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Magnetic Resonance Microscopy of Human and Porcine Neurons and Cellular Processes

Overview
Journal Neuroimage
Specialty Radiology
Date 2012 Jan 28
PMID 22281672
Citations 20
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Abstract

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.

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References
1.
Ehrmann K, Saillen N, Vincent F, Stettler M, Jordan M, Wurm F . Microfabricated solenoids and Helmholtz coils for NMR spectroscopy of mammalian cells. Lab Chip. 2007; 7(3):373-80. DOI: 10.1039/b614044k. View

2.
Massin C, Vincent F, Homsy A, Ehrmann K, Boero G, Besse P . Planar microcoil-based microfluidic NMR probes. J Magn Reson. 2003; 164(2):242-55. DOI: 10.1016/s1090-7807(03)00151-4. View

3.
Szafer A, Zhong J, Gore J . Theoretical model for water diffusion in tissues. Magn Reson Med. 1995; 33(5):697-712. DOI: 10.1002/mrm.1910330516. View

4.
Meadowcroft M, Zhang S, Liu W, Park B, Connor J, Collins C . Direct magnetic resonance imaging of histological tissue samples at 3.0T. Magn Reson Med. 2007; 57(5):835-41. PMC: 4040526. DOI: 10.1002/mrm.21213. View

5.
Hansen B, Flint J, Heon-Lee C, Fey M, Vincent F, King M . Diffusion tensor microscopy in human nervous tissue with quantitative correlation based on direct histological comparison. Neuroimage. 2011; 57(4):1458-65. PMC: 3138905. DOI: 10.1016/j.neuroimage.2011.04.052. View