| Literature DB >> 25505312 |
Takumi Fujita1, Michael J Chen2, Baoman Li2, Nathan A Smith2, Weiguo Peng2, Wei Sun2, Michael J Toner2, Benjamin T Kress2, Linhui Wang2, Abdellatif Benraiss2, Takahiro Takano2, Su Wang2, Maiken Nedergaard1.
Abstract
Experimental advances in the study of neuroglia signaling have been greatly accelerated by the generation of transgenic mouse models. In particular, an elegant manipulation that interferes with astrocyte vesicular release of gliotransmitters via overexpression of a dominant-negative domain of vesicular SNARE (dnSNARE) has led to documented astrocytic involvement in processes that were traditionally considered strictly neuronal, including the sleep-wake cycle, LTP, cognition, cortical slow waves, depression, and pain. A key premise leading to these conclusions was that expression of the dnSNARE was specific to astrocytes. Inconsistent with this premise, we report here widespread expression of the dnSNARE transgene in cortical neurons. We further demonstrate that the activity of cortical neurons is reversibly suppressed in dnSNARE mice. These findings highlight the need for independent validation of astrocytic functions identified in dnSNARE mice and thus question critical evidence that astrocytes contribute to neurotransmission through SNARE-dependent vesicular release of gliotransmitters.Entities:
Keywords: EEG; GFAP; SNARE; adenosine; sleep
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Year: 2014 PMID: 25505312 PMCID: PMC4261088 DOI: 10.1523/JNEUROSCI.2585-14.2014
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167