Immunohistochemical study of pseudohypertrophy of the inferior olivary nucleus

Clin Neuropathol. 2014 Jan-Feb;33(1):68-75. doi: 10.5414/NP300594.

Abstract

Objective: Pathogenesis of pseudohypertrophy of the inferior olivary nucleus (PH-IO) was analyzed based on immunohistochemical study.

Methods: Immunostained medullas with PH-IO were observed with confocal laser microscopy.

Results: αB-crystallin (αBC) was frequently expressed in the neurons and co-localized with microtubule-associated protein 2 (MAP2). The neurons were occasionally positive for SMI-31. αBC and SMI-31 were co-localized in some neurons. Synaptophysin (SYP)-immunoreactive dots were present around MAP2-positive hypertrophic neurons and hypertrophic thick neurites. Periphery-stained Lys-Asp-Glu-Leu (KDEL)-positive neurons were shown. Central chromatolytic neurons were found with Klüver-Barrera staining, which indicated that the rough endoplasmic reticulum (ER) was distributed to the periphery of the cytoplasm.

Conclusions: αBC prevents microtubule disassembly and phosphorylation of the neurofilaments under stressful conditions. Our results indicated that αBC protected microtubules and neurofilaments in PH-IO. The retrograde transport of KDEL receptors from the Golgi complex to the ER is increased under stressful conditions. We considered that KDEL receptors were retro-transported to ER, and then the ER containing KDEL receptors was distributed to the periphery of the cytoplasm. PH-IO showed various immunohistochemical changes due to trans-synaptic degeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoplasmic Reticulum / physiology
  • Golgi Apparatus / physiology
  • Humans
  • Hypertrophy / etiology
  • Hypertrophy / metabolism
  • Hypertrophy / pathology
  • Microscopy, Confocal
  • Olivary Nucleus / metabolism*
  • Olivary Nucleus / pathology*
  • Receptors, Peptide / metabolism
  • Retrograde Degeneration / complications
  • Retrograde Degeneration / metabolism
  • Retrograde Degeneration / pathology
  • alpha-Crystallin B Chain / metabolism

Substances

  • KDEL receptor
  • Receptors, Peptide
  • alpha-Crystallin B Chain