Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Sci Rep. 2022 Jun 17;12(1):10205. doi: 10.1038/s41598-022-14166-1.
Understanding peripheral nerve micro-anatomy can assist in the development of safe and effective neuromodulation devices. However, current approaches for imaging nerve morphology at the fiber level are either cumbersome, require substantial instrumentation, have a limited volume of view, or are limited in resolution/contrast. We present alternative methods based on MUSE (Microscopy with Ultraviolet Surface Excitation) imaging to investigate peripheral nerve morphology, both in 2D and 3D. For 2D imaging, fixed samples are imaged on a conventional MUSE system either label free (via auto-fluorescence) or after staining with fluorescent dyes. This method provides a simple and rapid technique to visualize myelinated nerve fibers at specific locations along the length of the nerve and perform measurements of fiber morphology (e.g., axon diameter and g-ratio). For 3D imaging, a whole-mount staining and MUSE block-face imaging method is developed that can be used to characterize peripheral nerve micro-anatomy and improve the accuracy of computational models in neuromodulation. Images of rat sciatic and human cadaver tibial nerves are presented, illustrating the applicability of the method in different preclinical models.
了解周围神经的微观解剖结构有助于开发安全有效的神经调节设备。然而,目前用于在纤维水平上成像神经形态的方法要么繁琐,要么需要大量仪器,要么视场有限,要么分辨率/对比度有限。我们提出了基于 MUSE(紫外表面激发显微镜)成像的替代方法来研究周围神经形态,包括 2D 和 3D。对于 2D 成像,固定样本在常规的 MUSE 系统上进行成像,既可以无标记(通过自体荧光),也可以在荧光染料染色后进行成像。这种方法提供了一种简单快速的技术,可以在神经的特定位置可视化有髓神经纤维,并进行纤维形态(例如,轴突直径和 g-ratio)的测量。对于 3D 成像,开发了一种全切片染色和 MUSE 块面成像方法,可用于描述周围神经的微观解剖结构,并提高神经调节计算模型的准确性。展示了大鼠坐骨神经和人体尸检胫骨神经的图像,说明了该方法在不同的临床前模型中的适用性。