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J Neurosci. 2014 Apr 23;34(17):6107-11. doi: 10.1523/JNEUROSCI.3762-13.2014.

Mice with compromised 5-HTT function lack phosphotyrosine-mediated inhibitory control over prefrontal 5-HT responses.

Author information

1
Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada, Department of Psychiatry, Columbia University, New York, New York 10032, and Department of Obstetrics and Gynaecology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

Abstract

The activity of the prefrontal cortex is essential for normal emotional processing and is strongly modulated by serotonin (5-HT). Yet, little is known about the regulatory mechanisms that control the activity of the prefrontal 5-HT receptors. Here, we found and characterized a deregulation of prefrontal 5-HT receptor electrophysiological signaling in mouse models of disrupted serotonin transporter (5-HTT) function, a risk factor for emotional and cognitive disturbances. We identified a novel tyrosine kinase-dependent mechanism that regulates 5-HT-mediated inhibition of prefrontal pyramidal neurons. We report that mice with compromised 5-HTT, resulting from either genetic deletion or brief treatment with selective serotonin reuptake inhibitors during development, have amplified 5-HT1A receptor-mediated currents in adulthood. These greater inhibitory effects of 5-HT are accompanied by enhanced downstream coupling to Kir3 channels. Notably, in normal wild-type mice, we found that these larger 5-HT1A responses can be mimicked through inhibition of Src family tyrosine kinases. By comparison, in our 5-HTT mouse models, the larger 5-HT1A responses were rapidly reduced through inhibition of tyrosine phosphatases. Our findings implicate tyrosine phosphorylation in regulating the electrophysiological effects of prefrontal 5-HT1A receptors with implications for neuropsychiatric diseases associated with emotional dysfunction, such as anxiety and depressive disorders.

KEYWORDS:

5-HT transporter; 5-HT1a receptor; Kir3.1; prefrontal cortex; serotonin; tyrosine phosphorylation

PMID:
24760870
PMCID:
PMC3996227
DOI:
10.1523/JNEUROSCI.3762-13.2014
[Indexed for MEDLINE]
Free PMC Article
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