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Immunohistochemical characteristics of the constituents of senile plaques and amyloid angiopathy in aged cynomolgus monkeys
- Source :
- Journal of Medical Primatology. 25:294-300
- Publication Year :
- 1996
- Publisher :
- Wiley, 1996.
-
Abstract
- In this study, we immunohistochemically examined the several constituents of senile plaques (SPs) and cerebral amyloid angiopathy (CAA) in aged cynomolgus monkeys. Apolipoprotein E (apoE) deposited in all mature plaques and CAA, and in half of the diffuse plaques. Alpha-1-antichymotripsin (alpha ACT) deposited in half of the mature plaques and in one third of the CAA. Amyloid precursor protein (APP), ubiquitin (Ub), and microtubule-associated protein-2 (MAP-2) accumulated in the swollen neurites of mature plaques. Glial fibrillary acidic protein (GFAP) was detected in the astrocytes and their processes surrounding the mature plaques. Tau was detected in neither the SPs nor CAA. Therefore, mature plaques involved extracellular A beta, apoE, and alpha ACT, and also astrocytes and swollen neurites. However, diffuse plaques involved only extracellular A beta and apoE. Since these features, except for tau, were consistent with those in humans, this animal model will be useful for studying the pathogenesis of cerebral amyloid deposition.
- Subjects :
- Male
Apolipoprotein E
Aging
Pathology
medicine.medical_specialty
alpha 1-Antichymotrypsin
BACE1-AS
Amyloid beta-Protein Precursor
Apolipoproteins E
Glial Fibrillary Acidic Protein
mental disorders
Neurites
medicine
Amyloid precursor protein
Animals
Humans
Senile plaques
Ubiquitins
General Veterinary
biology
Glial fibrillary acidic protein
Chemistry
P3 peptide
Brain
medicine.disease
Immunohistochemistry
Biochemistry of Alzheimer's disease
Cerebral Amyloid Angiopathy
Macaca fascicularis
Astrocytes
biology.protein
Female
Animal Science and Zoology
Cerebral amyloid angiopathy
Microtubule-Associated Proteins
Subjects
Details
- ISSN :
- 00472565
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Journal of Medical Primatology
- Accession number :
- edsair.doi.dedup.....d053c729644c3d31cf3e9825ce1b6e57