Characterization of the AD7C-NTP cDNA expression in Alzheimer's disease and measurement of a 41-kD protein in cerebrospinal fluid

被引:99
作者
de la Monte, SM
Ghanbari, K
Frey, WH
Beheshti, I
Averback, P
Hauser, SL
Ghanbari, HA
Wands, JR
机构
[1] Massachusetts Gen Hosp, MGH E Canc Ctr, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, MGH Alzheimers Dis Res Ctr, Charlestown, MA 02129 USA
[3] Massachusetts Gen Hosp, Dept Pathol, Charlestown, MA 02129 USA
[4] Massachusetts Gen Hosp, Dept Med, Charlestown, MA 02129 USA
[5] Harvard Univ, Sch Med, Boston, MA 02114 USA
[6] Nymox Corp, Rockville, MD 20895 USA
[7] Ramsey Alzheimers Treatment & Res Ctr, St Paul, MN 55101 USA
[8] Univ Calif San Francisco, Med Ctr, San Francisco, CA 94143 USA
关键词
AD7c-NTP; Alzheimer's Disease; cerebrospinal fluid; enzyme immunoassay; neurodegeneration; Alu sequence;
D O I
10.1172/JCI119864
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We have isolated a novel Alu sequence-containing cDNA, designated AD7c-NTP, that is expressed in neurons, and overexpressed in brains with Alzheimer's disease (AD). The 1,442-nucleotide AD7c-NTP cDNA encodes an similar to 41-kD protein, Expression of AD7c-NTP was confirmed by nucleic acid sequencing of reverse transcriptase PCR products isolated from brain, AD7c-NTP cDNA probes hybridized with 1.4 kB mRNA transcripts by Northern blot analysis, and monoclonal antibodies generated with the recombinant protein were immunoreactive with similar to 41-45-kD and similar to 18-21-kD molecules by Western blot analysis. In situ hybridization and immunostaining studies localized AD7c-NTP gene expression in neurons, Using a quantitative enzyme-linked sandwich immunoassay (Ghanbari, K., I. Beheshti, and H. Ghanbari, manuscript submitted for publication) constructed with antibodies to the recombinant protein, AD7c-NTP levels were measured under code in 323 clinical and postmortem cerebrospinal fluid (CSF) samples from AD, age-matched control, Parkinson's disease, and neurological disease control patients. The molecular mass of the AD7c-NTP detected in CSF was similar to 41 kD, In postmortem CSF, the mean concentration of AD7c-NTP in cases of definite AD (9.2+/-8.2 ng/ml) was higher than in the aged control group (1.6+/-0.9; P < 0.0001), In CSF samples from individuals with early possible or probable AD, the mean concentration of AD7c-NTP (4.6+/-3.4) was also elevated relative to the levels in CSF from age-matched (1.2+/-0.7) and neurological disease (1.0+/-0.9) controls, and ambulatory patients with Parkinson's disease (1.8+/-1.1) (all P < 0.001), CSF levels of AD7c-NTP were correlated with Blessed dementia scale scores (r = 0.66; P = 0.0001) rather than age (r = -0.06; P > 0.1), In vitro studies demonstrated that overexpression of AD7c-NTP in transfected neuronal cells promotes neuritic sprouting and cell death, the two principal neuroanatomical lesions correlated with dementia in AD. The results suggest that abnormal AD7c-NTP expression is associated with AD neurodegeneration, and during the early stages of disease, CSF levels correlate with the severity of dementia.
引用
收藏
页码:3093 / 3104
页数:12
相关论文
共 51 条
[1]   The functional significance of brain metallothioneins [J].
Aschner, M .
FASEB JOURNAL, 1996, 10 (10) :1129-1136
[2]  
Ausubel FM., 1997, CURRENT PROTOCOLS MO, p13.1, DOI DOI 10.1.4
[3]  
BARINAGA M, 1995, SCIENCE, V269, P973
[4]   SENSITIVE AND SPECIFIC ASSAY FOR HUMAN CHORIONIC-GONADOTROPIN (HCG) BASED ON ANTIPEPTIDE AND ANTI-HCG MONOCLONAL-ANTIBODIES - CONSTRUCTION AND CLINICAL IMPLICATIONS [J].
BELLET, DH ;
OZTURK, M ;
BIDART, JM ;
BOHUON, CJ ;
WANDS, JR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (06) :1319-1327
[5]  
BIEDLER JL, 1973, CANCER RES, V33, P2643
[6]   GENE-EXPRESSION AND CELLULAR CONTENT OF CATHEPSIN-D IN ALZHEIMERS-DISEASE BRAIN - EVIDENCE FOR EARLY UP-REGULATION OF THE ENDOSOMAL LYSOSOMAL SYSTEM [J].
CATALDO, AM ;
BARNETT, JL ;
BERMAN, SA ;
LI, JH ;
QUARLESS, S ;
BURSZTAJN, S ;
LIPPA, C ;
NIXON, RA .
NEURON, 1995, 14 (03) :671-680
[7]   IMPAIRMENT IN MITOCHONDRIAL CYTOCHROME-OXIDASE GENE-EXPRESSION IN ALZHEIMER-DISEASE [J].
CHANDRASEKARAN, K ;
GIORDANO, T ;
BRADY, DR ;
STOLL, J ;
MARTIN, LJ ;
RAPOPORT, SI .
MOLECULAR BRAIN RESEARCH, 1994, 24 (1-4) :336-340
[8]   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
[9]  
DALLMAN MJ, 1991, PCR PRACTICAL APPROA, P215
[10]   SYNAPSE LOSS IN FRONTAL-CORTEX BIOPSIES IN ALZHEIMERS-DISEASE - CORRELATION WITH COGNITIVE SEVERITY [J].
DEKOSKY, ST ;
SCHEFF, SW .
ANNALS OF NEUROLOGY, 1990, 27 (05) :457-464