Comparison of neuroplastin and synaptic marker protein expression in acute and cultured organotypic hippocampal slices from rat

被引:20
作者
Buckby, LE [1 ]
Mummery, R [1 ]
Crompton, MR [1 ]
Beesley, PW [1 ]
Empson, RM [1 ]
机构
[1] Univ London Royal Holloway & Bedford New Coll, Sch Biol Sci, Egham TW20 0EX, Surrey, England
来源
DEVELOPMENTAL BRAIN RESEARCH | 2004年 / 150卷 / 01期
基金
英国生物技术与生命科学研究理事会;
关键词
development and regeneration; genesis of neurotics and glia; organotypic; hippocampus; synaptogenesis; neuroplastin; PSD95; development;
D O I
10.1016/j.devbrainres.2004.01.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organotypic hippocampal slice cultures can be used to Study hippocampal biochemistry and physiology over a chronic period on the days to weeks timescale. In order to validate the organotypic hippocampal slice culture for our ongoing studies of synaptic function, we have compared, using Western blotting, the levels of a number of synaptic proteins from in vitro organotypic hippocampal slice cultures with those from in vivo hippocampal slices prepared from age-matched controls. We chose to follow the developmental expression of the neuroplastin (np) family of immunoglobulin related cell adhesion molecules (CAMs), np65, a brain specific isoform highly expressed in hippocampal neurones and np55 a more widely expressed isoform and two synaptic marker proteins, synaptophysin, a pre-synaptic marker and postsynaptic density protein-95, PSD95, a post-synaptic marker. All showed increasing expression over the developmental time period, both in vivo and in vitro. The level of both neuroplastins was also consistent between the in vivo and in vitro preparations, whereas the level of PSD95 was markedly increased in the organotypic hippocampal slice Cultures while the level of synaptophysin was slightly decreased. Whilst these findings may indicate some differences in the composition and organisation of synapses, the developmental expression profiles of these synaptic proteins within organotypic hippocampal Slice Cultures suggests they are a valid model for the study of synapse function and development in vitro. (C) 2004 Elsevier B.V. All rights reserved.
引用
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页码:1 / 7
页数:7
相关论文
共 32 条
[1]  
Beesley PW, 2000, EUR J NEUROSCI, V12, P276
[2]   Making memories stick: cell-adhesion molecules in synaptic plasticity [J].
Benson, DL ;
Schnapp, LM ;
Shapiro, L ;
Huntley, GW .
TRENDS IN CELL BIOLOGY, 2000, 10 (11) :473-482
[3]  
CALAKOS N, 1994, J BIOL CHEM, V269, P24534
[4]   Pathophysiological implications of the structural organization of the excitatory synapse [J].
Cattabeni, F ;
Gardoni, F ;
Di Luca, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 375 (1-3) :339-347
[5]   Development of rat CA1 neurones in acute versus organotypic slices:: role of experience in synaptic morphology and activity [J].
De Simoni, A ;
Griesinger, CB ;
Edwards, FA .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 550 (01) :135-147
[6]   The tubulin fraternity: alpha to eta [J].
Dutcher, SK .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (01) :49-54
[7]   Ca2+ entry through L-type Ca2+ channels helps terminate epileptiform activity by activation of a Ca2+ dependent afterhyperpolarisation in hippocampal CA3 [J].
Empson, RM ;
Jefferys, JGR .
NEUROSCIENCE, 2001, 102 (02) :297-306
[8]   Organotypic slice cultures: a technique has come of age [J].
Gahwiler, BH ;
Capogna, M ;
Debanne, D ;
McKinney, RA ;
Thompson, SM .
TRENDS IN NEUROSCIENCES, 1997, 20 (10) :471-477
[9]   Molecular mechanisms of CNS synaptogenesis [J].
Garner, CC ;
Zhai, RG ;
Gundelfinger, ED ;
Ziv, NE .
TRENDS IN NEUROSCIENCES, 2002, 25 (05) :243-250
[10]   EXPRESSION OF 2 SYNAPSE-ENRICHED GLYCOPROTEINS, GP65 AND GP55, DURING RAT-BRAIN DEVELOPMENT [J].
HILL, I ;
WILLMOTT, T ;
SKITSA, I ;
SELKIRK, C ;
MURPHY, S ;
GORDONWEEKS, P ;
BEESLEY, P .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1989, 17 (04) :770-771