A subset of nNOS+ interneurons derive from the CGE and coexpresses VIP

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A subset of nNOS+ interneurons derive from the CGE and coexpresses VIP A subset of nNOS+ interneurons derive from the CGE and coexpresses VIP. A, Image illustrating the coexpression of VIP and nNOS in wild-type mouse. A subset of nNOS+ interneurons derive from the CGE and coexpresses VIP. A, Image illustrating the coexpression of VIP and nNOS in wild-type mouse. Scale bar: 25 μm. B, In green, the number of cells coexpressing nNOS and VIP presented as a percentage of the total number of VIP+ cells (n = 240). In red, contribution of VIP-expressing interneurons to the population of nNOS+ cells in CA1 (n = 631) C, Neurolucida reconstruction of a VIP+/nNOS+ interneuron following electrophysiological recording. D, Voltage responses of cell shown in C to three current step injections (−80 pA, just suprathreshold, and twice suprathreshold stimulation). E, Phase plot of the voltage response shown in D to 2× suprathreshold current injection. Inset illustrates overlaid action potentials; scale bar: 10 mV, 2 ms. F, Single-cell RT-PCR analysis of the cell shown in C. Numbers under the gel give the RT-PCR summary data for all VIP+/nNOS+ interneurons recorded. G, Example of nNOS expression in fate-mapped interneurons in mature hippocampus of Mash1BAC-CreER/RCE:LoxP mouse after tamoxifen administration at E16.5. Scale bar: 25 μm. H, Contribution of nNOS+ interneurons to the cohort arising from CGE between E12.5 and E16.5. Ludovic Tricoire et al. J. Neurosci. 2010;30:2165-2176 ©2010 by Society for Neuroscience