کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2041011 | 1073140 | 2012 | 12 صفحه PDF | دانلود رایگان |

SummaryCellular resolution three-dimensional (3D) visualization of defined, fluorescently labeled long-range neuronal networks in the uncut adult mouse brain has been elusive. Here, a virus-based strategy is described that allowed fluorescent labeling of centrifugally projecting neuronal populations in the ventral forebrain and their directly, monosynaptically connected bulbar interneurons upon a single stereotaxic injection into select neuronal populations. Implementation of improved tissue clearing combined with light-sheet fluorescence microscopy permitted imaging of the resulting connectivity maps in a single whole-brain scan. Subsequent 3D reconstructions revealed the exact distribution of the diverse neuronal ensembles monosynaptically connected with distinct bulbar interneuron populations. Moreover, rehydratation of brains after light-sheet fluorescence imaging enabled the immunohistochemical identification of synaptically connected neurons. Thus, this study describes a method for identifying monosynaptic connectivity maps from distinct, virally labeled neuronal populations that helps in better understanding of information flow in neural systems.
Graphical AbstractFigure optionsDownload as PowerPoint slideHighlights
► Two-color light-sheet fluorescence microscopic imaging of adult mouse brains
► Virus-mediated monosynaptic tracing from defined neurons by single virus application
► Fluorescent protein preservation of rehydrated brains after light-sheet microscopy
► Visualization of olfactory connectomes for directly projecting forebrain neurons
Journal: - Volume 2, Issue 5, 29 November 2012, Pages 1375–1386