Strain‐specific proportion of the two isoforms of the dopamine D2 receptor in the mouse striatum: associated neural and behavioral phenotypes

• Published in: Genes, brain and behavior brain and behavior, 2010-10, Vol.9 (7), p.703-711
• Main Authors: Colelli, V., Fiorenza, M. T., Conversi, D., Orsini, C., Cabib, S.
• Format: Article
• Language: English
• Subjects: Accumbens core; addiction; alternative splicing; Animals; Behavior, Animal - physiology; Corpus Striatum - metabolism; dopamine; dorsomedial striatum; fos; Genes, fos - genetics; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Neural Pathways - metabolism; Nucleus Accumbens - metabolism; Receptors, Dopamine D1 - genetics; Receptors, Dopamine D1 - metabolism; Receptors, Dopamine D2 - genetics; Receptors, Dopamine D2 - metabolism; Receptors, Dopamine D3 - genetics; Receptors, Dopamine D3 - metabolism; Reverse Transcriptase Polymerase Chain Reaction; RNA - biosynthesis; RNA - genetics; schizophrenia; Species Specificity; Stereotyped Behavior - physiology; stereotypy; striosomes
• ISSN: 1601-1848; 1601-183X
• DOI: 10.1111/j.1601-183X.2010.00604.x

Genetic variability in the proportion of the two alternative dopamine D2 receptor (D2R) mRNA splice variants, D2R‐long (D2L) and D2R‐short (D2S), influence corticostriatal functioning and could be implicated in liability to psychopathology. This study compared mesostriatal D2L/D2S ratios and associated neural and behavioral phenotypes in mice of the DBA/2J and C57BL/6J‐inbred strains, which differ for schizophrenia‐ and addiction‐like phenotypes. Results showed that DBA/2J mice lack the striatal predominance of D2L that has been reported in the rat and in C57BL/6J mice and confirmed in the latter strain by this study. Only C57BL/6J mice showed enhanced striatal c‐Fos expression under D1R and D2/3R co‐stimulation, indicating synergistic interaction between the subtypes of DA receptors. Instead, DBA/2J mice were characterized by opposing effects of D2/3R and D1R stimulation on striatal c‐Fos expression, in line with a more pronounced influence of D2S isoform, and did not express stereotyped climbing under D1R and D2/3R co‐stimulation, as reported for D2L−/− mice. Finally, strain‐specific modulation of c‐Fos expression by D1R and D2/3R co‐stimulation was selectively observed in striatal compartments receiving inputs from the prefrontal cortex and involved in the control of motivated behaviors. These results show differences in tissue‐specific D2R splicing in mice with intact genotypes and support a role for this phenotype in individual variability of corticostriatal functioning and in liability to psychopathology.