Acta Neuropathologica

, Volume 89, Issue 4, pp 356–362 | Cite as

Distribution of neuronal growth-promoting factors and cytoskeletal proteins in altered neurites in Alzheimer's disease and non-demented elderly

  • Shan-Shan Zhan
  • Wouter Kamphorst
  • William E. Van Nostrand
  • Piet Eikelenboom
Regular Paper

Abstract

In the present immunohistochemical study, we investigated the characteristics of altered neurites in the frontal cortex of 10 Alzheimer's disease (AD) brains and 15 age-matched non-demented control brains. In both AD and control cases, the altered neurites in coronas of the classical plaques (CP) were frequently immunostained by antibodies to growth-promoting factors, N and C termini of amyloid precursor protein (APP), GAP43, collagen IV, laminin and the integrin receptor VLA6. The altered neurites in CP coronas in AD but not in controls were also immunostained by antibodies against normally and abnormally phosphorylated tau. Immunolabeling for microtubule-associated protein 2 was not found in CP from either group. Extensive neuropil threads (NT) and many neurofibrillary tangles (NFT), immunostained with tau and Alz50 antibodies, were present in AD neocortex but not seen in control cases. NT and NFT could not be stained by antibodies to the N termini of APP, GAP43, collagen IV, laminin and VLA6. Our findings indicate that in AD cases altered neurites in CP are undergoing both an aberrant sprouting process and a degenerating process. These altered neurites are probably of axon origin. NT and NFT may represent destructive changes. The presence of amyloid plaques, but absence of tau-related cytoskeletal pathology, in non-demented cases suggests that β/A4 peptide is necessary but not sufficient to induce neurofibrillary pathology.

Key words

Alzheimer's disease Altered neurites Neuropil threads Growth-promoting factors Tau-related cytoskeletal pathology 

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Copyright information

© Springer-Verlag 1995

Authors and Affiliations

  • Shan-Shan Zhan
    • 1
    • 2
  • Wouter Kamphorst
    • 1
  • William E. Van Nostrand
    • 3
  • Piet Eikelenboom
    • 2
  1. 1.Department of NeuropathologyFree University HospitalAmsterdamThe Netherlands
  2. 2.Department of Psychiatry, Medical FacultyFree UniversityAmsterdamThe Netherlands
  3. 3.Department of Microbiology and Molecular Genetics, College of MedicineUniversity of CaliforniaIrvineUSA

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