IL-10 Gene Knockout Reduces the Expression of mGlu Receptor 1a/b and Decreases the Glutamate-Dependent Production of Nitric Oxide
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Author(s)
IL-10 provides trophic and survival effects directly
on neurons, promotes axonal outgrowth, and stimulates
neuroregeneration. In this study, we analyzed the activities of arginase
and nitric oxide synthase (NOS) in synaptoneurosomes derived from brain
cortex of C57BL/6 IL-10 gene-knockout (KO) and wild-type (Wt) mice and
determined that the synaptoneurosomes derived from KO mice present lower
arginase II activity and lower spermine content than those derived from
Wt mice, whereas the basal NOS activity in the KO synaptoneurosomes was
higher than that observed in the control synaptoneurosomes. Moreover,
our results indicate that the plasma membranes isolated from the KO mice
brain exhibit significantly lower spermine-induced enhancement of [3H]
MK-801 binding than the plasma membranes from the brain of Wt mice.
Glutamate increases the production of nitric oxide (NO) in Wt
synaptoneurosomes in a dose-dependent manner, whereas in the KO
synaptoneurosomes, this amino acid does not affect the synthesis of NO.
The glutamate-dependent acceleration of NO synthesis in Wt
synaptoneurosomes was abrogated by LY367385, an antagonist of mGluR1a/b.
The western blot analysis of the synaptoneurosomal proteins
demonstrates that the expression of the subunits of NMDAR (NMDAR2A and
NMDAR2B), the level of NMDAR-bound nNOS and the expression of iNOS are
not changed in KO mice and that only the level of mGluR1a/b is markedly
reduced in the synaptoneurosomes of KO mice. We conclude that a
neuroprotective and neuroregenerative property of IL-10, in addition to
its effects on polyamine metabolism and the spermine-dependent
modulation of NMDAR, may involve the regulation of mGluR1a/b expression.
Cite this paper
Koriauli, S. , Barbakadze, T. , Natsvlishvili, N. ,
Dabrundashvili, N. , Kvaratskhelia, E. and Mikeladze, D. (2014) IL-10
Gene Knockout Reduces the Expression of mGlu Receptor 1a/b and
Decreases the Glutamate-Dependent Production of Nitric Oxide. Journal of Biomedical Science and Engineering, 7, 1019-1029. doi: 10.4236/jbise.2014.713099.
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