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Journal ArticleDOI

Astroglial metabolic networks sustain hippocampal synaptic transmission.

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TLDR
It is shown that the gap-junction subunit proteins connexin 43 and 30 allow intercellular trafficking of glucose and its metabolites through astroglial networks for the delivery of energetic metabolites from blood vessels to distal neurons.
Abstract
Astrocytes provide metabolic substrates to neurons in an activity-dependent manner. However, the molecular mechanisms involved in this function, as well as its role in synaptic transmission, remain unclear. Here, we show that the gap-junction subunit proteins connexin 43 and 30 allow intercellular trafficking of glucose and its metabolites through astroglial networks. This trafficking is regulated by glutamatergic synaptic activity mediated by AMPA receptors. In the absence of extracellular glucose, the delivery of glucose or lactate to astrocytes sustains glutamatergic synaptic transmission and epileptiform activity only when they are connected by gap junctions. These results indicate that astroglial gap junctions provide an activity-dependent intercellular pathway for the delivery of energetic metabolites from blood vessels to distal neurons.

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Astrocytes: biology and pathology

TL;DR: Astrocyte functions in healthy CNS, mechanisms and functions of reactive astrogliosis and glial scar formation, and ways in which reactive astrocytes may cause or contribute to specific CNS disorders and lesions are reviewed.
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Molecular dissection of reactive astrogliosis and glial scar formation.

TL;DR: Developments in the signaling mechanisms that regulate specific aspects of reactive astrogliosis are reviewed and the potential to identify novel therapeutic molecular targets for diverse neurological disorders is highlighted.
Journal ArticleDOI

Brain energy metabolism: focus on astrocyte-neuron metabolic cooperation

TL;DR: This review focuses on the cellular aspects of brain energy metabolism, with a particular emphasis on the metabolic interactions between neurons and astrocytes.
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Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation

TL;DR: It is concluded that astrocyte-neuron lactate transport is required for long-term memory formation, suggesting that lactate import into neurons is necessary for long -term memory.
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.
References
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Journal ArticleDOI

Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization

TL;DR: It is reported that glutamate, in addition to its receptor-mediated actions on neuronal excitability, stimulates glycolysis--i.e., glucose utilization and lactate production--in astrocytes and is consistent with data obtained from functional brain imaging studies indicating local nonoxidative glucose utilization during physiological activation.
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Metabolic coupling between glia and neurons

TL;DR: The aim of this review was to establish a chronology of events leading to and following the publication of the LNDC-REVIEW in 1996.
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An astrocytic basis of epilepsy

TL;DR: It is reported that paroxysmal depolarization shifts can be initiated by release of glutamate from extrasynaptic sources or by photolysis of caged Ca2+ in astrocytes, and this finding identifies astroCytes as a proximal target for the treatment of epileptic disorders.
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Signaling at the Gliovascular Interface

TL;DR: Astrocytic end-foot processes plastered at the vessel wall as a center for purinergic signaling is identified, speculated that calcium signaling may play a role in astrocyic functions related to the blood-brain barrier, including blood flow regulation, metabolic trafficking, and water homeostasis.
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Segregated expression of AMPA-type glutamate receptors and glutamate transporters defines distinct astrocyte populations in the mouse hippocampus.

TL;DR: The observed heterogeneity of cells with GFAP promoter-regulated EGFP expression and S100β/GFAP immunoreactivity challenges the hitherto accepted definition of astrocytes.
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