Mechanisms and time course of neuronal degeneration in experimental autoimmune encephalomyelitis

Muriel Hobom*, Maria K. Storch, Robert Weissert, Katharina Maier, Anand Radhakrishnan, Birgit Kramer, Mathias Bähr, Ricarda Diem

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

133 Scopus citations

Abstract

Neuronal and axonal damage is considered to be the main cause for long-term disability in multiple sclerosis. We analyzed the mechanisms and kinetics of neuronal cell death in experimental autoimmune encephalomyelitis (EAE) induced by myelin oligodendrocyte glycoprotein (MOG) by combining an electrophysiological in vivo assessment of the optic pathway with the investigation of retinal ganglion cell (RGC) counts. In accordance with our previous findings in this animal model, neuritis of the optic nerve (ON) leads to apoptotic RGC death. By further investigating the time course of RGC apoptosis in the present study, we found that neuronal cell death together with decreased visual acuity values occurred before the onset of clinical symptoms. Simultaneously with the time course of RGC apoptosis, we found a down-regulation of phospho-Akt as well as a shift in the relation of 2 proteins of the Bcl-2 family, Bax and Bcl-2, towards a more proapoptotic ratio in these cells. Comparing the kinetics and mechanisms of RGC death during MOG-EAE with those following complete surgical transection of the ON, we found significant agreement. We hypothesize that the main reason for RGC loss in MOG-EAE is the inflammatory attack but RGC death also occurs independently of histopathological ON changes.

Original languageEnglish (US)
Pages (from-to)148-157
Number of pages10
JournalBrain Pathology
Volume14
Issue number2
StatePublished - Apr 2004
Externally publishedYes

ASJC Scopus subject areas

  • Neuroscience(all)
  • Pathology and Forensic Medicine

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