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  4. Age-related myelin dynamics revealed by increased oligodendrogenesis and short internodes

Age-related myelin dynamics revealed by increased oligodendrogenesis and short internodes

Aging Cell, 2009 · DOI: 10.1111/j.1474-9726.2009.00462.x · Published: April 1, 2009

AgingNeurology

Simple Explanation

This study investigates how myelin, a protective sheath around nerve fibers, changes with age in the spinal cord of mice. The researchers found that as mice age, the length of myelin segments (internodes) decreases, suggesting the spinal cord is actively trying to repair myelin. The study also looked at the production of new glial cells, which support nerve cells. They observed an increase in the generation of oligodendrocytes, cells that produce myelin, in the white matter of older mice, further supporting the idea of ongoing myelin repair. Interestingly, the study found that new astrocytes, another type of glial cell, were rarely produced. This suggests that the aging spinal cord prioritizes the production of myelin-producing cells to maintain or repair nerve fiber insulation.

Study Duration
2.5, 14 and 21 months
Participants
C57Bl/6 female mice
Evidence Level
Not specified

Key Findings

  • 1
    Internode lengths of rubrospinal tract axons significantly decrease with age, suggesting active remyelination.
  • 2
    Gliogenesis increases in the white matter of the spinal cord in older mice (21 months).
  • 3
    Newly generated cells primarily differentiate into oligodendrocytes, with limited differentiation into astrocytes.

Research Summary

This study characterized myelin changes within the murine rubrospinal tract and found that internode lengths significantly decrease as a function of age which suggests active remyelination. The data reveal a decrease in glial cell proliferation from 1 to 6, 14 and 21 months of age in gray matter 4 weeks post BrdU injections. However, we found an increase in gliogenesis at 21 months in white matter of the spinal cord. These data demonstrate ongoing oligodendrogenesis and myelinogenesis as a function of age in the spinal cord.

Practical Implications

Understanding Normal Aging

Provides a baseline understanding of myelin maintenance and glial cell turnover in the normal aging murine spinal cord, which can help differentiate normal aging changes from those caused by disease.

Potential Therapeutic Targets

Suggests that promoting oligodendrogenesis could be a potential therapeutic strategy for addressing myelin-related decline in aging or neurological disorders.

Implications for Spinal Cord Injury/MS

Findings related to cell proliferation shifts may have ramifications for therapeutic applications of drugs or cell transplants after spinal cord injury or MS.

Study Limitations

  • 1
    The study is limited to the murine rubrospinal tract; findings may not be generalizable to other CNS regions.
  • 2
    The study focuses on anatomical changes; functional consequences of short internodes are not directly assessed.
  • 3
    The use of BrdU to track cell proliferation has limitations, including potential signal dilution and the inability to rule out apoptosis.

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