Selectively enhanced contextual fear conditioning in mice lacking the transcriptional regulator CCAAT/enhancer binding protein δ

被引:130
作者
Sterneck, E
Paylor, R
Jackson-Lewis, V
Libbey, M
Przedborski, S
Tessarollo, L
Crawley, JN
Johnson, PF [1 ]
机构
[1] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Eukaryot Transcript Regulat Sect, Frederick, MD 21702 USA
[2] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Neural Dev Grp, Frederick, MD 21702 USA
[3] Columbia Univ, Dept Neurol, Neurol Res Movement Disorders Div, New York, NY 10032 USA
[4] NIMH, Sect Behav Neuropharmacol, Expt Therapeut Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.95.18.10908
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
CCAAT/enhancer binding protein delta (C/EBP delta) is a transcriptional regulator implicated in the hepatic acute phase response and in adipogenic and myeloid cell differentiation. We found that C/EBP delta is widely expressed in the peripheral and central nervous systems, including neurons of the hippocampal formation, indicating a role in neural functions. To examine the role of C/EBP delta in vivo, we generated mice with a targeted deletion of the C/EBP delta gene. This mutation does not interfere with normal embryonic and postnatal development. Performance in a battery of behavioral tests indicates that basic neurological functions are normal. Furthermore, performance in a Morris water maze task suggests that C/EBP delta mutant mice have normal spatial learning. However, in the contextual and auditory-cue-conditioned fear task, C/EBP delta null mice displayed significantly more conditioned freezing to the test context than did wild-type controls, but equivalent conditioning to the auditory cue, These data demonstrate a selectively enhanced contextual fear response in mice carrying a targeted genomic mutation and implicate C/EBP delta in the regulation of a specific type of learning and memory.
引用
收藏
页码:10908 / 10913
页数:6
相关论文
共 50 条
[1]   Genetic demonstration of a role for PKA in the late phase of LTP and in hippocampus-based long-term memory [J].
Abel, T ;
Nguyen, PV ;
Barad, M ;
Deuel, TAS ;
Kandel, ER .
CELL, 1997, 88 (05) :615-626
[2]   Memory suppressor genes: Inhibitory constraints on the storage of long-term memory [J].
Abel, T ;
Martin, KC ;
Bartsch, D ;
Kandel, ER .
SCIENCE, 1998, 279 (5349) :338-341
[3]   C/EBP IS AN IMMEDIATE-EARLY GENE REQUIRED FOR THE CONSOLIDATION OF LONG-TERM FACILITATION IN APLYSIA [J].
ALBERINI, CM ;
GHIRARDI, M ;
METZ, R ;
KANDEL, ER .
CELL, 1994, 76 (06) :1099-1114
[4]   APLYSIA CREB2 REPRESSES LONG-TERM FACILITATION - RELIEF OF REPRESSION CONVERTS TRANSIENT FACILITATION INTO LONG-TERM FUNCTIONAL AND STRUCTURAL-CHANGE [J].
BARTSCH, D ;
GHIRARDI, M ;
SKEHEL, PA ;
KARL, KA ;
HERDER, SP ;
CHEN, M ;
BAILEY, CH ;
KANDEL, ER .
CELL, 1995, 83 (06) :979-992
[5]   DEFICIENT LONG-TERM-MEMORY IN MICE WITH A TARGETED MUTATION OF THE CAMP-RESPONSIVE ELEMENT-BINDING PROTEIN [J].
BOURTCHULADZE, R ;
FRENGUELLI, B ;
BLENDY, J ;
CIOFFI, D ;
SCHUTZ, G ;
SILVA, AJ .
CELL, 1994, 79 (01) :59-68
[6]   DEFECT IN CYCLIC-AMP PHOSPHODIESTERASE DUE TO THE DUNCE MUTATION OF LEARNING IN DROSOPHILA-MELANOGASTER [J].
BYERS, D ;
DAVIS, RL ;
KIGER, JA .
NATURE, 1981, 289 (5793) :79-81
[7]   Interleukin-6-specific activation of the C/EBPδ gene in hepatocytes is mediated by Stat3 and Sp1 [J].
Cantwell, CA ;
Sterneck, E ;
Johnson, PF .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :2108-2117
[8]  
Cardinaux JR, 1996, J NEUROSCI, V16, P919
[9]   Molecular genetic analysis of synaptic plasticity, activity-dependent neural development, learning, and memory in the mammalian brain [J].
Chen, C ;
Tonegawa, S .
ANNUAL REVIEW OF NEUROSCIENCE, 1997, 20 :157-184
[10]   PRELIMINARY-REPORT OF A SIMPLE ANIMAL BEHAVIOR MODEL FOR THE ANXIOLYTIC EFFECTS OF BENZODIAZEPINES [J].
CRAWLEY, J ;
GOODWIN, FK .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1980, 13 (02) :167-170