Long-term in vivo imaging of normal and pathological mouse spinal cord with subcellular resolution using implanted glass windows
J Physiol, 2012 · DOI: 10.1113/jphysiol.2012.230532 · Published: May 28, 2012
Simple Explanation
The study introduces a method for implanting glass windows over the spinal cords of mice. This allows repeated in vivo microscopy without repeated surgeries. The implanted windows remain clear for months and do not damage axons or blood vessels. This makes them useful for studying cellular dynamics after spinal cord injury. The technique enables the tracking of axon degeneration/retraction and regeneration following spinal cord injuries with high temporal resolution.
Key Findings
- 1Implanted glass windows stabilize the spinal cord, reduce motion artifacts, and remain clear for extended periods.
- 2The glass window implantation induces only a transient immune response in the spinal cord.
- 3Regenerating axons can cross a spinal cord injury site within 4 days, with their terminals undergoing morphological changes for weeks afterward.
Research Summary
Practical Implications
Improved Spinal Cord Research
This technique provides a high-throughput, low-cost method for studying spinal cord physiology and pathology over extended periods with high temporal fidelity.
Therapeutic Evaluation
The method can be used to assess the efficacy and target selectivity of new therapeutic molecules for spinal cord injuries and diseases in real-time.
Cell Graft Tracking
The glass window technique facilitates the tracking of grafted cells in cell graft therapies, helping to clarify the mechanisms responsible for their beneficial effects.
Study Limitations
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