The triple A syndrome is a rare autosomal recessive disease caused by mutations in the AAAS gene, which encodes the nucleoporin ALADIN. Recently it was shown that ALADIN plays a role in the import of different factors into the nucleus, which prevent the cell from DNA damage and consecutive cell death under oxidative stress. In order to investigate the changes in differential gene expression in ALADIN-deficient or mutated cells under oxidative stress we used fibroblast cell cultures of triple A syndrome patients and compared these to controls.
View Article and Find Full Text PDFgamma-Aminobutyric acid (GABA) is an important regulatory factor of pituitary gland function, which in addition to hypothalamic neurons, can be derived from intrapituitary sources, ie, growth hormone (GH) cells of rat and monkey. We report that human pituitary glands also express 2 isoforms of the GABA-synthesizing enzyme glutamate decarboxylase (GAD 65; GAD 67), the vesicular GABA transporter (VGAT), and multiple subunits of GABA (A, B, and C) receptors. GABA production and storage occurs in GH cells, as demonstrated by cellular colocalization of immunoreactive GAD and VGAT in GH cells and by reverse transcription-polymerase chain reaction analysis of laser capture-microdissected immunostained GH cells.
View Article and Find Full Text PDFChem Pharm Bull (Tokyo)
November 2000
The alpha-diimine Fe2+ complexes, [Fe(phen)3]2+, [Fe(bpy)3]2+, and [Fe(terpy)2]2+, (phen: 1,10-phenanthroline, bpy: 2,2'-bipyridyl, terpy: alpha,alpha',alpha''-tripyridine) were intercalated into zirconium dihydrogenphosphate phosphate dihydrate (gamma-zirconium phosphate, gamma-ZrP), Zr(PO4)(H2PO4).2H2O. The rate of the intercalation, the molar ratio of Fe to Zr, was found to be 3.
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