Ohayon Shay, Caravaca-Aguirre Antonio, Piestun Rafael, DiCarlo James J
McGovern Institute for Brain Research, Massachusetts Institute of Technology, 43 Vassar Street, Cambridge, MA 02139, USA.
Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, 77 Massachusetts Ave, Cambridge, MA 02139, USA.
Biomed Opt Express. 2018 Mar 6;9(4):1492-1509. doi: 10.1364/BOE.9.001492. eCollection 2018 Apr 1.
A major open challenge in neuroscience is the ability to measure and perturb neural activity in vivo from well defined neural sub-populations at cellular resolution anywhere in the brain. However, limitations posed by scattering and absorption prohibit non-invasive multi-photon approaches for deep (>2mm) structures, while gradient refractive index (GRIN) endoscopes are relatively thick and can cause significant damage upon insertion. Here, we present a novel micro-endoscope design to image neural activity at arbitrary depths via an ultra-thin multi-mode optical fiber (MMF) probe that has 5-10X thinner diameter than commercially available micro-endoscopes. We demonstrate micron-scale resolution, multi-spectral and volumetric imaging. In contrast to previous approaches, we show that this method has an improved acquisition speed that is sufficient to capture rapid neuronal dynamics in-vivo in rodents expressing a genetically encoded calcium indicator (GCaMP). Our results emphasize the potential of this technology in neuroscience applications and open up possibilities for cellular resolution imaging in previously unreachable brain regions.
神经科学领域一个重大的开放性挑战是,能否在细胞分辨率下,从大脑中任何位置明确界定的神经亚群体内测量并扰动神经活动。然而,散射和吸收带来的限制使得非侵入性多光子方法无法用于深部(>2mm)结构,而梯度折射率(GRIN)内窥镜相对较粗,插入时可能造成显著损伤。在此,我们提出一种新型微内窥镜设计,通过一根直径比市售微内窥镜细5至10倍的超薄多模光纤(MMF)探头,对任意深度的神经活动进行成像。我们展示了微米级分辨率、多光谱和体积成像。与先前方法不同的是,我们表明该方法具有更高的采集速度,足以在表达基因编码钙指示剂(GCaMP)的啮齿动物体内捕捉快速的神经元动态。我们的结果强调了该技术在神经科学应用中的潜力,并为在以前无法到达的脑区进行细胞分辨率成像开辟了可能性。