Striatal Neurons Expressing D1 and D2 Receptors are Morphologically Distinct and Differently Affected by Dopamine Denervation in Mice
Identifieur interne : 000023 ( Main/Exploration ); précédent : 000022; suivant : 000024Striatal Neurons Expressing D1 and D2 Receptors are Morphologically Distinct and Differently Affected by Dopamine Denervation in Mice
Auteurs : D. Gagnon [Canada] ; S. Petryszyn [Canada] ; M. G. Sanchez [Canada] ; C. Bories [Canada] ; J. M. Beaulieu [Canada] ; Y. De Koninck [Canada] ; A. Parent [Canada] ; M. Parent [Canada]Source :
- Scientific Reports [ 2045-2322 ] ; 2017.
Abstract
The loss of nigrostriatal dopamine neurons in Parkinson’s disease induces a reduction in the number of dendritic spines on medium spiny neurons (MSNs) of the striatum expressing D1 or D2 dopamine receptor. Consequences on MSNs expressing both receptors (D1/D2 MSNs) are currently unknown. We looked for changes induced by dopamine denervation in the density, regional distribution and morphological features of D1/D2 MSNs, by comparing 6-OHDA-lesioned double BAC transgenic mice (
Url:
DOI: 10.1038/srep41432
PubMed: 28128287
PubMed Central: 5269744
Affiliations:
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Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Striatal Neurons Expressing D<sub>1</sub>
and D<sub>2</sub>
Receptors are Morphologically Distinct and Differently Affected by Dopamine Denervation in Mice</title>
<author><name sortKey="Gagnon, D" sort="Gagnon, D" uniqKey="Gagnon D" first="D." last="Gagnon">D. Gagnon</name>
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</nlm:aff>
<country xml:lang="fr">Canada</country>
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<series><title level="j">Scientific Reports</title>
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<front><div type="abstract" xml:lang="en"><p>The loss of nigrostriatal dopamine neurons in Parkinson’s disease induces a reduction in the number of dendritic spines on medium spiny neurons (MSNs) of the striatum expressing D<sub>1</sub>
or D<sub>2</sub>
dopamine receptor. Consequences on MSNs expressing both receptors (D<sub>1</sub>
/D<sub>2</sub>
MSNs) are currently unknown. We looked for changes induced by dopamine denervation in the density, regional distribution and morphological features of D<sub>1</sub>
/D<sub>2</sub>
MSNs, by comparing 6-OHDA-lesioned double BAC transgenic mice (<italic>Drd1a</italic>
-tdTomato/<italic>Drd2</italic>
-EGFP) to sham-lesioned animals. D<sub>1</sub>
/D<sub>2</sub>
MSNs are uniformly distributed throughout the dorsal striatum (1.9% of MSNs). In contrast, they are heterogeneously distributed and more numerous in the ventral striatum (14.6% in the shell and 7.3% in the core). Compared to D<sub>1</sub>
and D<sub>2</sub>
MSNs, D<sub>1</sub>
/D<sub>2</sub>
MSNs are endowed with a smaller cell body and a less profusely arborized dendritic tree with less dendritic spines. The dendritic spine density of D<sub>1</sub>
/D<sub>2</sub>
MSNs, but also of D<sub>1</sub>
and D<sub>2</sub>
MSNs, is significantly reduced in 6-OHDA-lesioned mice. In contrast to D<sub>1</sub>
and D<sub>2</sub>
MSNs, the extent of dendritic arborization of D<sub>1</sub>
/D<sub>2</sub>
MSNs appears unaltered in 6-OHDA-lesioned mice. Our data indicate that D<sub>1</sub>
/D<sub>2</sub>
MSNs in the mouse striatum form a distinct neuronal population that is affected differently by dopamine deafferentation that characterizes Parkinson’s disease.</p>
</div>
</front>
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