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| Abstract |
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Interferon (IFN)–
upregulates serotonin (5–HT)
uptake and serotonin transporter (5–HTT) messenger ribonucleic acid (mRNA)
expression in immune cells, which implies the mechanism underlying
IFN–
–induced depression. However, the signal
transduction of this effect remains unclear. We investigated whether the effects of
IFN–
on the functions of 5–HTT were related to
mitogen–activated protein kinase (MAPK). By performing Western blotting,
real–time reverse transcriptase-polymerase chain reaction and
[3H]5–HT labelling, we examined MAPK phosphorylation,
5–HTT mRNA expression and 5–HT uptake in Jurkat T cells. The
cells had been cultured for different time periods (1) with
IFN–
alone and (2) preincubated with either MAPK inhibitors or
with the selective serotonin reuptake inhibitor, fluoxetine, and subsequently
cultured along with IFN–
. The levels of MAPK phosphorylation,
5–HTT mRNA expression and 5–HT uptake all increased in the
IFN–
–treated cells but were blocked in those that
were pretreated with MAPK inhibitors and fluoxetine. These results appear to clarify
the association of depression with
IFN–
–induced 5–HT uptake that
reduces the 5–HT levels and IFN–
–regulated
transcription of 5–HTT; further, the results suggest the involvement of
MAPK in this process.
Key Words: depression, interferon, mitogen–activated protein kinase, serotonin transporter
First published on February 28, 2008, doi:10.1177/0269881107082951
Journal of Psychopharmacology 2008;22:753.
A more recent version of this article appeared on September 1, 2008
This version was published on April
15, 2008
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–induced serotonin uptake in Jurkat
T cells via mitogen–activated protein kinase and transcriptional regulation of
the serotonin transporter