Distribution and cellular localization of adrenoleukodystrophy protein in human tissues:: Implications for X-linked adrenoleukodystrophy

被引:44
|
作者
Hoeftberger, Romana
Kunze, Markus
Weinhofer, Isabelle
Aboul-Enein, Faluny
Voigtlaender, Till
Oezen, Iris
Amann, Gabriele
Bernheimer, Hanno
Budka, Herbert
Berger, Johannes
机构
[1] Med Univ Vienna, Inst Neurol, A-1097 Vienna, Austria
[2] Med Univ Vienna, Ctr Brain Res, Vienna, Austria
[3] Med Univ Vienna, Dept Clin Pathol, Vienna, Austria
[4] SMZ Ost Danube Hosp, Dept Neurol, Vienna, Austria
关键词
adrenoleukodystrophy protein (ALDP); X-ALD; pituitary gland; brain; cortisol; proopiomelanocortin (POMC);
D O I
10.1016/j.nbd.2007.07.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Defects of adrenoleukodystrophy protein (ALDP) lead to X-linked adrenoleukodystrophy (X-ALD), a disorder mainly affecting the nervous system white matter and the adrenal cortex. In the present study, we examine the expression of ALDP in various human tissues and cell lines by multiple-tissue RNA expression array analysis, Western blot analysis, and immunohistochemistry. ALDP-encoding mRNA is most abundant in tissues with high energy requirements such as heart, muscle, liver, and the renal and endocrine systems. ALDP selectively occurs in specific cell types of brain (hypothalamus and basal nucleus of Meynert), kidney (distal tubules), skin (eccrine gland, hair follicles, and fibroblasts), colon (ganglion cells and epithelium), adrenal gland (zona reticularis and fasciculata), and testis (Sertoli and Leydig cells). In pituitary gland, ALDP is confined to adrenocorticotropin-producing cells and is significantly reduced in individuals receiving long term cortisol treatment. This might indicate a functional link between ALDP and proopiomelanocortin-derived peptide hormones. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:165 / 174
页数:10
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