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1.
Water Res ; 44(14): 4015-28, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20541787

ABSTRACT

There is a growing need for a better understanding of the biogeochemical dynamics involved in microbial U(VI) reduction due to an increasing interest in using biostimulation via electron donor addition as a means to remediate uranium contaminated sites. U(VI) reduction has been observed to be maximized during iron-reducing conditions and to decrease upon commencement of sulfate-reducing conditions. There are many unknowns regarding the impact of iron/sulfate biogeochemistry on U(VI) reduction. This includes Fe(III) availability as well as the microbial community changes, including the activity of iron-reducers during the uranium biostimulation period even after sulfate reduction becomes dominant. Column experiments were conducted with Old Rifle site sediments containing Fe-oxides, Fe-clays, and sulfate rich groundwater. Half of the columns had sediment that was augmented with small amounts of Fe(III) in the form of (57)Fe-goethite, allowing for a detailed tracking of minute changes of this added phase to study the effects of increased Fe(III) levels on the overall biostimulation dynamics. Mössbauer spectroscopy showed that the added (57)Fe-goethite was bioreduced only during the first thirty days of biostimultuion, after which it remained constant. Augmentation with Fe(III) had a significant effect on the total flux of electrons towards different electron acceptors; it suppressed the degree of sulfate reduction, had no significant impact on Geobacter-type bacterial numbers but decreased the bacterial numbers of sulfate reducers and affected the overall microbial community composition. The addition of Fe(III) had no noticeable effect on the total uranium reduction.


Subject(s)
Biodegradation, Environmental , Iron/chemistry , Sulfates/chemistry , Uranium/metabolism , Bacteria/metabolism , Decontamination/methods , Iron/pharmacology , Iron Compounds , Minerals , Oxidation-Reduction , Sulfates/pharmacology
2.
J Neuroendocrinol ; 17(3): 186-94, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15796771

ABSTRACT

Signal transducers and activators of transcription (STATs) are a family of transcription factors linked to class I cytokine receptors. In the present study, we investigated whether their distribution in the hypothalamus reflects the feedback regulation by growth hormone and what role they might play in the functioning of target neurones. We demonstrate that each of the seven known STATs has a distinct distribution in the hypothalamus. Notably, the STAT5 proteins, that are important in growth hormone (GH) and prolactin signalling in peripheral tissues, were expressed in somatostatin neurones of the periventricular nucleus and dopamine neurones of the arcuate nucleus. Because somatostatin neurones are regulated by feedback from circulating GH, we investigated the importance of STAT5 in these neurones. We demonstrate that STAT5b protein expression, similar to somatostatin mRNA, is sexually dimorphic in the periventricular nucleus of rats and mice. Furthermore, chronic infusion of male dwarf rats with GH increased the expression of STAT5b, while a single injection of GH into similar rats induced the phosphorylation of STAT5 proteins. The cellular abundance of somatostatin mRNA in STAT5b-deficient mice was significantly reduced in the periventricular nucleus, effectively reducing the sexually dimorphic expression. These results are consistent with the hypothesis that STAT5 proteins are involved in the feedback regulation of somatostatin neurones by GH, and that these neurones may respond to patterned GH secretion to reinforce sexual dimorphism in the GH axis.


Subject(s)
DNA-Binding Proteins/physiology , Growth Hormone/physiology , Hypothalamus/metabolism , Neurons/metabolism , Somatostatin/metabolism , Trans-Activators/physiology , Animals , DNA-Binding Proteins/deficiency , DNA-Binding Proteins/genetics , Disease Models, Animal , Dwarfism, Pituitary/metabolism , Feedback, Physiological/physiology , Female , Growth Hormone/deficiency , Hypothalamus/cytology , Male , Mice , Mice, Knockout , Midline Thalamic Nuclei/cytology , Midline Thalamic Nuclei/metabolism , Milk Proteins/genetics , Rats , Rats, Mutant Strains , STAT5 Transcription Factor , Sex Characteristics , Signal Transduction/genetics , Signal Transduction/physiology , Trans-Activators/deficiency , Trans-Activators/genetics
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