McKnight Brain Institute, Dep. of Neuroscience, University of Florida, FL, USA.
Neuroimage. 2012 Apr 2;60(2):1404-11. doi: 10.1016/j.neuroimage.2012.01.050. Epub 2012 Jan 14.
With its unparalleled ability to safely generate high-contrast images of soft tissues, magnetic resonance imaging (MRI) has remained at the forefront of diagnostic clinical medicine. Unfortunately due to resolution limitations, clinical scans are most useful for detecting macroscopic structural changes associated with a small number of pathologies. Moreover, due to a longstanding inability to directly observe magnetic resonance (MR) signal behavior at the cellular level, such information is poorly characterized and generally must be inferred. With the advent of the MR microscope in 1986 came the ability to measure MR signal properties of theretofore unobservable tissue structures. Recently, further improvements in hardware technology have made possible the ability to visualize mammalian cellular structure. In the current study, we expand upon previous work by imaging the neuronal cell bodies and processes of human and porcine α-motor neurons. Complimentary imaging studies are conducted in pig tissue in order to demonstrate qualitative similarities to human samples. Also, apparent diffusion coefficient (ADC) maps were generated inside porcine α-motor neuron cell bodies and portions of their largest processes (mean=1.7 ± 0.5 μm²/ms based on 53 pixels) as well as in areas containing a mixture of extracellular space, microvasculature, and neuropil (0.59 ± 0.37 μm²/ms based on 33 pixels). Three-dimensional reconstruction of MR images containing α-motor neurons shows the spatial arrangement of neuronal projections between adjacent cells. Such advancements in imaging portend the ability to construct accurate models of MR signal behavior based on direct observation and measurement of the components which comprise functional tissues. These tools would not only be useful for improving our interpretation of macroscopic MRI performed in the clinic, but they could potentially be used to develop new methods of differential diagnosis to aid in the early detection of a multitude of neuropathologies.
磁共振成像(MRI)以其安全生成软组织高对比度图像的无与伦比的能力,一直处于诊断临床医学的前沿。不幸的是,由于分辨率的限制,临床扫描最适用于检测与少数几种病理学相关的宏观结构变化。此外,由于长期以来无法直接观察细胞水平的磁共振(MR)信号行为,因此对这种信息的了解很差,通常必须进行推断。1986 年,MR 显微镜的出现使我们能够测量以前无法观察到的组织结构的 MR 信号特性。最近,硬件技术的进一步改进使得可视化哺乳动物细胞结构成为可能。在当前的研究中,我们通过对人源和猪源α运动神经元的神经元细胞体和突起进行成像,扩展了之前的工作。在猪组织中进行了补充成像研究,以证明与人样本的定性相似性。此外,还在猪α运动神经元细胞体内部及其最大突起的一部分(基于 53 个像素的平均为 1.7 ± 0.5 μm²/ms)以及包含细胞外空间、微血管和神经胶质的区域(基于 33 个像素的平均为 0.59 ± 0.37 μm²/ms)生成了表观扩散系数(ADC)图。包含α运动神经元的 MR 图像的三维重建显示了相邻细胞之间神经元突起的空间排列。这些成像方面的进展预示着能够根据组成功能组织的组件的直接观察和测量来构建准确的 MR 信号行为模型。这些工具不仅有助于提高我们对临床进行的宏观 MRI 的解释,而且它们还有可能被用于开发新的鉴别诊断方法,以帮助早期发现多种神经病理学。