BRAINCITY, Nencki Institute of Experimental Biology PAS, Pasteura 3, 02-093 Warszawa, Poland.
Nencki Institute of Experimental Biology PAS, Pasteura 3, 02-093 Warszawa, Poland.
ACS Appl Mater Interfaces. 2023 Mar 15;15(10):12831-12841. doi: 10.1021/acsami.2c22985. Epub 2023 Mar 7.
Here, we provide experimental verification supporting the use of short-section imaging bundles for two-photon microscopy imaging of the mouse brain. The 8 mm long bundle is made of a pair of heavy-metal oxide glasses with a refractive index contrast of 0.38 to ensure a high numerical aperture NA = 1.15. The bundle is composed of 825 multimode cores, ordered in a hexagonal lattice with a pixel size of 14 μm and a total diameter of 914 μm. We demonstrate successful imaging through custom-made bundles with 14 μm resolution. As the input, we used a 910 nm Ti-sapphire laser with 140 fs pulse and a peak power of 9 × 10 W. The excitation beam and fluorescent image were transferred through the fiber imaging bundle. As test samples, we used 1 μm green fluorescent latex beads, ex vivo hippocampal neurons expressing green fluorescent protein and cortical neurons in vivo expressing the fluorescent reporter GCaMP6s or immediate early gene Fos fluorescent reporter. This system can be used for minimal-invasive in vivo imaging of the cerebral cortex, hippocampus, or deep brain areas as a part of a tabletop system or an implantable setup. It is a low-cost solution, easy to integrate and operate for high-throughput experiments.
在这里,我们提供了实验验证,支持使用短节成像束进行小鼠大脑的双光子显微镜成像。8 毫米长的光纤束由一对具有 0.38 折射率对比度的重金属氧化物玻璃制成,以确保高数值孔径 NA=1.15。光纤束由 825 根多模光纤组成,按照六边形晶格排列,像素大小为 14μm,总直径为 914μm。我们通过定制的分辨率为 14μm 的光纤束成功地进行了成像。作为输入,我们使用了 910nm 的钛宝石激光器,其脉冲宽度为 140fs,峰值功率为 9×10W。激发光束和荧光图像通过光纤成像束传输。作为测试样本,我们使用了 1μm 绿色荧光乳胶珠、体外表达绿色荧光蛋白的海马神经元和体内表达荧光报告基因 GCaMP6s 或即刻早期基因 Fos 荧光报告基因的皮质神经元。该系统可用于大脑皮层、海马体或深部脑区的微创体内成像,作为台式系统或可植入装置的一部分。它是一种低成本的解决方案,易于集成和操作,适用于高通量实验。