Reelin immunoreactivity in neuritic varicosities in the human hippocampal formation of non-demented subjects and Alzheimer's disease patients

Acta Neuropathol Commun. 2013 Jun 26:1:27. doi: 10.1186/2051-5960-1-27.

Abstract

Background: Reelin and its downstream signaling members are important modulators of actin and microtubule cytoskeleton dynamics, a fundamental prerequisite for proper neurodevelopment and adult neuronal functions. Reductions in Reelin levels have been suggested to contribute to Alzheimer's disease (AD) pathophysiology. We have previously reported an age-related reduction in Reelin levels and its accumulation in neuritic varicosities along the olfactory-limbic tracts, which correlated with cognitive impairments in aged mice. Here, we aimed to investigate whether a similar Reelin-associated neuropathology is observed in the aged human hippocampus and whether it correlated with dementia status.

Results: Our immunohistochemical stainings revealed the presence of N- and C-terminus-containing Reelin fragments in corpora amylacea (CAm), aging-associated spherical deposits. The density of these deposits was increased in the molecular layer of the subiculum of AD compared to non-demented individuals. Despite the limitation of a small sample size, our evaluation of several neuronal and glial markers indicates that the presence of Reelin in CAm might be related to aging-associated impairments in neuronal transport leading to accumulation of organelles and protein metabolites in neuritic varicosities, as previously suggested by the findings and discussions in rodents and primates.

Conclusions: Our results indicate that aging- and disease-associated changes in Reelin levels and proteolytic processing might play a role in the formation of CAm by altering cytoskeletal dynamics. However, its presence may also be an indicator of a degenerative state of neuritic compartments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged, 80 and over
  • Alzheimer Disease / cerebrospinal fluid
  • Alzheimer Disease / metabolism*
  • Astrocytes / metabolism
  • Blotting, Western
  • Cell Adhesion Molecules, Neuronal / cerebrospinal fluid
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Extracellular Matrix Proteins / cerebrospinal fluid
  • Extracellular Matrix Proteins / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Hippocampus / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Microglia / metabolism
  • Nerve Tissue Proteins / cerebrospinal fluid
  • Nerve Tissue Proteins / metabolism*
  • Neurons / metabolism*
  • Reelin Protein
  • Serine Endopeptidases / cerebrospinal fluid
  • Serine Endopeptidases / metabolism*

Substances

  • Cell Adhesion Molecules, Neuronal
  • Extracellular Matrix Proteins
  • Nerve Tissue Proteins
  • Reelin Protein
  • RELN protein, human
  • Reln protein, mouse
  • Serine Endopeptidases