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通过椭圆形随机采集神经成像实现的快速双光子显微镜技术(NORA)。

Fast Two-photon Microscopy by Neuroimaging with Oblong Random Acquisition (NORA).

作者信息

Whang Esther M, Thomas Skyler, Yi Ji, Charles Adam S

机构信息

Department of Biomedical Engineering, Center for Imaging Science, Johns Hopkins University, Baltimore, MD 21218.

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218.

出版信息

ArXiv. 2025 Mar 19:arXiv:2503.15487v1.

Abstract

Advances in neural imaging have enabled neuroscience to study how the joint activity of large neural populations conspire to produce perception, behavior and cognition. Despite many advances in optical methods, there exists a fundamental tradeoff between imaging speed, field of view, and resolution that limits the scope of neural imaging, especially for the raster-scanning multi-photon imaging needed for imaging deeper into the brain. One approach to overcoming this trade-off is in computational imaging: the co-development of optics and algorithms where the optics are designed to encode the target images into fewer measurements that are faster to acquire, and the algorithms compensate by inverting the optical image coding process to recover a larger or higher resolution image. We present here one such approach for raster-scanning two-photon imaging: Neuroimaging with Oblong Random Acquisition (NORA). NORA quickly acquires each frame in a microscopic video by subsampling only a fraction of the fast scanning lines, ignoring large portions of each frame. NORA mitigates the loss of information by extending the point-spread function in the slow-scan direction to effectively integrate the fluorescence of neighboring lines together into a single set of measurements. By imaging different, randomly selected, lines at each frame, NORA diversifies the information content across frames and enabling a video-level reconstruction. Rather than reconstruct the video frame-by-frame using an image-level recovery algorithm, NORA recovers full video sequences through a nuclear-norm minimization (i.e., matrix completion) on the pixels-by-time matrix. We simulated NORA imaging using the Neural Anatomy and Optical Microscopy (NAOMi) biophysical simulation suite. Using these simulations we demonstrate that NORA imaging can accurately recover 400 m X 400 m fields of view at subsampling rates up to 20X, despite realistic noise and motion conditions. As NORA requires minimal changes to current microscopy systems, our results indicate that NORA can provide a promising avenue towards fast imaging of neural circuits.

摘要

神经成像技术的进步使神经科学能够研究大量神经群体的联合活动如何共同产生感知、行为和认知。尽管光学方法取得了许多进展,但在成像速度、视野和分辨率之间存在着基本的权衡,这限制了神经成像的范围,特别是对于深入大脑成像所需的光栅扫描多光子成像。克服这种权衡的一种方法是计算成像:光学和算法的共同开发,其中光学系统被设计用于将目标图像编码为更少的测量值,以便更快地获取,而算法则通过反转光学图像编码过程来进行补偿,以恢复更大或更高分辨率的图像。我们在此介绍一种用于光栅扫描双光子成像的方法:椭圆形随机采集神经成像(NORA)。NORA通过仅对一小部分快速扫描线进行子采样来快速获取微观视频中的每一帧,忽略每一帧的大部分内容。NORA通过在慢扫描方向上扩展点扩散函数来减轻信息损失,从而有效地将相邻线的荧光整合到一组测量值中。通过在每一帧对不同的、随机选择的线进行成像,NORA使各帧之间的信息内容多样化,并实现视频级重建。NORA不是使用图像级恢复算法逐帧重建视频,而是通过对像素-时间矩阵进行核范数最小化(即矩阵补全)来恢复完整的视频序列。我们使用神经解剖学和光学显微镜(NAOMi)生物物理模拟套件对NORA成像进行了模拟。通过这些模拟,我们证明,尽管存在现实的噪声和运动条件,NORA成像仍能以高达20倍的子采样率准确恢复400μm×400μm的视野。由于NORA对当前显微镜系统的改动最小,我们的结果表明,NORA可为神经回路的快速成像提供一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/756e/12281901/0a32d2f896d1/nihpp-2503.15487v2-f0001.jpg

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