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Journal ArticleDOI

Local Ca2+ detection and modulation of synaptic release by astrocytes

TLDR
Evidence is provided that astrocytes are integrated in local synaptic functioning in adult brain through GTP- and inositol-1,4,5-trisphosphate–dependent signaling and is relevant for basal synaptic function.
Abstract
Astrocytes communicate with synapses by means of intracellular calcium ([Ca(2+)](i)) elevations, but local calcium dynamics in astrocytic processes have never been thoroughly investigated. By taking advantage of high-resolution two-photon microscopy, we identify the characteristics of local astrocyte calcium activity in the adult mouse hippocampus. Astrocytic processes showed intense activity, triggered by physiological transmission at neighboring synapses. They encoded synchronous synaptic events generated by sparse action potentials into robust regional (∼12 μm) [Ca(2+)](i) elevations. Unexpectedly, they also sensed spontaneous synaptic events, producing highly confined (∼4 μm), fast (millisecond-scale) miniature Ca(2+) responses. This Ca(2+) activity in astrocytic processes is generated through GTP- and inositol-1,4,5-trisphosphate-dependent signaling and is relevant for basal synaptic function. Thus, buffering astrocyte [Ca(2+)](i) or blocking a receptor mediating local astrocyte Ca(2+) signals decreased synaptic transmission reliability in minimal stimulation experiments. These data provide direct evidence that astrocytes are integrated in local synaptic functioning in adult brain.

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Journal ArticleDOI

Spatial organization of neuron–astrocyte interactions in the somatosensory cortex

TL;DR: In this paper , it was shown that CB1R-mediated activation by neuron-released endocannabinoids elevate astrocyte Ca2+ levels, stimulate ATP/adenosine release as gliotransmitters, and transiently depress synaptic transmission in layer 5 pyramidal neurons at relatively distant synapses (˃20 μm) from the stimulated neuron.
Posted ContentDOI

Chronic Gq activation of ventral hippocampal neurons and astrocytes differentially affects memory and behavior

TL;DR: This study provides evidence for how each of these cell types are uniquely engaged in disorders that have characteristic network dysfunction while adding a more direct role for glia in modulating behavior.
Dissertation

Astrocyte control of neurotransmitter signalling

N Bazargani
TL;DR: In this article, a relatively understudied G protein coupled receptor present in astrocytes, GPCR37L1, was found to decrease the activity of glutamate transporters and decrease neuronal NMDA receptor activity.
References
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Journal ArticleDOI

Tripartite synapses: astrocytes process and control synaptic information

TL;DR: There is an emerging view, which is reviewed herein, in which brain function actually arises from the coordinated activity of a network comprising both neurons and glia, rather than the classically accepted paradigm that brain function results exclusively from neuronal activity.
Journal ArticleDOI

Control of synapse number by glia.

TL;DR: It is shown that few synapses form in the absence of glial cells and that the fewsynapses that do form are functionally immature, and that CNS synapse number can be profoundly regulated by nonneuronal signals.
Journal ArticleDOI

Long-term potentiation depends on release of d -serine from astrocytes

TL;DR: It is demonstrated that Ca2+-dependent release of d-serine from an astrocyte controls NMDAR-dependent plasticity in many thousands of excitatory synapses nearby.
Journal ArticleDOI

Definition of the Readily Releasable Pool of Vesicles at Hippocampal Synapses

TL;DR: It is found that hypertonic solutions do not act through changes in intracellular calcium, which means that the synaptic release probability depends on the size of the readily releasable pool.
Journal ArticleDOI

Neuronal Synchrony Mediated by Astrocytic Glutamate through Activation of Extrasynaptic NMDA Receptors

TL;DR: The results reveal a distinct mechanism for neuronal excitation and synchrony and highlight a functional link between astrocytic glutamate and extrasynaptic NMDA receptors.
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