TRANSTHYRETIN SEQUESTERS AMYLOID-BETA PROTEIN AND PREVENTS AMYLOID FORMATION

被引:350
作者
SCHWARZMAN, AL
GREGORI, L
VITEK, MP
LYUBSKI, S
STRITTMATTER, WJ
ENGHILDE, JJ
BHASIN, R
SILVERMAN, J
WEISGRABER, KH
COYLE, PK
ZAGORSKI, MG
TALAFOUS, J
EISENBERG, M
SAUNDERS, AM
ROSES, AD
GOLDGABER, D
机构
[1] SUNY STONY BROOK, SCH MED, DEPT PSYCHIAT, STONY BROOK, NY 11794 USA
[2] SUNY STONY BROOK, SCH MED, DEPT PATHOL, STONY BROOK, NY 11794 USA
[3] SUNY STONY BROOK, SCH MED, DEPT NEUROL, STONY BROOK, NY 11794 USA
[4] SUNY STONY BROOK, SCH MED, DEPT PHARMACOL, STONY BROOK, NY 11794 USA
[5] PICOWER INST MED RES, MANHASSET, NY 11030 USA
[6] DUKE UNIV, MED CTR, JOSEPH & KATHLEEN BRYAN ALZHEIMERS RES CTR, DEPT MED NEUROL, DURHAM, NC 27710 USA
[7] DUKE UNIV, MED CTR, DEPT PATHOL, DURHAM, NC 27710 USA
[8] UNIV CALIF SAN FRANCISCO, J DAVID GLADSTONE INST CARDIOVASC DIS, DEPT PATHOL, SAN FRANCISCO, CA 94110 USA
[9] CASE WESTERN RESERVE UNIV, DEPT CHEM, CLEVELAND, OH 44106 USA
关键词
SEQUESTRATION;
D O I
10.1073/pnas.91.18.8368
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
The cardinal pathological features of Alzheimer disease are depositions of aggregated amyloid beta protein (A beta) in the brain and cerebrovasculature. However, the A beta is found in a soluble form in cerebrospinal fluid in healthy individuals and patients with Alzheimer disease. We postulate that sequestration of A beta precludes amyloid formation. Failure to sequester A beta in Alzheimer disease may result in amyloidosis. When we added A beta to cerebrospinal fluid of patients and controls it was rapidly sequestered into stable complexes with transthyretin. Complexes with apolipoprotein E, which has been shown to bind A beta in vitro, were not observed in cerebrospinal fluid. Additional in vitro studies showed that both purified transthyretin and apolipoprotein E prevent amyloid formation.
引用
收藏
页码:8368 / 8372
页数:5
相关论文
共 36 条
  • [1] BETA-AMYLOID STIMULATES GLIAL-CELLS INVITRO TO PRODUCE GROWTH-FACTORS THAT ACCUMULATE IN SENILE PLAQUES IN ALZHEIMERS-DISEASE
    ARAUJO, DM
    COTMAN, CW
    [J]. BRAIN RESEARCH, 1992, 569 (01) : 141 - 145
  • [2] VITAMIN-E PROTECTS NERVE-CELLS FROM AMYLOID BETA-PROTEIN TOXICITY
    BEHL, C
    DAVIS, J
    COLE, GM
    SCHUBERT, D
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) : 944 - 950
  • [3] BENSON MD, 1989, METABOLIC BASIS INHE, V2, P2439
  • [4] STRUCTURE OF PRE-ALBUMIN - SECONDARY, TERTIARY AND QUATERNARY INTERACTIONS DETERMINED BY FOURIER REFINEMENT AT 1.8-A
    BLAKE, CCF
    GEISOW, MJ
    OATLEY, SJ
    RERAT, B
    RERAT, C
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1978, 121 (03) : 339 - 356
  • [5] BURDICK D, 1992, J BIOL CHEM, V267, P546
  • [6] CASTANO EM, 1988, LAB INVEST, V58, P122
  • [7] INVITRO FORMATION OF AMYLOID FIBRILS FROM 2 SYNTHETIC PEPTIDES OF DIFFERENT LENGTHS HOMOLOGOUS TO ALZHEIMERS-DISEASE BETA-PROTEIN
    CASTANO, EM
    GHISO, J
    PRELLI, F
    GOREVIC, PD
    MIGHELI, A
    FRANGIONE, B
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 141 (02) : 782 - 789
  • [8] SP-40,40 IS A CONSTITUENT OF ALZHEIMERS AMYLOID
    CHOIMIURA, NH
    IHARA, Y
    FUKUCHI, K
    TAKEDA, M
    NAKANO, Y
    TOBE, T
    TOMITA, M
    [J]. ACTA NEUROPATHOLOGICA, 1992, 83 (03) : 260 - 264
  • [9] INSITU HYBRIDIZATION OF NUCLEUS BASALIS NEURONS SHOWS INCREASED BETA-AMYLOID MESSENGER-RNA IN ALZHEIMER-DISEASE
    COHEN, ML
    GOLDE, TE
    USIAK, MF
    YOUNKIN, LH
    YOUNKIN, SG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (04) : 1227 - 1231
  • [10] GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES
    CORDER, EH
    SAUNDERS, AM
    STRITTMATTER, WJ
    SCHMECHEL, DE
    GASKELL, PC
    SMALL, GW
    ROSES, AD
    HAINES, JL
    PERICAKVANCE, MA
    [J]. SCIENCE, 1993, 261 (5123) : 921 - 923