Expression patterns of MLC1 protein in the central and peripheral nervous systems

被引:45
作者
Teijido, Oscar
Casaroli-Marano, Ricardo
Kharkovets, Tatjana
Aguado, Fernando
Zorzano, Antonio
Palacin, Manuel
Soriano, Eduardo
Martinez, Albert
Estevez, Raid
机构
[1] Univ Barcelona, Unitat Fisiol, E-08907 Barcelona, Spain
[2] Univ Barcelona, Fac Biol, Dept Biochem & Mol Biol, E-08907 Barcelona, Spain
[3] Inst Res Biomed, E-08907 Barcelona, Spain
[4] Univ Barcelona, Fac Biol, Dept Cell Biol, E-08028 Barcelona, Spain
[5] Univ Hamburg, ZMNH, D-20246 Hamburg, Germany
关键词
myelin; leukodystrophy; MLC; neuron; astrocyte; development; PNS;
D O I
10.1016/j.nbd.2007.01.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mutations in MLC1 cause megalencephalic leukoencephalopathy with subcortical cysts (MLC), a disorder characterized clinically by macrocephaly, deterioration of motor functions, epilepsy and mental decline. Recent studies have detected MLC1 mRNA and protein in astroglial processes. In addition, our group previously reported MLC1 expression in some neurons in the adult mouse brain. Here we performed an exhaustive study of the expression pattern of MLC1 in the developing mouse brain by means of optic and electron microscopy. In the central nervous system, MLC1 was detected mainly in axonal tracts early in development. In addition, MLC1 was also observed in the peripheral nervous system and in several sensory epithelia, as retina or saccula maculae. Post-embedding immunogold experiments indicated that MLC1 is localized in astrocyte-astrocyte junctions, but not in the perivascular membrane, indicating that MLC1 is not a component of the dystrophin-glycoprotein complex. In neurons, MLC1 is located at the plasma membrane and vesicular structures. Our data provide a mouse MLC1 expression map that could be useful to understand the phenotype of MLC patients, and suggested that MLC disease is caused by an astrocytic and a neuronal dysfunction. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 545
页数:14
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