Dissecting Neuronal Activation on a Brain-Wide Scale With Immediate Early Genes

被引:29
作者
Franceschini, Alessandra [1 ]
Costantini, Irene [1 ,2 ]
Pavone, Francesco S. [1 ,2 ,3 ]
Silvestri, Ludovico [1 ,2 ,3 ]
机构
[1] European Lab Nonlinear Spect LENS, Sesto Fiorentino, Italy
[2] Natl Res Council INO CNR, Natl Inst Opt, Sesto Fiorentino, Italy
[3] Univ Florence, Dept Phys & Astron, Florence, Italy
基金
欧盟地平线“2020”;
关键词
immediate early genes; tissue clearing; light-sheet microscopy; high-throughput microscopy; image analysis; whole-brain mapping; LIGHT-SHEET MICROSCOPY; SINGLE-CELL RESOLUTION; CENTRAL-NERVOUS-SYSTEM; IN-VIVO; C-FOS; FLUORESCENCE MICROSCOPY; BIOLOGICAL TISSUES; EXPRESSION; MEMORY; CALCIUM;
D O I
10.3389/fnins.2020.569517
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Visualizing neuronal activation on a brain-wide scale yet with cellular resolution is a fundamental technical challenge for neuroscience. This would enable analyzing how different neuronal circuits are disrupted in pathology and how they could be rescued by pharmacological treatments. Although this goal would have appeared visionary a decade ago, recent technological advances make it eventually feasible. Here, we review the latest developments in the fields of genetics, sample preparation, imaging, and image analysis that could be combined to afford whole-brain cell-resolution activation mapping. We show how the different biochemical and optical methods have been coupled to study neuronal circuits at different spatial and temporal scales, and with cell-type specificity. The inventory of techniques presented here could be useful to find the tools best suited for a specific experiment. We envision that in the next years, mapping of neuronal activation could become routine in many laboratories, allowing dissecting the neuronal counterpart of behavior.
引用
收藏
页数:17
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