BETA-AMYLOID PRECURSOR PROTEIN GENE IS DIFFERENTIALLY EXPRESSED IN AXOTOMIZED SENSORY AND MOTOR SYSTEMS

被引:65
作者
SCOTT, JN
PARHAD, IM
CLARK, AW
机构
[1] UNIV CALGARY, HLTH SCI CTR,DEPT PATHOL,ROOM 2027, 3330 HOSP DR NW, CALGARY T2N 4N1, ALBERTA, CANADA
[2] UNIV CALGARY, DEPT CLIN NEUROSCI, CALGARY T2N 1N4, ALBERTA, CANADA
来源
MOLECULAR BRAIN RESEARCH | 1991年 / 10卷 / 04期
关键词
BETA-AMYLOID PRECURSOR PROTEIN; AXOTOMY; REGENERATION; SCIATIC NERVE; GENE EXPRESSION; ANTERIOR HORN CELL; DORSAL ROOT GANGLION; ALZHEIMERS DISEASE;
D O I
10.1016/0169-328X(91)90090-K
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The beta-amyloid precursor protein (APP) is involved in the degenerative and regenerative neural changes associated with aging and Alzheimer's disease. We studied the regulation of APP gene expression in a paradigm of degeneration and regeneration, the axotomized rat sciatic system. The sciatic nerves of rats were crushed and at intervals between 4 and 60 days, the affected dorsal root ganglia and spinal cord segments were processed for Northern analysis and in situ hybridization to evaluate various APP mRNA species. After nerve crush, dorsal root ganglia APP mRNA levels are increased for both APP695 (695 amino acids) and APP(KPI) (Kunitz protease inhibitor). Following reinnervation, APP695 returns to baseline but APP(KPI) remains elevated. In spinal cord there is a decrease of APP695, which returns to baseline following reinnervation. If regeneratin is prevented, the initial phase of post-axotomy response for all APP forms persists for at least 60 days in both dorsal root ganglia and spinal cord. In situ hybridization confirms that the changes are referable to neurons. These findings indicate that neuron-target interactions are important in APP gene regulation; that the APP695 and APP(KPI) transcripts are differentially regulated following neuronal injury; and that different neuronal populations regulate APP expression in a cell-type specific manner.
引用
收藏
页码:315 / 325
页数:11
相关论文
共 57 条
[1]   TRANSPORT OF ENDOGENOUS NERVE GROWTH-FACTOR IN THE PROXIMAL STUMP OF SECTIONED NERVES [J].
ABRAHAMSON, IK ;
BRIDGES, D ;
RUSH, RA .
JOURNAL OF NEUROCYTOLOGY, 1987, 16 (03) :417-422
[3]   PRIMARY STRUCTURE AND TRANSCRIPTIONAL REGULATION OF GAP-43, A PROTEIN ASSOCIATED WITH NERVE GROWTH [J].
BASI, GS ;
JACOBSON, RD ;
VIRAG, I ;
SCHILLING, J ;
SKENE, JHP .
CELL, 1987, 49 (06) :785-791
[4]   AXONAL ATROPHY FROM PERMANENT PERIPHERAL AXOTOMY IN ADULT CAT [J].
CARLSON, J ;
LAIS, AC ;
DYCK, PJ .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1979, 38 (06) :579-585
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   ALTERED EXPRESSION OF GENES FOR AMYLOID AND CYTOSKELETAL PROTEINS IN ALZHEIMER CORTEX [J].
CLARK, AW ;
KREKOSKI, CA ;
PARHAD, IM ;
LISTON, D ;
JULIEN, JP ;
HOAR, DI .
ANNALS OF NEUROLOGY, 1989, 25 (04) :331-339
[7]   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
[8]   MULTIPLE RANGE AND MULTIPLE F TESTS [J].
DUNCAN, DB .
BIOMETRICS, 1955, 11 (01) :1-42
[9]  
ENFORS P, 1989, NEURON, V2, P1605
[10]   CLEAVAGE OF AMYLOID-BETA PEPTIDE DURING CONSTITUTIVE PROCESSING OF ITS PRECURSOR [J].
ESCH, FS ;
KEIM, PS ;
BEATTIE, EC ;
BLACHER, RW ;
CULWELL, AR ;
OLTERSDORF, T ;
MCCLURE, D ;
WARD, PJ .
SCIENCE, 1990, 248 (4959) :1122-1124