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  4. Developmental expression and function analysis of protein tyrosine phosphatase receptor type D in oligodendrocyte myelination

Developmental expression and function analysis of protein tyrosine phosphatase receptor type D in oligodendrocyte myelination

Neuroscience, 2015 · DOI: 10.1016/j.neuroscience.2015.08.062 · Published: November 12, 2015

NeurologyGenetics

Simple Explanation

This study investigates the role of PTPRD, a protein found in the central nervous system, in the myelination process. Myelination is crucial for nerve function. The research found that PTPRD is expressed in mature neurons and oligodendrocytes, cells responsible for myelination. Mutant mice lacking PTPRD showed a temporary delay in myelination during early development. The study also examined the role of PTPRD in remyelination after induced demyelination. The absence of PTPRD did not affect the remyelination process, suggesting it is not essential for this.

Study Duration
Not specified
Participants
Wild-type and PTPRD mutant mice
Evidence Level
Not specified

Key Findings

  • 1
    PTPRD is initially expressed in mature neurons in the embryonic CNS and later in oligodendroglial cells at postnatal stages.
  • 2
    In PTPRD mutants, oligodendrocyte differentiation was normal, but a transient myelination delay occurred at early postnatal stages.
  • 3
    The remyelination process was not affected in the absence of PTPRD function after cuprizone-induced demyelination in adult animals.

Research Summary

The study examines the expression and function of PTPRD in oligodendrocyte myelination. PTPRD is expressed in mature neurons early in development and later in oligodendrocytes during active myelination. PTPRD mutants showed a transient delay in myelination, but oligodendrocyte differentiation was normal. This suggests PTPRD contributes to the initiation of axonal myelination. Remyelination was unaffected in PTPRD mutants after induced demyelination, indicating PTPRD is not essential for remyelination.

Practical Implications

Targeted Therapies

Understanding the role of PTPRD in myelination could lead to targeted therapies for demyelinating diseases.

Developmental Milestones

The transient myelination delay suggests PTPRD is important during specific developmental windows for myelination initiation.

Redundancy Exploration

The mild phenotype in PTPRD mutants suggests the need to explore functional redundancy with other RPTP family members.

Study Limitations

  • 1
    Possible functional redundancy from other related molecules
  • 2
    Mild phenotype in axonal myelination
  • 3
    The study focused on cuprizone-induced demyelination, which may not fully represent other demyelinating conditions.

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