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Cereb Cortex ; 33(8): 4293-4304, 2023 04 04.
Artigo em Inglês | MEDLINE | ID: mdl-36030380

RESUMO

Neocortical vasoactive intestinal polypeptide-expressing (VIP+) interneurons display highly diverse morpho-electrophysiological and molecular properties. To begin to understand the function of VIP+ interneurons in cortical circuits, they must be clearly and comprehensively classified into distinct subpopulations based on specific molecular markers. Here, we utilized patch-clamp RT-PCR (Patch-PCR) to simultaneously obtain the morpho-electric properties and mRNA profiles of 155 VIP+ interneurons in layers 2 and 3 (L2/3) of the mouse somatosensory cortex. Using an unsupervised clustering method, we identified 3 electrophysiological types (E-types) and 2 morphological types (M-types) of VIP+ interneurons. Joint clustering based on the combined electrophysiological and morphological features resulted in 3 morpho-electric types (ME-types). More importantly, we found these 3 ME-types expressed distinct marker genes: ~94% of Sncg+ cells were ME-type 1, 100% of Mybpc1+ cells were ME-type 2, and ~78% of Parm1+ were ME-type 3. By clarifying the properties of subpopulations of cortical L2/3 VIP+ interneurons, this study establishes a basis for future investigations aiming to elucidate their physiological roles.


Assuntos
Córtex Somatossensorial , Peptídeo Intestinal Vasoativo , Animais , Camundongos , Fenômenos Eletrofisiológicos , Interneurônios/fisiologia , Córtex Somatossensorial/fisiologia , Peptídeo Intestinal Vasoativo/metabolismo , Proteínas de Neoplasias/metabolismo , gama-Sinucleína/metabolismo , Proteína de Ligação a Androgênios/metabolismo
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