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