Amyloid-β deposits in the cerebral cortex of the aged common marmoset (Callithrix jacchus):: incidence and chemical composition

被引:91
作者
Geula, C
Nagykery, N
Wu, CK
机构
[1] Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Sect Gerontol, Boston, MA 02215 USA
关键词
amyloid; plaques; apolipoprotein E; cholinesterases; common marmoset;
D O I
10.1007/s004010100429
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The incidence, distribution and chemical composition of amyloid-beta (Abeta) peptide-positive deposits were investigated in the lower primate species common marmoset (Callithrix jacchus). No Abeta deposits were observed in the brains of 7 marmosets below 7 years of age. In 15 marmosets above 7 years, 60% displayed cortical Abeta-immunoreactive plaques, 80% had Abeta deposited in intracortical vessels and 87% displayed Abeta deposits in meningeal vessels. The cerebral cortex of the oldest animal (15 years) contained a substantial density of deposits. Abeta-immunoreactive plaques were found predominantly in association cortical zones followed by a lower density in paralimbic cortical areas. Deposits within vessels were most frequent in occipital cortex. Abeta40 was found primarily in vascular deposits, while Abeta42 was present in plaques. Approximately 20% of plaques and most vascular deposits displayed thioflavin S staining, indicative of the presence of fibrillar Abeta. Varying proportions of Abeta deposits contained acetylcholinesterase or butyrylcholinesterase activities and apolipoprotein E and alpha1-antichymotrypsin immunoreactivity. A few plaques contained immunoreactivity for amyloid precursor protein in swollen neurites. However, no abnormally phosphorylated tau immunoreactivity was present in these neurites. Survival analysis in a colony of marmosets indicated that only 6% of animals can be expected to survive beyond 7 years of age. These results indicate that the aged marmoset brain displays Abeta deposits with a distribution and chemical composition similar to those found in the human. These similarities suggest that the aged marmoset may be a useful lower primate model for the study of the pathological effects of Abeta. However, the relatively small number of animals which can be expected to reach old age severely limits the utility of this species as a model of Abeta deposition.
引用
收藏
页码:48 / 58
页数:11
相关论文
共 54 条
[11]   SENILE PLAQUE NEURITES IN ALZHEIMER-DISEASE ACCUMULATE AMYLOID PRECURSOR PROTEIN [J].
CRAS, P ;
KAWAI, M ;
LOWERY, D ;
GONZALEZDEWHITT, P ;
GREENBERG, B ;
PERRY, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7552-7556
[12]   AGGREGATION OF THE AMYLOID PRECURSOR PROTEIN WITHIN DEGENERATING NEURONS AND DYSTROPHIC NEURITES IN ALZHEIMERS-DISEASE [J].
CUMMINGS, BJ ;
SU, JH ;
GEDDES, JW ;
VANNOSTRAND, WE ;
WAGNER, SL ;
CUNNINGHAM, DD ;
COTMAN, CW .
NEUROSCIENCE, 1992, 48 (04) :763-777
[13]   The pathogenesis of senile plaques [J].
Dickson, DW .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (04) :321-339
[14]   THE ACUTE NEUROTOXICITY AND EFFECTS UPON CHOLINERGIC AXONS OF INTRACEREBRALLY INJECTED BETA-AMYLOID IN THE RAT-BRAIN [J].
EMRE, M ;
GEULA, C ;
RANSIL, BJ ;
MESULAM, MM .
NEUROBIOLOGY OF AGING, 1992, 13 (05) :553-559
[15]   ALZHEIMER-TYPE NEUROPATHOLOGY IN TRANSGENIC MICE OVEREXPRESSING V717F BETA-AMYLOID PRECURSOR PROTEIN [J].
GAMES, D ;
ADAMS, D ;
ALESSANDRINI, R ;
BARBOUR, R ;
BERTHELETTE, P ;
BLACKWELL, C ;
CARR, T ;
CLEMENS, J ;
DONALDSON, T ;
GILLESPIE, F ;
GUIDO, T ;
HAGOPIAN, S ;
JOHNSONWOOD, K ;
KHAN, K ;
LEE, M ;
LEIBOWITZ, P ;
LIEBERBURG, I ;
LITTLE, S ;
MASLIAH, E ;
MCCONLOGUE, L ;
MONTOYAZAVALA, M ;
MUCKE, L ;
PAGANINI, L ;
PENNIMAN, E ;
POWER, M ;
SCHENK, D ;
SEUBERT, P ;
SNYDER, B ;
SORIANO, F ;
TAN, H ;
VITALE, J ;
WADSWORTH, S ;
WOLOZIN, B ;
ZHAO, J .
NATURE, 1995, 373 (6514) :523-527
[16]   THE IDENTITY OF THE SEROTONIN-SENSITIVE ARYL ACYLAMIDASE WITH ACETYLCHOLINESTERASE FROM HUMAN-ERYTHROCYTES, SHEEP BASAL GANGLIA AND ELECTRIC-EEL [J].
GEORGE, ST ;
BALASUBRAMANIAN, AS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1980, 111 (02) :511-524
[17]   SPECIAL PROPERTIES OF CHOLINESTERASES IN THE CEREBRAL-CORTEX OF ALZHEIMERS-DISEASE [J].
GEULA, C ;
MESULAM, M .
BRAIN RESEARCH, 1989, 498 (01) :185-189
[18]   Relationship between plaques, tangles, and loss of cortical cholinergic fibers in Alzheimer disease [J].
Geula, C ;
Mesulam, MM ;
Saroff, DM ;
Wu, CK .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1998, 57 (01) :63-75
[19]  
Geula C., 1999, Society for Neuroscience Abstracts, V25, P2052
[20]   CHOLINESTERASES AND THE PATHOLOGY OF ALZHEIMER-DISEASE [J].
GEULA, C ;
MESULAM, MM .
ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 1995, 9 :23-28