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Updated: Jan 15, 2026

In vivo Imaging of the Mouse Spinal Cord Using Two-photon Microscopy
Published on: January 5, 2012
SpIC3D imaging for spinal in situ contrast 3D visualization
Lucy Liang1, Alessandro Fasse2, Arianna Damiani3
1Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA; Rehab Neural Engineering Labs, University of Pittsburgh, Pittsburgh, PA 15213, USA; Center for the Neural Basis of Cognition, Pittsburgh, PA 15213, USA.
Abstract:
High-definition visualization techniques are critical for understanding the neuroanatomy of the spinal cord, an essential structure for sensorimotor and autonomic functions, in both healthy and pathological conditions. Magnetic resonance imaging (MRI) is a common method for visualizing neural structures in 3D. However, techniques for spinal cord MRI have historically achieved limited visualization of rootlets and nerves, especially at lower spinal levels, due to their highly complex and compact organization. Here, we developed a spinal in situ contrast 3D imaging (SpIC3D) method that allows visualization of spinal compartments in fixed animal and human specimens with high resolution (50 μm) at various spinal levels. Using SpIC3D, we achieved quantification of neuronal cell density in dorsal root ganglia, multi-segment identification of individual rootlets and roots, and volumetric reconstruction of multiple spinal structures for computational modeling. SpIC3D provides a basis for accelerated spinal pathology characterization and personalized spinal cord stimulation treatments.
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