NEUROFIBRILLARY TANGLES AND SENILE PLAQUES IN AGED BEARS

被引:121
作者
CORK, LC
POWERS, RE
SELKOE, DJ
DAVIES, P
GEYER, JJ
PRICE, DL
机构
[1] JOHNS HOPKINS UNIV, SCH MED, DEPT PSYCHIAT & BEHAV SCI, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROL, BALTIMORE, MD 21205 USA
[3] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROSCI, BALTIMORE, MD 21205 USA
[4] HARVARD UNIV, SCH MED, DEPT NEUROL NEUROSCI, BOSTON, MA 02115 USA
[5] BRIGHAM & WOMENS HOSP, CTR NEUROL DIS, BOSTON, MA 02115 USA
[6] YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT PATHOL, BRONX, NY 10461 USA
关键词
D O I
10.1097/00005072-198811000-00006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In aged human beings and in individuals with age-associated degenerative disorders, particularly Alzheimer''s disease (AD), neurons develop cytoskeletal abnormalities, including neurofibrillary tangles (NFT) and senile plaques (SP). Senile plaques occur in several nonhuman species; however, NFT, with ultrastructural or immunocytochemical similarities to those occurring in humans, have not been identified in other mammals. In this study of five aged bears (Ursus, 20-30 years of age), we identified cytoskeletal abnormalities similar to those occurring in humans. An aged Asiatic brown bear had NFT, composed of straight 10-16-nm filaments, that were immunoreactive with antibodies directed against: phosphorylated epitopes of neurofilaments (NF); tau; A68 (a protein enriched in AD); and an antigen associated with paired helical filaments (PHF). An aged polar bear had numerous SP; neurites of these plaques were immunoreactive with antibodies against phosphorylated epitopes of NF, but NFT were not identified. These results indicate that nonprimate species develope age-related cytoskeletal abnormalities similar to those occurring in humans. Investigations of the comparative pathology of aged mammals may be useful in elucidating the pathogeneses of these abnormalities.
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页码:629 / 641
页数:13
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