Wang Depeng, Roy Suva, Rudzite Andra M, Field Greg D, Gong Yiyang
Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Department of Neurobiology, Duke University, Durham, NC 27708, USA.
Biomed Opt Express. 2021 Jun 8;12(7):3887-3901. doi: 10.1364/BOE.425742. eCollection 2021 Jul 1.
Light-field fluorescence microscopy can record large-scale population activity of neurons expressing genetically-encoded fluorescent indicators within volumes of tissue. Conventional light-field microscopy (LFM) suffers from poor lateral resolution when using wide-field illumination. Here, we demonstrate a structured-illumination light-field microscopy (SI-LFM) modality that enhances spatial resolution over the imaging volume. This modality increases resolution by illuminating sample volume with grating patterns that are invariant over the axial direction. The size of the SI-LFM point-spread-function (PSF) was approximately half the size of the conventional LFM PSF when imaging fluorescent beads. SI-LFM also resolved fine spatial features in lens tissue samples and fixed mouse retina samples. Finally, SI-LFM reported neural activity with approximately three times the signal-to-noise ratio of conventional LFM when imaging live zebrafish expressing a genetically encoded calcium sensor.
光场荧光显微镜可以记录组织体积内表达基因编码荧光指示剂的神经元的大规模群体活动。传统的光场显微镜(LFM)在使用宽场照明时横向分辨率较差。在这里,我们展示了一种结构化照明显微镜(SI-LFM)模式,它在成像体积上提高了空间分辨率。这种模式通过用在轴向不变的光栅图案照射样品体积来提高分辨率。在对荧光珠成像时,SI-LFM点扩散函数(PSF)的大小约为传统LFM PSF大小的一半。SI-LFM还解析了晶状体组织样本和固定小鼠视网膜样本中的精细空间特征。最后,在对表达基因编码钙传感器的活斑马鱼成像时,SI-LFM报告的神经活动信噪比约为传统LFM的三倍。