Functional Inactivation of Drosophila GCK Orthologs Causes Genomic Instability and Oxidative Stress in a Fly Model of MODY-2

Maturity-onset diabetes of the young (MODY) type 2 is caused by heterozygous inactivating mutations in the gene encoding glucokinase (GCK), a pivotal enzyme for glucose homeostasis. In the pancreas GCK regulates insulin secretion, while in the liver it promotes glucose utilization and storage. We showed that silencing the Drosophila GCK orthologs Hex-A and Hex-C results in a MODY-2-like hyperglycemia. Targeted knock-down revealed that Hex-A is expressed in insulin producing cells (IPCs) whereas Hex-C is specifically expressed in the fat body. We showed that Hex-A is essential for insulin secretion and it is required for Hex-C expression. Reduced levels of either Hex-A or Hex-C resulted in chromosome aberrations (CABs), together with an increased production of advanced glycation end-products (AGEs) and reactive oxygen species (ROS). This result suggests that CABs, in GCK depleted cells, are likely due to hyperglycemia, which produces oxidative stress through AGE metabolism. In agreement with this hypothesis, treating GCK-depleted larvae with the antioxidant vitamin B6 rescued CABs, whereas the treatment with a B6 inhibitor enhanced genomic instability. Although MODY-2 rarely produces complications, our data revealed the possibility that MODY-2 impacts genome integrity.     

Synthesis of TiO2-Au composites by titania-nanorod-assisted generation of gold nanoparticles at aqueous/nonpolar interfaces

Hydrophobically coated anatase TiO(2) nanorods can assist the reduction of AuCl(4) (-)ions at aqueous/nonpolar solvent interfaces, which results in the generation of organic-soluble Au nanoparticles with tunable size in the absence of any metal ligands and/or phase-transfer agents. The titania-nanorod-driven modulation of interfacial energy and catalysis of gold nucleation provide straightforward access to nanocomposite solutions of TiO(2)-stabilized Au nanoparticles. Among colloidal approaches, this method represents a unique tool for the surfactantless, large-scale preparation of nanostructured semiconductor-metal hybrid systems with relevant technological potential in catalysis, photocatalysis, and charge-storage processes.     

Room temperature solvent-free synthesis of monodisperse magnetite nanocrystals

We have successfully demonstrated a facile, solvent-free synthesis of highly crystalline and monodisperse Fe3O4 nanocrystallites at ambient temperature avoiding any heating. Solid state reaction of inorganic Fe(ll) and Fe(ll) salts with NaOH was found to produce highly crystalline Fe3O4 nanoparticles. The reaction, if carried out in the presence of surfactant such as oleic acid-oleylamine adduct, generated monodisperse Fe3O4 nanocrystals extractable directly from the reaction mixture. The extracted nanoparticles were capable of forming self-assembled, two-dimensional and uniform periodic array. The new process utilizes inexpensive and nontoxic starting materials, and does not require a use of high boiling point and toxic solvents, thus is amenable to an environmentally desirable, large-scale synthesis of nanocrystals.     

Multi-branching carbon nanotubes via self-seeded catalysts

A novel multi-branching carbon nanotube (CNT) structure is synthesized by direct current plasma enhanced chemical vapor deposition. The structure consists of aligned CNTs which have branches of smaller diameters growing aligned along a direction perpendicular to the original CNT. The mechanism of branching is explained in terms of a self-seeding of Ni catalyst which is transferred by sputtering from the original catalyst particles in the backbone CNTs to the walls of those CNTs. It is also shown that the branching induced a large increase in surface area and total nanotube length and can be beneficial in supporting very fine Pt nanoparticles for fuel cell and other catalytic applications. Such an array of Y-junction nanostructures could be useful for the fabrication of a high-density array of nanoelectronics switches and transistors.     

Nanoparticles from polylactide and polyether block copolymers: formation, properties, encapsulation, and release of pyrene--fluorescent model of hydrophobic drug

Polylactide-b-polyglycidol-b-poly(ethylene oxide) terpolymers and their derivatives with carboxyl and 4-(phenylazo)phenyl labels in polyglycidol blocks were used for formation of nanoparticles. Nanoparticles were produced by self assembly of terpolymer macromolecules in water above the critical aggregation concentration and by dialysis of terpolymer solutions in 1,4-dioxane against water. For terpolymers with 4-(phenylazo)phenyl labels critical aggregation concentrations increased after irradiation with UV light (300 < lambda < 400 nm) inducing conformational change of the label from trans- to cis-conformation. Diameters of nanoparticles obtained by self-assembly of macromolecules ranged from 20 to 44 nm. Dialysis yielded nanoparticles with bimodal diameter distribution. One fraction had diameters below 35 nm and diameters of the second fraction were in a range from 350 to 2300 nm, depending on terpolymer structure. Mixtures of terpolymers with poly(L,L-lactide) and poly(D,D-lactide) blocks yielded nanoparticles with diameters from 350 to 440 nm. Pyrene was incorporated into nanoparticles by partition between solution and nanoparticles or directly during particle formation by dialysis. Monitoring of pyrene release from nanoparticles suggests that a fraction of this compound was entrapped into the polylactide core whereas the remaining one was located in the polyether rich shell. The release from shells is faster for nanoparticles made from copolymers with carboxyl labels in polyglycidol blocks.     

Propagation of highly nonlinear solitary waves in a curved granular chain

We assemble granular chains composed of spheres of uniform diameter in different curved configurations. We study the properties of highly nonlinear solitary waves traveling in the curved channels as a function of the curve angle and of the radius of curvature, using experiments and numerical simulations. We observe that solitary waves propagate robustly even under drastic deflection, such as $90^{\circ }$ and $180^{\circ }$ turns. When the solitary waves encounter a sharp turn with a radius of curvature as small as one spherical particle’s diameter, we report the formation of secondary solitary waves resulting from the interaction with the guiding rail. We compare experimental results with numerical simulations based on a discrete element model that accounts for nonlinear and dissipative interactions between particles. This study demonstrates that granular chains are efficient wave-guides, even in complex geometrical configurations. Moreover, the findings in this study suggest that solitary waves could be used as novel information and/or energy carriers.     

Columnar Fe2O3 arrays via plasma-enhanced growth: Interplay of fluorine substitution and photoelectrochemical properties

A single-step plasma enhanced-chemical vapor deposition (PE-CVD) route for the synthesis of F-doped iron(III) oxide nanomaterials is presented. Growth experiments, performed from a fluorinated Fe(II) β-diketonate precursor on Indium Tin Oxide (ITO) between 200 and 400 °C, yielded columnar β-Fe₂O₃ arrays with a preferential (100) growth direction. The fluorine content in the deposits could be adjusted by the sole variation of the deposition temperature controlling, in turn, the optical absorption and energy bandgap. Photocurrent measurements and Mott–Schottky analyses, carried out in Na₂SO₄ solution under one sun illumination, evidenced a conductivity switch from n- to p-type upon increasing fluorine amount in the obtained nanomaterials. The sample photocurrent density, donor content and flatband potential support the hypothesis that a progressive substitution of oxygen by fluorine in the iron(III) oxide lattice can alter electronic structure and extend charge carrier lifetimes, making anion-doped β-Fe₂O₃ an efficient water oxidation catalyst.     

An empirical approach to compare the performance of heterogeneous academic fields

In this paper, we propose a ‘scaling’ approach to compare the scientific performance of Italian heterogeneous academic disciplines. This method is based on the idea that, after eliminating the percentages of ‘silent’ researchers, the distribution of bibliometric parameters of the different academic fields can be superimposed and collapse into a unique master curve by a single scaling parameter. By using data on the scientific production of around 2,500 scholars of the university of Rome ‘La Sapienza’ from the Web of Science from 2004 to 2008, we (i) demonstrate the existence of a master curve, (ii) determine the scaling factors that work like rates of substitution to compare the scientific production across different academic fields on a common ground, (iii) show that the master bibliometric distribution follows a log-normal law and (iv) illustrate the relevance of the proposed approach for research assessment and allocation of competitive funding at the university level.     

Washcoating of low surface area cerium oxide on complex geometry substrates

ABSTRACT

An acid-free formulation based on water, glycerol, and polyvinyl alcohol (PVA) was studied to disperse and stabilize, via steric-like interaction, low surface area cerium oxide powders. A dispersion route that implies a milling process and a proper ratio among the components was experienced. PVA was used as viscosity modulator, to enhance viscosity and system stability. Newtonian fluids, suitable for foams dip-coating, were obtained in the application shear range. Foams with different porosities (20, 30, and 40 pore per inch density) were coated. It was found that withdrawal velocity did not affect deposition: a constancy in coating load was obtained once rheology was fixed, while multiple dipping was effective to enhance load. An optimal flash drying temperature (350°C) was identified to consolidate the coated layer and to decompose the organic additives. Good loads, homogeneous coverage, and no pore clogging were obtained after calcination at 900°C. Even though acceptable weight losses were obtained, further investigations need to be accomplished to understand data scattering after adhesion tests.