Altered Expression of Astrocyte-Related Receptors and Channels Correlates With Epileptogenesis in Hippocampal Sclerosis

Pediatr Dev Pathol. 2019 Nov-Dec;22(6):532-539. doi: 10.1177/1093526619855488. Epub 2019 Jun 5.

Abstract

Background: Hippocampal sclerosis (HS) is one of the major causes of intractable epilepsy. Astrogliosis in epileptic brain is a peculiar condition showing epileptogenesis and is thought to be different from the other pathological conditions. The aim of this study is to investigate the altered expression of astrocytic receptors, which contribute to neurotransmission in the synapse, and channels in HS lesions.

Methods: We performed immunohistochemical and immunoblotting analyses of the P2RY1, P2RY2, P2RY4, Kir4.1, Kv4.2, mGluR1, and mGluR5 receptors and channels with the brain samples of 20 HS patients and 4 controls and evaluated the ratio of immunopositive cells and those expression levels.

Results: The ratio of each immunopositive cell per glial fibrillary acidic protein-positive astrocytes and the expression levels of all 7 astrocytic receptors and channels in HS lesions were significantly increased. We previously described unique astrogliosis in epileptic lesions similar to what was observed in this study.

Conclusion: This phenomenon is considered to trigger activation of the related signaling pathways and then contribute to epileptogenesis. Thus, astrocytes in epileptic lesion may show self-hyperexcitability and contribute to epileptogenesis through the endogenous astrocytic receptors and channels. These findings may suggest novel astrocytic receptor-related targets for the pharmacological treatment of epilepsy.

Keywords: astrocyte; epilepsy; hippocampal sclerosis; metabotropic receptor; potassium channels; purinergic receptor.

MeSH terms

  • Adolescent
  • Adult
  • Astrocytes / metabolism*
  • Biomarkers / metabolism
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Epilepsy / etiology*
  • Epilepsy / metabolism
  • Epilepsy / pathology
  • Hippocampus / metabolism
  • Hippocampus / pathology*
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Male
  • Potassium Channels / metabolism*
  • Receptors, Metabotropic Glutamate / metabolism*
  • Receptors, Purinergic P2Y / metabolism*
  • Sclerosis
  • Signal Transduction
  • Up-Regulation
  • Young Adult

Substances

  • Biomarkers
  • Potassium Channels
  • Receptors, Metabotropic Glutamate
  • Receptors, Purinergic P2Y