Expression of neuronal nicotinic acetylcholine receptor subunit mRNAs in rat hippocampal GABAergic interneurons

摘要

Hippocampal inhibitory interneurons are a diverse population of cells widely scattered in hippocampus, where they regulate hippocampal circuit activity. The hippocampus receives cholinergic projections from the basal forebrain, and functional studies have suggested the presence of different subtypes of nicotinic acetylcholine receptors (AChR) on GABAergic interneurons. Single cell PCR-analysis had confirmed that several nAChR subunit mRNAs are coexpressed with glutamate decarboxylase 67 (GAD67), the marker for GABAergic interneurons. In this anatomical study, we systematically investigated the coexpression of GAD67 with different nAChR subunits using double in situ hybridization with a digoxigenin-labeled GAD67 probe and ³⁵S-labeled probes for nAChR subunits (α2, α3, α4, α5, α6, α7, β2, β3, and β4). The results revealed that most GAD67-positive interneurons expressed β2, and 67 % also expressed α7 mRNA. In contrast, mRNA expression of other subunits was limited; only 13 % of GAD67-positive neurons coexpressed α4, and less than 10% expressed transcripts for α2, α3, α5 or β4. Most GAD67/α2 coexpression was located in CA1/CA3 stratum oriens, and GAD67/α5 coexpression was predominantly detected in CA1/CA3 stratum radiatum/lacunosum moleculare and the dentate gyrus. Expression of α6 and β3 mRNAs was rarely detected in the hippocampus, and mRNAs were not coexpressed with GAD67. These findings suggest that the majority of nicotinic responses in GABAergic interneurons should be mediated by a homomeric α7 or heteromeric α7*-containing nAChRs. Other possible combinations such as α2β2*, α4β2*, or α5β2* heteromeric nAChRs could contribute to functional nicotinic response in subsets of GABAergic interneurons but overall would have a minor role.