Histopathological studies of senile plaques and cerebral amyloidosis in cynomolgus monkeys

被引:68
作者
Nakamura, S
Nakayama, H
Goto, N
Ono, F
Sakakibara, I
Yoshikawa, Y
机构
[1] Univ Tokyo, Fac Agr, Dept Biomed Sci, Bunkyo Ku, Tokyo 113, Japan
[2] Univ Tokyo, Fac Agr, Dept Vet Pathol, Bunkyo Ku, Tokyo 113, Japan
[3] Natl Inst Hlth, Tsukuba Primate Ctr Med Sci, Tsukuba, Ibaraki 305, Japan
关键词
aging; Alzheimer's disease; amyloid angiopathy; amyloid beta protein;
D O I
10.1111/j.1600-0684.1998.tb00244.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Senile plaques (SPs) and cerebral amyloid angiopathy (CAA), pathological hallmarks of Alzheimer's disease, have not been thoroughly investigated histopathologically in nonhuman primates. To determine the onset age and histopathological characteristics of SPs and CAA, we-examined the brains of 64 cynomolgus monkeys (Macaca fascicularis) from 2 to 35 years old. Mature (classical and primitive) plaques appeared in 16 out of 25 monkeys that were >20 years old. Moreover, mature plaques were observed more frequently than diffuse plaques and were located in the temporal cortex of the superior or inferior gyri and amygdala. Diffuse plaques in contrast to mature plaques did not show definite tendencies in onset age and distribution. CAA appeared in more than 22-year-old monkeys in 10 out of 16 animals and was frequently observed in capillaries and often found adjoining mature plaques. During immunohistochemical examination, an antiserum for amyloid beta protein (A beta) 1-40 could detect all SPs, whereas a monoclonal antibody for A beta 8-17 could not detect any diffuse plaques and only one third of the primitive plaques, As for CAA, the polyclonal antiserum was more sensitive than the monoclonal antibody. The present study describes the histopathological features of SPs and CAA in old cynomolgus monkeys.
引用
收藏
页码:244 / 252
页数:9
相关论文
共 32 条
[1]  
ALIAVINI F, 1988, NEUROSCI LETT, V93, P191
[2]   IDENTIFICATION OF AMYLOID-BETA PROTEIN IN THE BRAIN OF THE SMALL, SHORT-LIVED LEMURIAN PRIMATE MICROCEBUS-MURINUS [J].
BONS, N ;
MESTRE, N ;
RITCHIE, K ;
PETTER, A ;
PODLISNY, M ;
SELKOE, D .
NEUROBIOLOGY OF AGING, 1994, 15 (02) :215-220
[3]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[4]   NEUROPATHOLOGY AND APOLIPOPROTEIN-E PROFILE OF AGED CHIMPANZEES - IMPLICATIONS FOR ALZHEIMER-DISEASE [J].
GEARING, M ;
REBECK, GW ;
HYMAN, BT ;
TIGGES, J ;
MIRRA, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9382-9386
[5]   CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF A CDNA-ENCODING BRAIN AMYLOID OF ALZHEIMERS-DISEASE [J].
GOLDGABER, D ;
LERMAN, MI ;
MCBRIDE, OW ;
SAFFIOTTI, U ;
GAJDUSEK, DC .
SCIENCE, 1987, 235 (4791) :877-880
[6]   Co-localization of beta-amyloid peptides, apolipoprotein E and glial markers in senile plaques in the prefrontal cortex of old rhesus monkeys [J].
Hartig, W ;
Bruckner, G ;
Schmidt, C ;
Brauer, K ;
Bodewitz, G ;
Turner, JD ;
Bigl, V .
BRAIN RESEARCH, 1997, 751 (02) :315-322
[7]  
HONJO S, 1985, J MED PRIMATOL, V14, P75
[8]   VISUALIZATION OF A-BETA-42(43) AND A-BETA-40 IN SENILE PLAQUES WITH END-SPECIFIC A-BETA MONOCLONALS - EVIDENCE THAT AN INITIALLY DEPOSITED SPECIES IS A-BETA-42(43) [J].
IWATSUBO, T ;
ODAKA, A ;
SUZUKI, N ;
MIZUSAWA, H ;
NUKINA, N ;
IHARA, Y .
NEURON, 1994, 13 (01) :45-53
[9]  
KITAMOTO T, 1987, LAB INVEST, V57, P230
[10]   NUCLEOTIDE-SEQUENCE OF THE CYNOMOLGUS MONKEY APOLIPOPROTEIN-E CDNA [J].
MAROTTI, KR ;
WHITTED, BE ;
CASTLE, CK ;
POLITES, HG ;
MELCHIOR, GW .
NUCLEIC ACIDS RESEARCH, 1989, 17 (04) :1778-1778