ISOFORM-SPECIFIC INTERACTIONS OF APOLIPOPROTEIN-E WITH THE MICROTUBULE-ASSOCIATED PROTEIN MAP2C - IMPLICATIONS FOR ALZHEIMERS-DISEASE

被引:75
作者
HUANG, DY
GOEDERT, M
JAKES, R
WEISGRABER, KH
GARNER, CC
SAUNDERS, AM
PERICAKVANCE, MA
SCHMECHEL, DE
ROSES, AD
STRITTMATTER, WJ
机构
[1] DUKE UNIV,MED CTR,DIV NEUROL,DEPT MED NEUROL,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,JOSEPH & KATHLEEN BRYAN ALZHEIMERS DIS RES CTR,DEPT NEUROBIOL,DURHAM,NC 27710
[3] MRC,MOLEC BIOL LAB,CAMBRIDGE,ENGLAND
[4] UNIV CALIF SAN FRANCISCO,GLADSTONE INST CARDIOVASC DIS,CARDIOVASC RES INST,DEPT PATHOL,SAN FRANCISCO,CA 94141
[5] UNIV ALABAMA,MED CTR,DEPT NEUROBIOL,BIRMINGHAM,AL 35294
关键词
APOLIPOPROTEIN E; MICROTUBULE-ASSOCIATED PROTEIN; MAP2C; ALZHEIMERS DISEASE;
D O I
10.1016/0304-3940(94)90204-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The apolipoprotein E type 4 allele is a susceptibility gene for late-onset Alzheimer's disease. Apolipoprotein E is found in neurons, some of which contain paired helical filaments made of the microtubule-associated protein tau. Previous studies have demonstrated that the apoE3 isoform, but not the apoE4 isoform, binds tau with high avidity. Because the microtubule-associated protein MAP2c also effects microtubule assembly and stability, we examined interactions between apoE isoforms and MAP2c. Similar to the tau-binding results, apoE3, but not apoE4, bound MAP2c. Binding was detectable down to 10(-9) M MAP2c and 10(-8) M apoE3. Isoform-specific interactions of apoE with the microtubule-associated proteins MAP2c and tau might affect intracellular maintenance of microtubules and could contribute to a time-dependent pathogenesis of Alzheimer's disease.
引用
收藏
页码:55 / 58
页数:4
相关论文
共 24 条
[1]   ABNORMAL TAU-PHOSPHORYLATION AT SER(396) IN ALZHEIMERS-DISEASE RECAPITULATES DEVELOPMENT AND CONTRIBUTES TO REDUCED MICROTUBULE-BINDING [J].
BRAMBLETT, GT ;
GOEDERT, M ;
JAKES, R ;
MERRICK, SE ;
TROJANOWSKI, JQ ;
LEE, VMY .
NEURON, 1993, 10 (06) :1089-1099
[2]  
Bulinski Jeannette Chloe, 1994, V13, P167
[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]  
CORDER EH, IN PRESS NATURE GEN
[5]   ASSEMBLY OF ALZHEIMER-LIKE FILAMENTS FROM FULL-LENGTH TAU-PROTEIN [J].
CROWTHER, RA ;
OLESEN, OF ;
SMITH, MJ ;
JAKES, R ;
GOEDERT, M .
FEBS LETTERS, 1994, 337 (02) :135-138
[6]   DIFFERENT FORMS OF MICROTUBULE-ASSOCIATED PROTEIN-2 ARE ENCODED BY SEPARATE MESSENGER-RNA TRANSCRIPTS [J].
GARNER, CC ;
MATUS, A .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :779-783
[7]   MOLECULAR CHARACTERIZATION OF MICROTUBULE-ASSOCIATED PROTEINS-TAU AND MAP2 [J].
GOEDERT, M ;
CROWTHER, RA ;
GARNER, CC .
TRENDS IN NEUROSCIENCES, 1991, 14 (05) :193-199
[8]   EXPRESSION OF SEPARATE ISOFORMS OF HUMAN TAU-PROTEIN - CORRELATION WITH THE TAU-PATTERN IN BRAIN AND EFFECTS ON TUBULIN POLYMERIZATION [J].
GOEDERT, M ;
JAKES, R .
EMBO JOURNAL, 1990, 9 (13) :4225-4230
[9]   MULTIPLE ISOFORMS OF HUMAN MICROTUBULE-ASSOCIATED PROTEIN-TAU - SEQUENCES AND LOCALIZATION IN NEUROFIBRILLARY TANGLES OF ALZHEIMERS-DISEASE [J].
GOEDERT, M ;
SPILLANTINI, MG ;
JAKES, R ;
RUTHERFORD, D ;
CROWTHER, RA .
NEURON, 1989, 3 (04) :519-526
[10]  
HAN SH, IN PRESS EXP NEUROL