Department of Molecular and Cellular Biology, Center for Brain Science, Harvard University, Cambridge, Massachusetts, USA.
Nat Neurosci. 2010 Apr;13(4):513-20. doi: 10.1038/nn.2518. Epub 2010 Mar 21.
Existing techniques for monitoring neural activity in awake, freely behaving vertebrates are invasive and difficult to target to genetically identified neurons. We used bioluminescence to non-invasively monitor the activity of genetically specified neurons in freely behaving zebrafish. Transgenic fish with the Ca(2+)-sensitive photoprotein green fluorescent protein (GFP)-Aequorin in most neurons generated large and fast bioluminescent signals that were related to neural activity, neuroluminescence, which could be recorded continuously for many days. To test the limits of this technique, we specifically targeted GFP-Aequorin to the hypocretin-positive neurons of the hypothalamus. We found that neuroluminescence generated by this group of approximately 20 neurons was associated with periods of increased locomotor activity and identified two classes of neural activity corresponding to distinct swim latencies. Our neuroluminescence assay can report, with high temporal resolution and sensitivity, the activity of small subsets of neurons during unrestrained behavior.
现有的在清醒、自由活动的脊椎动物中监测神经活动的技术具有侵入性,并且难以针对基因鉴定的神经元进行靶向操作。我们使用生物发光技术非侵入性地监测自由活动的斑马鱼中基因特异性神经元的活动。在大多数神经元中具有钙敏感性光蛋白绿色荧光蛋白(GFP)-Aequorin 的转基因鱼产生了与神经活动相关的大而快速的生物发光信号,该信号可以连续记录多天。为了测试该技术的极限,我们将 GFP-Aequorin 专门靶向下丘脑的食欲素阳性神经元。我们发现,这组大约 20 个神经元产生的神经发光与运动活动增加的时期有关,并确定了两种与不同游泳潜伏期相对应的神经活动类型。我们的神经发光测定法可以以高时间分辨率和灵敏度报告不受限制的行为过程中小部分神经元的活动。