BASIC FIBROBLAST GROWTH-FACTOR BINDING IS A MARKER FOR EXTRACELLULAR NEUROFIBRILLARY TANGLES IN ALZHEIMER-DISEASE

被引:56
作者
SIEDLAK, SL [1 ]
CRAS, P [1 ]
KAWAI, M [1 ]
RICHEY, P [1 ]
PERRY, G [1 ]
机构
[1] CASE WESTERN RESERVE UNIV,INST PATHOL,DIV NEUROPATHOL,2085 ADELBERT RD,CLEVELAND,OH 44106
关键词
HEPARAN SULFATE PROTEOGLYCAN; EXTRACELLULAR MATRIX; PROTEOGLYCAN; NEUROFIBRILLARY PATHOLOGY; AMYLOID;
D O I
10.1177/39.7.1865106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neurofibrillary tangles (NFT) are abnormal filamentous inclusions that develop in neurons in Alzheimer disease and other disorders. When neurons die, the neurofibrillary tangles that persist in the extracellular space show ultrastructural and antigenic changes. Both intra- and extracellular NFT have recently been shown to contain heparan sulfate proteoglycans (HSPGs). HSPGs are also present in other amyloid deposits in the brain and in systemic amyloidoses. Basic fibroblast growth factor (bFGF) is a heparin binding growth factor which is involved in angiogenesis and also has neurite promoting activity. We now report that bFGF binds avidly to extracellular NFT. Alz-50, a monoclonal antibody (MAb) to an abnormal form of tau and bFGF binding label mutually exclusive subpopulations of neurofibrillary tangles. bFGF binding is abolished by heparinase or heparitinase treatment and therefore is most likely based on the presence of HSPG. Binding of bFGF is a specific and sensitive morphological method to distinguish intra- from extracellular NFT. As intracellular NFT, which also contain HSPGs, are not labeled by bFGF binding, this finding also suggests that HSPGs are modified when the NFT become extracellular.
引用
收藏
页码:899 / 904
页数:6
相关论文
共 23 条
[1]  
ALLSOP D, 1990, AM J PATHOL, V136, P255
[2]  
BONDAREFF W, 1990, AM J PATHOL, V137, P711
[3]  
CRAS P, 1990, AM J PATHOL, V137, P241
[4]   ALZ-50 ANTIBODY RECOGNIZES ALZHEIMER-RELATED NEURONAL CHANGES [J].
HYMAN, BT ;
VANHOESEN, GW ;
WOLOZIN, BL ;
DAVIES, P ;
KROMER, LJ ;
DAMASIO, AR .
ANNALS OF NEUROLOGY, 1988, 23 (04) :371-379
[5]   A4 AMYLOID PROTEIN IMMUNOREACTIVITY IS PRESENT IN ALZHEIMERS-DISEASE NEUROFIBRILLARY TANGLES [J].
HYMAN, BT ;
VANHOESEN, GW ;
BEYREUTHER, K ;
MASTERS, CL .
NEUROSCIENCE LETTERS, 1989, 101 (03) :352-355
[6]   ANTIBODIES TO PAIRED HELICAL FILAMENTS IN ALZHEIMERS-DISEASE DO NOT RECOGNIZE NORMAL BRAIN PROTEINS [J].
IHARA, Y ;
ABRAHAM, C ;
SELKOE, DJ .
NATURE, 1983, 304 (5928) :727-730
[7]   DIAGNOSIS OF ALZHEIMERS-DISEASE [J].
KHACHATURIAN, ZS .
ARCHIVES OF NEUROLOGY, 1985, 42 (11) :1097-1104
[8]   A68 - A MAJOR SUBUNIT OF PAIRED HELICAL FILAMENTS AND DERIVATIZED FORMS OF NORMAL-TAU [J].
LEE, VMY ;
BALIN, BJ ;
OTVOS, L ;
TROJANOWSKI, JQ .
SCIENCE, 1991, 251 (4994) :675-678
[9]   UBIQUITIN IS ASSOCIATED WITH ABNORMAL CYTOPLASMIC FILAMENTS CHARACTERISTIC OF NEURODEGENERATIVE DISEASES [J].
MANETTO, V ;
PERRY, G ;
TABATON, M ;
MULVIHILL, P ;
FRIED, VA ;
SMITH, HT ;
GAMBETTI, P ;
AUTILIOGAMBETTI, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4501-4505
[10]  
OKAMOTO K, 1982, CLIN NEUROL, V22, P840