Cell type-specific distribution of GABA receptor subtypes in the mouse dorsal striatum.

The striatum is the main input nucleus of the basal ganglia, mediating motor and cognitive functions. Striatal projection neurons are GABAergic medium spiny neurons (MSN), expressing either the dopamine receptor type 1 (D -R MSN) and forming the direct, movement-promoting pathway, or dopamine receptor type 2 (D -R MSN), forming the indirect movement-suppressing pathway. Locally, activity and synchronization of MSN are modulated by several subtypes of GABAergic and cholinergic interneurons. Overall, GABAergic circuits in the striatum remain poorly characterized, and little is known about the intrastriatal connectivity of interneurons and the distribution of GABA receptor (GABA R) subtypes, distinguished by their subunit composition, in striatal synapses. Here, by using immunofluorescence in mouse tissue, we investigated the distribution of GABA Rs containing the α , α , or α subunit in perisomatic synapses of striatal MSN and interneurons, as well as the innervation pattern of D R- and D R-MSN soma and axonal initial segment (AIS) by GABAergic and cholinergic interneurons. Our results show that perisomatic GABAergic synapses of D R- and D R-MSN contain the GABA R α and/or α subunits, but not the α subunit; D R-MSN have significantly more α -GABA Rs on their soma than D R-MSN. Further, interneurons have few perisomatic synapses containing α -GABA Rs, whereas α -GABA Rs (along with the α -GABA Rs) are abundant in perisomatic synapses of CCK , NPY /SOM , and vAChT interneurons. Each MSN and interneuron population analyzed received a distinct pattern of GABAergic and cholinergic innervation, complementing this postsynaptic heterogeneity. In conclusion, intra-striatal GABAergic circuits are distinguished by cell-type specific innervation patterns, differential expression and postsynaptic targeting of GABA R subtypes.