Immunohistochemical study of apolipoprotein E in human cerebrovascular white matter lesions

Hidekazu Tomimoto, Ichiro Akiguchi, Toshihiko Suenaga, Hideaki Wakita, Shinichi Nakamura, Jun Kimura, Herbert Budka

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

In the brains of nine cases with cerebrovascular disease, one with mixed dementia, one with amyloid angiopathy and two non-neurological controls, we found three cases with focal accumulation of apolipoprotein E (apo-E) in dystrophic axons and accompanying macrophages. Since amyloid precursor protein (APP) and chromogranin A (CgA) accumulate after axonal damages, and are sensitive markers of the white matter lesions, the regional distribution of apo-E was compared to that of APP and CgA. apo-E-immunoreactive axons were present in the periphery of an infarction with neighboring macrophages, but not in mild white matter lesions that contained APP- or CgA-immunoreactive fiber bundles. The results suggest a role of apo-E in recycling cholesterol and other membrane components via macrophages into remodeling neurites in the brain, but this phenomenon is restricted to the periphery of infarction and may be less prominent than in the peripheral nervous system.

Original languageEnglish
Pages (from-to)608-614
Number of pages7
JournalActa Neuropathologica
Volume90
Issue number6
DOIs
Publication statusPublished - 01-12-1995
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

Fingerprint Dive into the research topics of 'Immunohistochemical study of apolipoprotein E in human cerebrovascular white matter lesions'. Together they form a unique fingerprint.

  • Cite this

    Tomimoto, H., Akiguchi, I., Suenaga, T., Wakita, H., Nakamura, S., Kimura, J., & Budka, H. (1995). Immunohistochemical study of apolipoprotein E in human cerebrovascular white matter lesions. Acta Neuropathologica, 90(6), 608-614. https://doi.org/10.1007/BF00318573