Neurofibrillary Tangles and the Deposition of a Beta Amyloid Peptide with a Novel N-Terminal Epitope in the Brains of Wild Tsushima Leopard Cats

被引:25
作者
Chambers, James K. [1 ]
Uchida, Kazuyuki [1 ]
Harada, Tomoyuki [1 ]
Tsuboi, Masaya [1 ]
Sato, Masumi [2 ]
Kubo, Masahito [3 ]
Kawaguchi, Hiroaki [4 ]
Miyoshi, Noriaki [4 ]
Tsujimoto, Hajime [5 ]
Nakayama, Hiroyuki [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Vet Pathol, Tokyo, Japan
[2] Natl Inst Anim Hlth, Ibaraki, Japan
[3] Yamaguchi Univ, Joint Fac Vet Med, Lab Vet Pathol, Yamaguchi, Japan
[4] Kagoshima Univ, Lab Vet Histopathol, Joint Fac Vet Med, Kagoshima 890, Japan
[5] Univ Tokyo, Dept Vet Internal Med, Grad Sch Agr & Life Sci, Tokyo, Japan
来源
PLOS ONE | 2012年 / 7卷 / 10期
基金
日本学术振兴会;
关键词
SENILE PLAQUES; ALZHEIMERS-DISEASE; TAU-PROTEIN; A-BETA; NEURODEGENERATIVE DISEASES; ANIMAL-MODELS; MOUSE MODEL; OLIGOMERS; PATHOLOGY; ACCUMULATION;
D O I
10.1371/journal.pone.0046452
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Beta amyloid (A beta) deposits are seen in aged individuals in many of the mammalian species that possess the same Ab amino acid sequence as humans. Conversely, neurofibrillary tangles (NFT), the other hallmark lesion of Alzheimer's disease (AD), are extremely rare in these animals. We detected Ab deposits in the brains of Tsushima leopard cats (Prionailurus bengalensis euptilurus) that live exclusively on Tsushima Island, Japan. A beta 42 was deposited in a granular pattern in the neuropil of the pyramidal cell layer, but did not form argyrophilic senile plaques. These Ab deposits were not immunolabeled with antibodies to the N-terminal of human A beta. Sequence analysis of the amyloid precursor protein revealed an amino acid substitution at the 7th residue of the A beta peptide. In a comparison with other mammalian animals that do develop argyrophilic senile plaques, we concluded that the alternative A beta amino acid sequence displayed by leopard cats is likely to be related to its distinctive deposition pattern. Interestingly, most of the animals with these A beta deposits also developed NFTs. The distributions of hyperphosphorylated tau-positive cells and the two major isoforms of aggregated tau proteins were quite similar to those seen in Alzheimer's disease. In addition, the unphosphorylated form of GSK-3 beta colocalized with hyperphosphorylated tau within the affected neurons. In conclusion, this animal species develops AD-type NFTs without argyrophilic senile plaques.
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页数:10
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