Alterations of Hippocampal Myelin Sheath and Axon Sprouting by Status Convulsion and Regulating Lingo-1 Expression with RNA Interference in Immature and Adult Rats

Neurochem Res. 2018 Mar;43(3):721-735. doi: 10.1007/s11064-018-2474-2. Epub 2018 Jan 27.

Abstract

Seizure-induced brain damage is age-dependent, as evidenced by the different alterations of neural physiopathology in developing and mature brains. However, little is known about the age-dependent characteristics of myelinated fiber injury induced by seizures. Considering the critical functions of oligodendrocyte progenitor cells (OPCs) in myelination and Lingo-1 signaling in regulating OPCs' differentiation, the present study aimed to explore the effects of Lingo-1 on myelin and axon in immature and adult rats after status convulsion (SC) induced by lithium-pilocarpine, and the differences between immature and adult brains. Dynamic variations in electrophysiological activity and spontaneous recurrent seizures were recorded by electroencephalogram monitoring after SC. The impaired microstructures of myelin sheaths and decrease in myelin basic protein caused by SC were observed through transmission electron microscopy and western blot analysis respectively, which became more severe in adult rats, but improved gradually in immature rats. Aberrant axon sprouting occurred in adult rats, which was more prominent than in immature rats, as shown by a Timm stain. This damage was improved or negatively affected after down or upregulating Lingo-1 expression. These results demonstrated that in both immature and adult brains, Lingo-1 signaling plays important roles in seizure-induced damage to myelin sheaths and axon growth. The plasticity of the developing brain may provide a potential window of opportunity to prevent the brain from damage.

Keywords: Age-dependent damage; Mossy fiber sprouting; Myelin sheath; Oligodendrocyte progenitor cells; Status convulsion.

MeSH terms

  • Age Factors
  • Animals
  • Axons / metabolism*
  • Axons / pathology
  • Cell Differentiation / drug effects
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Membrane Proteins / metabolism*
  • Myelin Sheath / metabolism*
  • Nerve Tissue Proteins / metabolism*
  • Oligodendroglia / metabolism
  • RNA Interference / physiology
  • Rats, Sprague-Dawley
  • Seizures / metabolism*

Substances

  • LINGO1 protein, rat
  • Membrane Proteins
  • Nerve Tissue Proteins