Calibrating and testing tissue equivalent proportional counters with 37Ar

A method for testing and calibrating tissue equivalent proportional counters with37Ar is described.37Ar is produced by exposure of argon in its normal isotope composition to thermal neutrons. It is shown that - up to volume ratios of 0.01 of argon to the tissue equivalent gas - there is no appreciable effect of the argon admixture on the function of the proportional counter. Conventional calibration methods with characteristic x-rays or with -particles require modifications of the detectors, and they test only small sub-volumes in the counters. In contrast, argon permits calibrations and tests of the resolution that are representative for the entire counter volume and that do not require changes in detector construction. The method is equally applicable to multi-element proportional counters; it is here exemplified by its application to a long cylindrical counter of simplified design that is part of such a multi-element configuration

Making archaeology abroad. A postcolonial perspective in Malta

This research is about the archaeological making of the Tas-Silġ site in Malta. Archaeological investigations in Tas-Silġ have been mainly carried out by a foreign research entity (Missione Archeologica Italiana a Malta). This research explores nature, development and impact of the Italian project within the wider context of Maltese political and archaeological decolonisation. To unpack the making of the Tas-Silġ site, this study looks into the micro politics of the archaeological process and unravels the tensions that have accompanied it. In particular this study: 1) microexcavates the convoluted process that established and maintained an Italian research team as privileged interpret of the archaeology in Tas- Silġ; 2) assesses impacts and relevance of this long-term Italian project in postcolonial Malta; and 3) examines how archaeological process and site layout interact to produce forms of intellectual and physical dislocation. The research adopts a qualitative approach to give voice to the whole gamut of participants that have defined, negotiated and challenged the making of Tas-Silġ. The research shows that Missione control over the site and the archaeological knowledge derived from its investigations is highly controversial. However it reaches the conclusion that Missione involvement in Malta cannot be assessed against binary categories of local/foreigner and colonial/postcolonial although those elements have a role in defining this association. In addressing the situated complexity of making archaeology in Tas-Silġ, this research sets up a space of discussion on the ambivalence of foreign archaeology in decolonised countries

Methylglyoxal-dependent glycative stress and deregulation of SIRT1 functional network in the ovary of PCOS mice

Advanced glycation end-products (AGEs) are involved in the pathogenesis and consequences of polycystic ovary syndrome (PCOS), a complex metabolic disorder associated with female infertility. The most powerful AGE precursor is methylglyoxal (MG), a byproduct of glycolysis, that is detoxified by the glyoxalase system. By using a PCOS mouse model induced by administration of dehydroepiandrosterone (DHEA), we investigated whether MG-dependent glycative stress contributes to ovarian PCOS phenotype and explored changes in the Sirtuin 1 (SIRT1) functional network regulating mitochondrial functions and cell survival. In addition to anovulation and reduced oocyte quality, DHEA ovaries revealed altered collagen deposition, increased vascularization, lipid droplets accumulation and altered steroidogenesis. Here we observed increased intraovarian MG-AGE levels in association with enhanced expression of receptor for AGEs (RAGEs) and deregulation of the glyoxalase system, hallmarks of glycative stress. Moreover, DHEA mice exhibited enhanced ovarian expression of SIRT1 along with increased protein levels of SIRT3 and superoxide dismutase 2 (SOD2), and decreased peroxisome proliferator-activated receptor gamma co-activator 1 alpha (PGC1 alpha), mitochondrial transcriptional factor A (mtTFA) and translocase of outer mitochondrial membrane 20 (TOMM20). Finally, the presence of autophagy protein markers and increased AMP-activated protein kinase (AMPK) suggested the involvement of SIRT1/AMPK axis in autophagy activation. Overall, present findings demonstrate that MG-dependent glycative stress is involved in ovarian dysfunctions associated to PCOS and support the hypothesis of a SIRT1-dependent adaptive response

Analyses of Ligand Binding to IP3 Receptors Using Fluorescence Polarization.

Fluorescence polarization (FP) can be used to measure binding of a small fluorescent ligand to a larger protein because the ligand rotates more rapidly in its free form than when bound. When excited with plane polarized light, the free fluorescent ligand emits depolarized light, which can be quantified. Upon binding, its rotation is reduced and more of the emitted light remains polarized. This allows FP to be used as a nondestructive assay of ligand binding. Here we describe a fast, high-throughput FP assay to quantify the binding of fluorescently labeled inositol 1,4,5-trisphosphate (IP3) to N-terminal fragments of the IP3 receptor. The assay is fast (1-6 h), it avoids use of radioactive materials and when measurements are performed at different temperatures, it can resolve Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) changes of ligand binding

Albumin and fibronectin adsorption on treated titanium surfaces for osseointegration: An advanced investigation

Protein adsorption has a central role in the outcome of implants. However, there is no consensus about the impact of the different surface properties on the material-protein interactions. Here, the adsorption of albumin and fibmnectin in near-physiological concentration is investigated on three differently treated titanium-based surfaces and compared after a thorough characterization. The different titanium surfaces have very different surface properties, in particular regarding roughness, oxide porosity, wettability, surface energy, and zeta potential, which are all known to deeply affect protein adsorption. By merging several characterization techniques, some conventional and some innovative, it was possible to discriminate the effect of surface properties on different aspects of protein adsorption. Despite forming a continuous layer on all samples, the amount of proteins bound to the surface is mainly due to surface roughness and topography, which can overcome the effect of wettability and surface energy. On the other hand, the secondary structure of albumin and fibmnectin and their orientation are determined by the hydroxyl groups exposed on the surfaces, depending on their surface concentration and acidic reactivity in the former, and the surface zeta potential in the latter

Radially restricted linear energy transfer for high-energy protons: A new analytical approach

Radially restricted linear energy transfer (LET) is a basic physical parameter relevant to radiation biology and radiation protection. In this report a convenient method is presented for the analytical computation of this quantity without the need for complicated simulation. The method uses the energy-re-stricted LETL, as recently redefined in a 1993 ICRU draft document and supplements it by a relatively simple term that represents the energy of fast rays lost within distancer from the track core. The method provides a better fit than other models and is valid over the entire range of radial distance from track center to the maximum radial distance traveled by the most energetic secondary electrons.L r computed by this approach differs only a few percent from the values Contribution to the international symposium on heavy ions research: space, radiation protection and therapy, 21–24 March 1994, Sophia-Antipolis, Franc

Timing temporal transitions during brain development

During development a limited number of progenitors generate diverse cell types that comprise the nervous system. Neuronal diversity, which arises largely at the level of neural stem cells, is critical for brain function. Often these cells exhibit temporal patterning: they sequentially produce neurons of distinct cell fates as a consequence of intrinsic and/or extrinsic cues. Here, we review recent advances in temporal patterning during neuronal specification, focusing on conserved players and mechanisms in invertebrate and vertebrate models. These studies underscore temporal patterning as an evolutionarily conserved strategy to generate neuronal diversity. Understanding the general principles governing temporal patterning and the molecular players involved will improve our ability to direct neural progenitors towards specific neuronal fates for brain repair