Glial hyaluronate-binding protein in dysmyelinating mice mutants: jimpy, quaking and shiverer

A Bignami1, G Perides

  • 1Department of Pathology, Harvard Medical School, West Roxbury, MA.

Acta Neuropathologica
|January 1, 1989
PubMed

Insights

Glial hyaluronate-binding protein (GHAP) expression in astrocytes is independent of myelination. This study reveals white matter astrocytes are a distinct glial cell population.

Area of Science:

  • Neuroscience
  • Cell Biology
  • Biochemistry

Background:

  • Glial hyaluronate-binding protein (GHAP) is a brain-specific extracellular matrix glycoprotein produced by astrocytes.
  • Its distribution in normal mammalian brains is primarily in white matter, with an exception in the granular layer of the cerebellum.

Purpose of the Study:

  • To investigate the relationship between GHAP expression and myelination in the central nervous system.
  • To determine if GHAP expression is induced by the myelination process.
  • To characterize white matter astrocytes as a distinct glial population.

Main Methods:

  • Indirect immunofluorescence staining of cryostat sections from cerebral hemispheres, cerebellum, and spinal cord of dysmyelinating mouse mutants (quaking, jimpy, shiverer) and littermate controls.
  • Utilized polyclonal antibodies against GHAP and glial fibrillary acidic protein (GFAP).

Main Results:

  • GHAP distribution in normal mice mirrored previously reported findings in various mammalian species.
  • No significant differences in GHAP localization were observed between mutant mice and their littermate controls.
  • A denser glial framework was noted in mutants compared to controls when stained for both GHAP and GFAP, likely due to reduced myelin.

Conclusions:

  • GHAP expression in astrocytes is not dependent on or induced by myelination.
  • These findings support the concept that white matter astrocytes represent a distinct population of glial cells within the brain.

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