Photoacoustic detection of genetically encoded fluorophores for neuronal subtype identification.

Joel Lusk, Ethan Marschall, Christopher Miranda, Christina Aridi, Barbara Smith
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Abstract

Objective.Elucidating neurological processes in the mammalian brain requires improved methods for imaging and detecting neuronal subtypes. Transgenic mouse models utilizing Cre/lox recombination have been developed to selectively label neuronal subtypes with fluorophores, however, light-scattering attenuation of both excitation light and emission light limits their effective range of detection.Approach. To overcome these limitations, this study investigates the use of a near-infrared fluorophore, iRFP713, for subtype labeling of neurons found within brain regions that are typically inaccessible by optical methods. Towards this goal, a custom photoacoustic (PA) system is developed for detection of iRFP in neurons in brain slices, expressed via Cre/lox, and withinin vitrocell culture.Main results. In this study, a custom system is developed to detect iRFP in neuronal cells both in brain slices andin vitro. Furthermore, this work validates iRFP expression in the brains of transgenic mice and neuronal cell culture.Significance. Combining iRFP with advanced imaging and detection strategies, such as PA microscopy, is critical for expanding the type and variety of neurons that scientists can observe within the mammalian brain.

用于神经元亚型鉴定的遗传编码荧光团的光声检测。
目的:阐明哺乳动物大脑的神经过程需要改进成像和检测神经元亚型的方法。利用Cre/lox重组的转基因小鼠模型已经被开发出来,可以用荧光团选择性地标记神经元亚型,然而,激发光和发射光的光散射衰减限制了它们的有效检测范围。方法:为了克服这些限制,本研究调查了近红外荧光团iRFP713的使用,用于在通常通过光学方法无法进入的大脑区域内发现的神经元的亚型标记。为了实现这一目标,开发了一种定制的光声系统,用于检测脑切片中神经元中的iRFP,通过Cre/lox表达,并在体外细胞培养中表达。结果:在本研究中,开发了一种定制系统来检测脑切片和体外神经元细胞中的iRFP。此外,本工作验证了iRFP在转基因小鼠大脑和神经元细胞培养中的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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