LONG-TERM HIPPOCAMPAL SLICES - A MODEL SYSTEM FOR INVESTIGATING SYNAPTIC MECHANISMS AND PATHOLOGICAL PROCESSES

被引:127
作者
BAHR, BA
机构
[1] Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine
关键词
AGING; ALZHEIMERS DISEASE; EXCITOTOXICITY; LYSOSOMAL DYSFUNCTION; ORGANOTYPIC CULTURES; SYNAPTIC PLASTICITY;
D O I
10.1002/jnr.490420303
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Organotypic cultures provide a unique strategy with which to examine many aspects of brain physiology and pathology, Long-term slice cultures from the hippocampus, a region involved in memory encoding and one that exhibits early degeneration in Alzheimer's disease and ischemia, are particularly valuable in this regard due to their expression of synaptic plasticity mechanisms (e.g., long-term potentiation) and responsiveness to pathological insults (e.g., excitotoxicity), Long-term slices can be prepared from hippocampi at the second or third postnatal week of development and thus incorporate a number of relatively mature features; further signs of maturation and the preservation of adult-like characteristics occur over succeeding weeks, The stability of the cultured slice renders it an appropriate model for studying 1) prolonged regulation/stabilization events linked to synaptogenesis and certain forms of plasticity, 2) temporal patterns of cellular atrophy associated with pathogenic conditions such as ischemia and epilepsia, and 3) slow processes associated with aging and age-related pathologies. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:294 / 305
页数:12
相关论文
共 98 条
[1]   NEUROTOXICITY OF BETA-AMYLOID PROTEIN - CYTOCHEMICAL CHANGES AND APOPTOTIC CELL-DEATH INVESTIGATED IN ORGANOTYPIC CULTURES [J].
ALLEN, YS ;
DEVANATHAN, PH ;
OWEN, GP .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1995, 22 (05) :370-371
[2]   A CENTRALLY ACTIVE-DRUG THAT MODULATES AMPA RECEPTOR GATED CURRENTS [J].
ARAI, A ;
KESSLER, M ;
XIAO, P ;
AMBROSINGERSON, J ;
ROGERS, G ;
LYNCH, G .
BRAIN RESEARCH, 1994, 638 (1-2) :343-346
[3]  
Bahr B. A., 1994, Molecular Biology of the Cell, V5, p468A
[4]   MOUSE TELENCEPHALON EXHIBITS AN AGE-RELATED DECREASE IN GLUTAMATE (AMPA) RECEPTORS BUT NO CHANGE IN NERVE-TERMINAL MARKERS [J].
BAHR, BA ;
GODSHALL, AC ;
HALL, RA ;
LYNCH, G .
BRAIN RESEARCH, 1992, 589 (02) :320-326
[5]   RAPID AND STABLE GENE-EXPRESSION IN HIPPOCAMPAL SLICE CULTURES FROM A DEFECTIVE HSV-1 VECTOR [J].
BAHR, BA ;
NEVE, RL ;
SHARP, J ;
GELLER, AI ;
LYNCH, G .
MOLECULAR BRAIN RESEARCH, 1994, 26 (1-2) :277-285
[6]   PURIFICATION OF AN ARG-GLY-ASP SELECTIVE MATRIX RECEPTOR FROM BRAIN SYNAPTIC PLASMA-MEMBRANES [J].
BAHR, BA ;
LYNCH, G .
BIOCHEMICAL JOURNAL, 1992, 281 :137-142
[7]  
BAHR BA, 1995, J PHARMACOL EXP THER, V273, P902
[8]   CHANGES IN THE CONCENTRATIONS OF TAU AND OTHER STRUCTURAL PROTEINS IN THE BRAINS OF AGED MICE [J].
BAHR, BA ;
LAM, N ;
LYNCH, G .
NEUROSCIENCE LETTERS, 1994, 175 (1-2) :49-52
[9]   INDUCTION OF BETA-AMYLOID-CONTAINING POLYPEPTIDES IN HIPPOCAMPUS - EVIDENCE FOR A CONCOMITANT LOSS OF SYNAPTIC PROTEINS AND INTERACTIONS WITH AN EXCITOTOXIN [J].
BAHR, BA ;
ABAI, B ;
GALL, CM ;
VANDERKLISH, PW ;
HOFFMAN, KB ;
LYNCH, G .
EXPERIMENTAL NEUROLOGY, 1994, 129 (01) :81-94
[10]   SPECTRIN BREAKDOWN PRODUCTS INCREASE WITH AGE IN TELENCEPHALON OF MOUSE-BRAIN [J].
BAHR, BA ;
VANDERKLISH, PW ;
HA, LT ;
TIN, MT ;
LYNCH, G .
NEUROSCIENCE LETTERS, 1991, 131 (02) :237-240