Progressive decline in avoidance learning paralleled by inflammatory neurodegeneration in transgenic mice expressing interleukin 6 in the brain

被引:332
作者
Heyser, CJ
Masliah, E
Samimi, A
Campbell, IL
Gold, LH
机构
[1] Scripps Res Inst, DEPT NEUROPHARMACOL, LA JOLLA, CA 92037 USA
[2] UNIV CALIF SAN DIEGO, SCH MED, DEPT NEUROSCI, LA JOLLA, CA 92093 USA
[3] UNIV CALIF SAN DIEGO, SCH MED, DEPT PATHOL, LA JOLLA, CA 92093 USA
关键词
dementia; neuropathology; microgliosis; cytokine; calbindin;
D O I
10.1073/pnas.94.4.1500
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
Inflammation with expression of interleukin 6 (IL-6) in the brain occurs in many neurodegentrative disorders, To better understand the role of IL-6 in such disorders, we examined performance in a learning task in conjunction with molecular and cellular neuropathology in transgenic mice that express IL-6 chronically from astrocytes in the brain, Transgenic mice exhibited dose- and age-related deficits in avoidance learning that closely corresponded with specific progressive neuropathological changes. These results establish a link between the central nervous system expression of IL-6, inflammatory neurodegeneration, and a learning impairment in transgenic mice, They suggest a critical role for a proinflammatory cytokine in the cognitive deficits and associated neuroinflammatory changes that have been documented in neurodegenerative diseases such as Alzheimer disease and AIDS.
引用
收藏
页码:1500 / 1505
页数:6
相关论文
共 43 条
[1]   BIOLOGY OF MULTIFUNCTIONAL CYTOKINES - IL-6 AND RELATED MOLECULES (IL-1 AND TNF) [J].
AKIRA, S ;
HIRANO, T ;
TAGA, T ;
KISHIMOTO, T .
FASEB JOURNAL, 1990, 4 (11) :2860-2867
[2]  
BACH ME, 1995, CELL, V81, P901
[3]   CYTOTOXICITY OF MICROGLIA [J].
BANATI, RB ;
GEHRMANN, J ;
SCHUBERT, P ;
KREUTZBERG, GW .
GLIA, 1993, 7 (01) :111-118
[4]  
Barnum SR, 1996, GLIA, V18, P107, DOI 10.1002/(SICI)1098-1136(199610)18:2<107::AID-GLIA3>3.0.CO
[5]  
2-Y
[6]   INTERLEUKIN-6 AND ALPHA-2-MACROGLOBULIN INDICATE AN ACUTE-PHASE STATE IN ALZHEIMERS-DISEASE CORTICES [J].
BAUER, J ;
STRAUSS, S ;
SCHREITERGASSER, U ;
GANTER, U ;
SCHLEGEL, P ;
WITT, I ;
YOLK, B ;
BERGER, M .
FEBS LETTERS, 1991, 285 (01) :111-114
[7]   EVOLUTION OF NEUROPATHOLOGIC ABNORMALITIES ASSOCIATED WITH BLOOD-BRAIN-BARRIER BREAKDOWN IN TRANSGENIC MICE EXPRESSING INTERLEUKIN-6 IN ASTROCYTES [J].
BRETT, FM ;
MIZISIN, AP ;
POWELL, HC ;
CAMPBELL, IL .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (06) :766-775
[8]   NEUROLOGIC DISEASE INDUCED IN TRANSGENIC MICE BY CEREBRAL OVEREXPRESSION OF INTERLEUKIN-6 [J].
CAMPBELL, IL ;
ABRAHAM, CR ;
MASLIAH, E ;
KEMPER, P ;
INGLIS, JD ;
OLDSTONE, MBA ;
MUCKE, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) :10061-10065
[9]   PARVALBUMIN IN MOST GAMMA-AMINOBUTYRIC-ACID CONTAINING NEURONS OF THE RAT CEREBRAL-CORTEX [J].
CELIO, MR .
SCIENCE, 1986, 231 (4741) :995-997
[10]   SYNAPTIC LOSS IN COGNITIVELY IMPAIRED AGED RATS IS AMELIORATED BY CHRONIC HUMAN NERVE GROWTH-FACTOR INFUSION [J].
CHEN, KS ;
MASLIAH, E ;
MALLORY, M ;
GAGE, FH .
NEUROSCIENCE, 1995, 68 (01) :19-27