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  4. In vivo imaging of the neuronal response to spinal cord injury: a narrative review

In vivo imaging of the neuronal response to spinal cord injury: a narrative review

Neural Regen Res, 2024 · DOI: 10.4103/1673-5374.382225 · Published: April 1, 2024

Spinal Cord InjuryNeurologyMedical Imaging

Simple Explanation

Spinal cord injury (SCI) often causes permanent disability with motor, sensory, and autonomic dysfunction. The neuronal response is key to neural regeneration failure and locomotor dysfunction following SCI. Recent progress in molecular labeling and in vivo imaging approaches has enabled the observation of neuronal dynamics in the healthy and injured CNS. MRI provides macroscopic information about the spatial location of structures, it cannot provide structural information at the cellular or subcellular level to directly observe cell bodies or axons, nor can it evaluate calcium signaling. Two-photon microscopy is a high-resolution imaging technique that uses a focused laser beam to stimulate fluorescent molecules in biological tissues. The functions and locations of spinal sensory neurons and motor neurons are different, and therefore different in vivo imaging approaches are used to study them. Sensory neurons detect and transmit sensory information from the periphery to the spinal cord and brain, and in vivo imaging of sensory neurons often uses genetically encoded calcium indicators (GECIs).

Study Duration
Not specified
Participants
Not specified
Evidence Level
Level 5: Narrative Review

Key Findings

  • 1
    In vivo imaging (especially two-photon microscopy) have provided direct optical access to both the superficial and deep layers of the spinal cord, to explore neuronal and non-neuronal activities of deeper structures in response to behaviors or specific diseases such as SCI.
  • 2
    Spinal cord sensory neuron activity in response to SCI occurs in two places—the neurons in the spinal cord and in the DRG. In SCI, the superficial spinal cord sensory neurons would be directly damaged and then experience swelling, disintegration, and necrosis, whereas the DRG sensory neurons would develop axonal dieback in the spinal cord but their deeper cell bodies could survive.
  • 3
    Within a few weeks of SCI, anterior horn motor neurons may be damaged to varying degrees, including the ventral root. The loss of motor neurons is associated with permanent motor impairment after SCI, and research on anterior horn motor neurons is crucial for understanding the underlying mechanisms of SCI and developing effective therapeutic interventions.

Research Summary

In vivo imaging has the potential to reveal novel mechanisms of neuronal, glial, immune, and vascular responses to SCI in the mammalian CNS. Approaches for repeated in vivo imaging, in vivo imaging of freely behaving mice, and GECI-based in vivo imaging of neuronal activity may all provide greater insights into post-SCI neuronal responses. Molecular information revealed by multi-omics approaches can be used to discover and generate novel molecular probes to detect neuronal dysfunction, immune cell activation, and vascular abnormalities, which have the potential to reveal new avenues for therapeutic intervention in SCI.

Practical Implications

Enhanced Understanding of SCI

In vivo imaging techniques allow for a more detailed understanding of the dynamic biological responses of spinal cord neurons to SCI, aiding in the development of targeted therapies.

Development of Novel Therapies

The application of in vivo imaging can facilitate the testing of transplanted neuron activity and the neuroprotective effects of treatments on SCI, leading to more effective therapeutic interventions.

Improved Diagnostic Accuracy

Advancements in in vivo imaging, such as two-photon microscopy, offer better spatial and temporal resolution for visualizing cellular dynamics, improving the accuracy of SCI diagnosis and monitoring.

Study Limitations

  • 1
    Superficial imaging depth
  • 2
    Movement artifacts during imaging
  • 3
    Immune activation in the spinal cord due to implanted viewing windows

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