Janelia Farm Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, Virginia 20147, USA.
Nature. 2013 Jul 18;499(7458):295-300. doi: 10.1038/nature12354.
Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice in vivo. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5-40-µm long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
荧光钙传感器被广泛用于神经活动的成像。通过基于结构的诱变和基于神经元的筛选,我们开发了一系列超灵敏的蛋白钙传感器(GCaMP6),在培养的神经元以及斑马鱼、果蝇和小鼠体内,其性能优于其他传感器。在小鼠视觉皮层的 2/3 层锥体神经元中,GCaMP6 可靠地检测到神经元胞体中的单个动作电位以及单个树突棘中的定向调节突触钙瞬变。结构持续存在的树突棘的定向调节在数周的时间尺度上基本稳定。跨越整个树突棘群体的平均定向调节预测了其母细胞的调节。虽然 GABA 能神经元的胞体显示出很少的定向调节,但它们的树突包括高度调节的树突段(5-40-µm 长)。因此,GCaMP6 传感器为在多个空间和时间尺度上研究神经回路的组织和动态提供了新的窗口。