Literature DB >> 11527426

Manifold reduction of moesin in fetal Down syndrome brain.

B Lubec1, R Weitzdoerfer, M Fountoulakis.   

Abstract

Moesin is a member of the ERM family and is involved in plasma membrane-actin cytoskeleton cross-linking, resulting cell adhesion, shape, and motility. Because moesin was shown to be highly expressed in growth cones and moesin/radixin suppression led to impaired structure and function of this key element in brain development, we tested the ERM family, ezrin, radixin, and moesin, in fetal Down syndrome (DS) cortex at the early second trimester. We applied two-dimensional gel electrophoresis with subsequent MALDI detection and identification of protein spots followed by quantification with specific software. Moesin was shown to be significantly and manifold reduced in fetal DS brain, whereas reduction of ezrin and radixin did not reach statistical significance. We therefore propose the involvement of moesin in developmental impairment of DS brain, including deteriorated arborisation, neuritic outgrowth, and neuronal migration. Furthermore, decreased moesin is the second F-actin bundling protein, besides drebrin, that is manifold reduced in fetal DS brain. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11527426     DOI: 10.1006/bbrc.2001.5520

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Proteomic analysis of six- and twelve-month hippocampus and cerebellum in a murine Down syndrome model.

Authors:  Guido N Vacano; David S Gibson; Abdullah Arif Turjoman; Jeremy W Gawryluk; Jonathan D Geiger; Mark Duncan; David Patterson
Journal:  Neurobiol Aging       Date:  2017-11-26       Impact factor: 4.673

2.  The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration.

Authors:  Franz Oswald; Patricia Klöble; André Ruland; David Rosenkranz; Bastian Hinz; Falk Butter; Sanja Ramljak; Ulrich Zechner; Holger Herlyn
Journal:  Front Cell Neurosci       Date:  2017-07-26       Impact factor: 5.505

3.  Advances on the understanding of the origins of synaptic pathology in AD.

Authors:  Pascale Nathalie Lacor
Journal:  Curr Genomics       Date:  2007-12       Impact factor: 2.236

4.  Brain enhancer activities at the gene-poor 5p14.1 autism-associated locus.

Authors:  Yukiko U Inoue; Takayoshi Inoue
Journal:  Sci Rep       Date:  2016-08-09       Impact factor: 4.379

  4 in total

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