Changes in neuronal migration in neocortex of connexin43 null mutant mice

被引:87
作者
Fushiki, S
Velazquez, JLP
Zhang, L
Bechberger, JF
Carlen, PL
Naus, CCG [1 ]
机构
[1] Univ British Columbia, Fac Med, Dept Anat & Cell Biol, Vancouver, BC V6T 1Z3, Canada
[2] Kyoto Prefectural Univ Med, Dept Pathol & Appl Neurobiol, Res Inst Neurol Dis & Geriatr, Kyoto, Japan
[3] Toronto Western Res Inst, Toronto, ON, Canada
[4] Bloorview Epilepsy Program, Toronto, ON, Canada
关键词
connexin43; migration; neocortex; neuron; null mutation;
D O I
10.1093/jnen/62.3.304
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To identify a neural phenotype in connexin43 null mutant mice, electrophysiological properties, intercellular communication and neuronal migration were studied in the developing neocortex. In acute slice preparations from newborn mice, electrophysiological characteristics of cortical and hippocampal neurons were not significantly different between wild type and null mutant mice. However, gap junctional coupling as assessed by fluorescence recovery after photobleaching was significantly attenuated in neocortical brain slices of null mutant mice. To assess neuronal migration, dividing cells were labeled with bromodeoxyuridine (BrdU) on embryonic days 12, 14 and 16, respectively, corresponding to the period of cortical neurogenesis, and the neocortex examined 2 or 3 days after the labeling. BrdU-labeled cells were distributed in the neocortical wall with a significant change in the pattern in the neocortex of the null mutant, where labeled cells accumulated in the intermediate zone or in the inner part of the cortical plate. The result suggests a significant delay in neocortical neuronal migration in the connexin43 null mutants, and a possible role of connexin43 in this process through yet unidentified mechanisms.
引用
收藏
页码:304 / 314
页数:11
相关论文
共 45 条
  • [1] BARTSCH S, 1992, J NEUROSCI, V12, P736
  • [2] BEHAR TN, 1994, J NEUROSCI, V14, P29
  • [3] Bittman K, 1997, J NEUROSCI, V17, P7037
  • [4] Neuronal heterotopias in the developing cerebral cortex produced by neurotrophin-4
    Brunstrom, JE
    GraySwain, MR
    Osborne, PA
    Pearlman, AL
    [J]. NEURON, 1997, 18 (03) : 505 - 517
  • [5] ARCHITECTONIC MAP OF NEOCORTEX OF NORMAL MOUSE
    CAVINESS, VS
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 1975, 164 (02) : 247 - 263
  • [6] Cloning of a new gap junction gene (Cx36) highly expressed in mammalian brain neurons
    Condorelli, DF
    Parenti, R
    Spinella, F
    Trovato-Salinaro, A
    Belluardo, N
    Cardile, V
    Cicirata, F
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (03) : 1202 - 1208
  • [7] A PROTEIN RELATED TO EXTRACELLULAR-MATRIX PROTEINS DELETED IN THE MOUSE MUTANT REELER
    DARCANGELO, G
    MIAO, GG
    CHEN, SC
    SOARES, HD
    MORGAN, JI
    CURRAN, T
    [J]. NATURE, 1995, 374 (6524) : 719 - 723
  • [8] DIFFERENTIAL EXPRESSION OF 3 GAP JUNCTION PROTEINS IN DEVELOPING AND MATURE BRAIN-TISSUES
    DERMIETZEL, R
    TRAUB, O
    HWANG, TK
    BEYER, E
    BENNETT, MVL
    SPRAY, DC
    WILLECKE, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 10148 - 10152
  • [9] Connexin43 null mice reveal that astrocytes express multiple connexins
    Dermietzel, R
    Gao, Y
    Scemes, E
    Vieria, D
    Urban, M
    Kremer, M
    Bennett, MVL
    Spray, DC
    [J]. BRAIN RESEARCH REVIEWS, 2000, 32 (01) : 45 - 56
  • [10] Diversification of gap junction proteins (connexins) in the central nervous system and the concept of functional compartments
    Dermietzel, R
    [J]. CELL BIOLOGY INTERNATIONAL, 1998, 22 (11-12) : 719 - 730