Dcc haploinsufficiency regulates dopamine receptor expression across postnatal lifespan.

TitleDcc haploinsufficiency regulates dopamine receptor expression across postnatal lifespan.
Publication TypeJournal Article
Year of Publication2017
AuthorsPokinko M, Grant A, Shahabi F, Dumont Y, Manitt C, Flores C
JournalNeuroscience
Volume346
Pagination182-189
Date Published2017 Mar 27
ISSN1873-7544
Abstract

Adolescence is a period during which the medial prefrontal cortex (mPFC) undergoes significant remodeling. The netrin-1 receptor, deleted in colorectal cancer (DCC), controls the extent and organization of mPFC dopamine connectivity during adolescence and in turn directs mPFC functional and structural maturation. Dcc haploinsufficiency leads to increased mPFC dopamine input, which causes improved cognitive processing and resilience to behavioral effects of stimulant drugs of abuse. Here we examine the effects of Dcc haploinsufficiency on the dynamic expression of dopamine receptors in forebrain targets of C57BL6 mice. We conducted quantitative receptor autoradiography experiments with [(3)H]SCH-23390 or [(3)H]raclopride to characterize D1 and D2 receptor expression in mPFC and striatal regions in male Dcc haploinsufficient and wild-type mice. We generated autoradiograms at early adolescence (PND21±1), mid-adolescence (PND35±2), and adulthood (PND75±15). C57BL6 mice exhibit overexpression and pruning of D1, but not D2, receptors in striatal regions, and a lack of dopamine receptor pruning in the mPFC. We observed age- and region-specific differences in D1 and D2 receptor density between Dcc haploinsufficient and wild-type mice. Notably, neither group shows the typical pattern of mPFC dopamine receptor pruning in adolescence, but adult haploinsufficient mice show increased D2 receptor density in the mPFC. These results show that DCC receptors contribute to the dynamic refinement of D1 and D2 receptor expression in striatal regions across adolescence. The age-dependent expression of dopamine receptor in C57BL6 mice shows marked differences from previous characterizations in rats.

DOI10.1016/j.neuroscience.2017.01.009
Alternate JournalNeuroscience
PubMed ID28108253
PubMed Central IDPMC5337141
Grant ListR01 DA037911 / DA / NIDA NIH HHS / United States