Molecular heterogeneity along the dorsal-ventral axis of the murine hippocampal CA1 field: A microarray analysis of gene expression

被引:63
作者
Leonardo, ED [1 ]
Richardson-Jones, JW
Sibille, E
Kottman, A
Hen, R
机构
[1] Columbia Univ, Ctr Neurobiol & Behav, New York, NY 10027 USA
[2] Columbia Univ, Dept Psychiat, New York, NY 10032 USA
[3] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[4] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[5] Russ Berrie Med Sci Pavil, Columbia Genome Ctr, New York, NY 10032 USA
[6] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA
关键词
microarray; hippocampus; CA1; septotemporal; dorsal-ventral; neuroanatomy;
D O I
10.1016/j.neuroscience.2005.08.082
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
There has been increasing interest in functional heterogeneity along the septotemporal, dorsal-ventral (D-V) axis of the hippocampus. Although anatomical connectivity and lesion studies point to discrete roles for these sub-regions, the contribution of differential gene expression across this axis has not been systematically studied. Here we present findings from an Affymetrix microarray screen aimed at identifying genes in the CA1 region of the adult murine hippocampus that show significant differential expression along the D-V axis. Our results indicate that the vast majority of monitored genes (> 90%) had tissue expression levels that differed by less than 20% between regions, while less than 0.1% of genes had expression levels that varied more than three-fold by sub-region. Only 23 probes showed a CA1 dorsoventral signal intensity ratio greater than three: 18 enriched dorsally and five enriched ventrally. Probes with the greatest difference in expression levels represent a range of genes with known functions in patterning and signaling, as well as genes without known function. Selective screening with digoxigenin-labeled in situ hybridization confirms the existence of CA1 sub-regionalized expression, with some genes exhibiting a graded expression pattern across the D-V axis, and others restricted to a discrete region. Our findings demonstrate that there are gene expression differences across the D-V axis of the adult murine hippocampus within traditionally recognized cytoarchitecturally defined boundaries. Combined with the previously recognized differences in connectivity and results from lesion studies, our data further confirm the existence of functional heterogeneity along the D-V axis. (c) 2005 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 42 条
[1]   THE 3-DIMENSIONAL ORGANIZATION OF THE HIPPOCAMPAL-FORMATION - A REVIEW OF ANATOMICAL DATA [J].
AMARAL, DG ;
WITTER, MP .
NEUROSCIENCE, 1989, 31 (03) :571-591
[2]  
ANDERSEN P, 1971, EXP BRAIN RES, V13, P222
[3]  
[Anonymous], 2000, NEUROPSYCHOLOGY ANXI
[4]   Regional dissociations within the hippocampus - memory and anxiety [J].
Bannerman, DM ;
Rawlins, JNP ;
McHugh, SB ;
Deacon, RMJ ;
Yee, BK ;
Bast, T ;
Zhang, WN ;
Pothuizen, HHJ ;
Feldon, J .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2004, 28 (03) :273-283
[5]   Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia [J].
Bannerman, DM ;
Deacon, RMJ ;
Offen, S ;
Friswell, J ;
Grubb, M ;
Rawlins, JNP .
BEHAVIORAL NEUROSCIENCE, 2002, 116 (05) :884-901
[6]   Double dissociation of function within the hippocampus: A comparison of dorsal, ventral, and complete hippocampal cytotoxic lesions [J].
Bannerman, DM ;
Yee, BK ;
Good, MA ;
Heupel, MJ ;
Iversen, SD ;
Rawlins, JNP .
BEHAVIORAL NEUROSCIENCE, 1999, 113 (06) :1170-1188
[7]  
Burwell RD, 1998, J COMP NEUROL, V391, P293, DOI 10.1002/(SICI)1096-9861(19980216)391:3<293::AID-CNE2>3.0.CO
[8]  
2-X
[9]  
CAJAL SRY, 1952, HISTOLOGIE SYSTAEME
[10]   Functional differentiation along the anterior-posterior axis of the hippocampus in monkeys [J].
Colombo, M ;
Fernandez, T ;
Nakamura, K ;
Gross, CG .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 80 (02) :1002-1005