Characterization of type I and type II nNOS-expressing interneurons in the barrel cortex of mouse

被引:66
作者
Perrenoud, Quentin [1 ]
Geoffroy, Helene [1 ]
Gauthier, Benjamin [1 ]
Rancillac, Armelle [1 ]
Alfonsi, Fabienne [2 ,3 ]
Kessaris, Nicoletta [2 ,3 ]
Rossier, Jean [1 ]
Vitalis, Tania [1 ]
Gallopin, Thierry [1 ]
机构
[1] Univ Paris 06, CNRS, Neurobiol Lab, ESPCI ParisTech,UMR 7637, F-75005 Paris, France
[2] UCL, Wolfson Inst Biomed Res, London, England
[3] UCL, Dept Cell & Dev Biol, London, England
来源
FRONTIERS IN NEURAL CIRCUITS | 2012年 / 6卷
基金
欧洲研究理事会;
关键词
Immunohistochemistry; patch-clamp; development; nitric oxide; parvalbumin; somatostatin; vasointestinal peptide; neuropeptide Y; NITRIC-OXIDE SYNTHASE; NADPH-DIAPHORASE HISTOCHEMISTRY; CALCIUM-BINDING PROTEINS; MONKEY CEREBRAL-CORTEX; LOCAL-CIRCUIT NEURONS; RAT VISUAL-CORTEX; CORTICAL INTERNEURONS; GABAERGIC NEURONS; NEOCORTICAL INTERNEURONS; NONPYRAMIDAL CELLS;
D O I
10.3389/fncir.2012.00036
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the neocortex, neuronal nitric oxide (NO) synthase (nNOS) is essentially expressed in two classes of GABAergic neurons: type I neurons displaying high levels of expression and type II neurons displaying weaker expression. Using immunocytochemistry in mice expressing GFP under the control of the glutamic acid decarboxylase 67 k (promoter, we studied the distribution of type I and type II neurons in the barrel cortex and their expression of parvalbumin (PV), somatostatin (SOM), and vasoactive intestinal peptide (VIP). We found that type I neurons were predominantly located in deeper layers and expressed SOM (91.5%) while type II neurons were concentrated in layer II/III and VI and expressed PV ( 17.7%), SOM (18.7%), and VIP (10.2%). We then characterized neurons expressing nNOS mRNA (n = 42 cells) ex vivo, using whole-cell recordings coupled to single cell reverse transcription-PCR and biocytin labeling. Unsupervised cluster analysis of this sampled is closed four classes. One cluster (n = 7) corresponded to large, deep layer neurons, displaying a high expression of SOM (85.7%) and was thus very likely to correspond to type I neurons. The three other clusters were identified as putative type II cells and corresponded to neurogliaform-like interneurons (n = 19), deep layer neurons expressing PV or SOM (n = 9), and neurons expressing VIP (n = 7). Finally, we performed nNOS immunohistochemistry on mouse lines in which GFP labeling revealed the expression of two specific developmental genes (Lhx6 and 5-HT3A). We found that type I neurons expressed Lhx6 but never 5HT(3A), indicating that they originate in the medial ganglionic eminence (MGE). Type II neurons expressed Lhx6 (63%) and 5-HT3A (34.4%) supporting their derivation either from the MGE or from the caudal ganglionic eminence (CGE) and the entopeduncular and dorsal preoptic areas. Together, our results in the barrel cortex of mouse support the view that type I neurons form a specific class of SOM-expressing neurons while type II neurons comprise atleast three classes.
引用
收藏
页码:1 / 31
页数:17
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