occur independently of postsynaptic excitatory activity.
doi_str_mv 10.1038/nn1703
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Here we show that whisker stimulation evokes increases in astrocytic cytosolic calcium (Ca 2+ ) within the barrel cortex of adult mice. Increases in astrocytic Ca 2+ were a function of the frequency of stimulation, occurred within several seconds and were inhibited by metabotropic glutamate receptor antagonists. To distinguish between synaptic input and output, local synaptic activity in cortical layer 2 was silenced by iontophoresis of AMPA and NMDA receptor antagonists. The antagonists did not reduce astrocytic Ca 2+ responses despite a marked reduction in excitatory postsynaptic currents in response to whisker stimulation. 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subjects Adenosine
Afferent Pathways - physiology
Animal Genetics and Genomics
Animals
Astrocytes
Astrocytes - drug effects
Astrocytes - metabolism
Behavioral Sciences
Biological Techniques
Biomedical and Life Sciences
Biomedicine
Calcium - metabolism
Calcium Signaling - drug effects
Calcium Signaling - physiology
Cell Communication - drug effects
Cell Communication - physiology
Central nervous system
Electrodes
Excitatory Amino Acid Antagonists - pharmacology
Excitatory Postsynaptic Potentials - drug effects
Excitatory Postsynaptic Potentials - physiology
Female
Male
Mechanoreceptors - physiology
Mice
Neural transmission
Neurobiology
Neurosciences
Physical Stimulation
Physiology
Reaction Time - drug effects
Reaction Time - physiology
Receptors, AMPA - antagonists & inhibitors
Receptors, AMPA - metabolism
Receptors, Metabotropic Glutamate - agonists
Receptors, Metabotropic Glutamate - metabolism
Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
Receptors, N-Methyl-D-Aspartate - metabolism
Regulation
Somatosensory Cortex - cytology
Somatosensory Cortex - physiology
Synaptic Transmission - drug effects
Synaptic Transmission - physiology
Touch - physiology
Up-Regulation - drug effects
Up-Regulation - physiology
Vibrissae - innervation
Vibrissae - physiology
title Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo
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