期刊
NATURE NEUROSCIENCE
卷 18, 期 3, 页码 423-434出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nn.3930
关键词
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资金
- US National Institutes of Health [AG039220, AR056299, AG034531, HL60664, HL100406, AG022074, N5065780]
- MetLife Foundation Award
- National Center for Research Resources [RR18938]
Astrocytes express a variety of G protein-coupled receptors and might influence cognitive functions, such as learning and memory. However, the roles of astrocytic G(s)-coupled receptors in cognitive function are not known. We found that humans with Alzheimer's disease (AD) had increased levels of the Gs-coupled adenosine receptor A(2A) in astrocytes. Conditional genetic removal of these receptors enhanced long-term memory in young and aging mice and increased the levels of Arc (also known as Arg3.1), an immediate-early gene that is required for long-term memory. Chemogenetic activation of astrocytic G(s)-coupled signaling reduced long-term memory in mice without affecting learning. Like humans with AD, aging mice expressing human amyloid precursor protein (hAPP) showed increased levels of astrocytic A(2A) receptors. Conditional genetic removal of these receptors enhanced memory in aging hAPP mice. Together, these findings establish a regulatory role for astrocytic Gs-coupled receptors in memory and suggest that AD-linked increases in astrocytic A(2A) receptor levels contribute to memory loss.
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