Aberrant neuronal-glial differentiation in Taylor-type focal cortical dysplasia (type IIA/B)

Acta Neuropathol. 2005 May;109(5):519-33. doi: 10.1007/s00401-005-1005-9. Epub 2005 May 5.

Abstract

Focal cortical dysplasia (FCD) type IIA/B (Taylor type) is a malformation of cortical development characterized by laminar disorganization and dysplastic neurons. FCD IIA and FCD IIB denote subtypes in which balloon cells are absent or present, respectively. The etiology of FCD IIA/B is unknown, but previous studies suggest that its pathogenesis may involve aberrant, mixed neuronal-glial differentiation. To investigate whether aberrant differentiation is a consistent phenotype in FCD IIA/B, we studied a panel of neuronal and glial marker antigens in a series of 15 FCD IIB cases, and 2 FCD IIA cases. Double-labeling immunofluorescence and confocal imaging revealed that different combinations of neuronal and glial antigens were co-expressed by individual cells in all cases of FCD IIA/B, but not in control cases of epilepsy due to other causes. Co-expression of neuronal and glial markers was most common in balloon cells, but was also observed in dysplastic neurons. The relative expression of neuronal and glial antigens varied over a broad range. Microtubule-associated protein 1B, an immature neuronal marker, was more frequently co-expressed with glial antigens than were mature neuronal markers, such as neuronal nuclear antigen. Our results indicate that aberrant neuronal-glial differentiation is a consistent and robust phenotype in FCD IIA/B, and support the hypothesis that developmental defects of neuronal and glial fate specification play an important role in its pathogenesis.

Publication types

  • Clinical Conference
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cell Count / methods
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology*
  • Child
  • Child, Preschool
  • Female
  • Fluorescent Antibody Technique / methods
  • Glial Fibrillary Acidic Protein / metabolism
  • Humans
  • Indoles / metabolism
  • Male
  • Microtubule-Associated Proteins / metabolism
  • Middle Aged
  • Nervous System Malformations / metabolism
  • Nervous System Malformations / pathology*
  • Neurofilament Proteins / metabolism
  • Neuroglia / classification
  • Neuroglia / metabolism
  • Neuroglia / pathology*
  • Neurons / classification
  • Neurons / metabolism
  • Neurons / pathology*
  • Phenotype
  • Phosphopyruvate Hydratase / metabolism
  • S100 Proteins / metabolism
  • Staining and Labeling / methods

Substances

  • Glial Fibrillary Acidic Protein
  • Indoles
  • MAP2 protein, human
  • Microtubule-Associated Proteins
  • Neurofilament Proteins
  • S100 Proteins
  • microtubule-associated protein 1B
  • neurofilament protein H
  • DAPI
  • Phosphopyruvate Hydratase