2023
DOI: 10.1002/glia.24384
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Astrocytic A2A receptors silencing negatively impacts hippocampal synaptic plasticity and memory of adult mice

Abstract: Astrocytes are wired to bidirectionally communicate with neurons namely with synapses, thus shaping synaptic plasticity, which in the hippocampus is considered to underlie learning and memory. Adenosine A 2A receptors (A 2A R) are a potential candidate to modulate this bidirectional communication, since A 2A R regulate synaptic plastic-

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Cited by 3 publications
(9 citation statements)
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“…This A 2A R-mediated control of AD-related dysfunction involves an overfunction of neuronal A 2A R [ 25 , 31 , 67 ], in accordance with the predominant localization of A 2A R in excitatory synapses in the limbic cortex [ 68 , 69 ]. However, A 2A R are also present in astrocytes and the selective manipulation of astrocytic A 2A R has an impact on memory function [ 23 , 29 , 70 ]. Furthermore, A 2A R modulate alterations triggered by Aβ in primary cultures of astrocytes, namely decreased glutamate uptake [ 21 ], altered Ca 2+ dynamics [ 22 ], and increased hemichannel activity and subsequently ATP release [ 20 ], a danger signal in brain disease conditions [ 71 ].…”
Section: Discussionmentioning
confidence: 99%
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“…This A 2A R-mediated control of AD-related dysfunction involves an overfunction of neuronal A 2A R [ 25 , 31 , 67 ], in accordance with the predominant localization of A 2A R in excitatory synapses in the limbic cortex [ 68 , 69 ]. However, A 2A R are also present in astrocytes and the selective manipulation of astrocytic A 2A R has an impact on memory function [ 23 , 29 , 70 ]. Furthermore, A 2A R modulate alterations triggered by Aβ in primary cultures of astrocytes, namely decreased glutamate uptake [ 21 ], altered Ca 2+ dynamics [ 22 ], and increased hemichannel activity and subsequently ATP release [ 20 ], a danger signal in brain disease conditions [ 71 ].…”
Section: Discussionmentioning
confidence: 99%
“…The selective deletion of A 2A R in astrocytes was accomplished in A 2A R floxed (A 2A flox/flox ) mice through the Cre-lox method. Briefly, an AAV5-GFAP-GFP-CRE viral construct (1 µL from 4.8 × 10 12 particles/mL, obtained from Vector Core, University of North Carolina, USA) was bilaterally administrated into the CA1 region of the dorsal hippocampus (GFAP-CRE-A 2A R mice), whereas control (GFAP-CTR) mice received a similar construct without Cre recombinase, AAV5-GFAP-eGFP (Vector Core, University of North Carolina, USA), as previously described [ 23 ].…”
Section: Methodsmentioning
confidence: 99%
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