Reduction of actin-related protein complex 2/3 in fetal Down syndrome brain

被引:76
作者
Weitzdoerfer, R
Fountoulakis, M
Lubec, G
机构
[1] Univ Vienna, Dept Pediat, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Neonatol, A-1090 Vienna, Austria
[3] F Hoffmann La roche, CH-4070 Basel, Switzerland
关键词
actin; cytoskeleton; actin binding proteins; coronin-like protein p57; actin-related protein complex 2/3 (Arp2/3) 20 kDa subunit; fetal; Down syndrome;
D O I
10.1016/S0006-291X(02)00291-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Down syndrome (DS) patients present with morphological abnormalities in brain development, leading to mental retardation. Given the importance of actin cytoskeleton to form the basis of various cell functions, the regulation of actin system is crucial during brain development. We therefore aimed to study the expression levels of actin binding proteins in fetal DS and control cortex. We evaluated the levels of eight actin binding proteins using the proteomic approach of two-dimensional gel electrophoresis with subsequent mass spectroscopical identification of protein spots. In fetal DS brain we found a significant reduction of the actin-related protein complex 2/3 (Arp2/3) 20 kDa subunit and the coronin-like protein p57, which are involved in actin filament cross-linking and nucleation and capping of actin filaments. We conclude that deficient levels of these proteins may, at least partially, be involved in the dysgenesis of the brain in DS. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:836 / 841
页数:6
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