Dall’Archivio Bompiani : pagine illustrate nell’editoria d’arte dei primi anni Quaranta

Tra la fine degli anni Trenta e i primi anni Quaranta nel panorama dell\u2019editoria d\u2019arte italiana emersero nuovi orientamenti, specchio del decisivo impulso conosciuto dalle tecnologie di riproduzione e di stampa fotomeccanica delle immagini e, al contempo, di una moderna sensibilit\ue0 visiva. Promotore di innovative strategie editoriali fondate sul valore della qualit\ue0 tipografica della pagina illustrata, Valentino Bompiani risulta avere un ruolo chiave in queste vicende. Attraverso il vaglio e l\u2019analisi di materiali d\u2019archivio inediti, l\u2019intervento intende mettere a fuoco il contributo dell\u2019editore e dei suoi collaboratori nella definizione di un nuovo modo di comunicare l\u2019arte \u2013 dall\u2019episodio di \uabCivilt\ue0. Rivista Bimestrale della Esposizione Universale di Roma\ubb, alla pionieristica collana di monografie Apologie dei capolavori dell\u2019arte italiana riprodotti nelle misure originali \u2013 aprendo la strada a problemi che avrebbero connotato il profilo dell\u2019industria editoriale del Dopoguerra

Lo Studio d’Arte Palma : storia di un’impresa per il commercio artistico nell’Italia del dopoguerra

Inaugurato a Roma nel maggio 1944, a poche settimane dalla Liberazione, lo Studio d\u2019Arte Palma ha costituito un inedito esperimento di organizzazione artistica capace di coniugare attivit\ue0 espositive, mercantili e di centro di restauro, nell\u2019ottica congiunta di un\u2019esigenza di valorizzazione del patrimonio e delle produzioni d\u2019arte italiane e della proposta di un nuovo gusto, espressione dei valori del mondo contemporaneo. Questo contributo intende, per la prima volta, tracciarne il profilo, mettendo in luce la specificit\ue0 dell\u2019iniziativa nel coevo panorama delle gallerie d\u2019arte. A partire dall\u2019analisi delle fonti d\u2019archivio, si precisano la storia, la progettualit\ue0 e la programmazione della \u201cPalma\u201d, a cui collaborarono, raccolte attorno alla figura del suo fondatore, Pietro Maria Bardi, alcune tra le personalit\ue0 di maggiore rilievo del sistema delle arti del tempo.Opened in Rome in May 1944, a few weeks before the Liberation, Studio d\u2019Arte Palma has been an innovative experiment of artistic organization aimed at combining exhibition, trade and conservation activities. Its orientation, beside answering the need of Italian heritage and art production enhancement, supported the proposal of a new taste, expression of contemporary values. This essay aims to outline the profile of \u201cPalma\u201d, pointing out the specificity of the project in the coeval panorama of art galleries. Starting from the analysis of archival sources, the study investigates the history, the organization and the planning of Studio d\u2019Arte Palma, which gathered some of the most relevant personalities of the postwar art system around the person of its founder, Pietro Maria Bardi

MHD simulations of plasma dynamics in pinch discharges in capillary plasmas

Magnetohydrodynamic simulation results related to the capillary discharge dynamics are presented. The main physical process that should be taken into account is the ablation of the capillary wall material evaporated by the heat flux from the capillary plasma. The possible applications of the capillary discharges related to the physics of the X-ray lasers and the use of the capillary plasma to provide a guiding for ultrashort high-intensity laser pulses over a distance greater than the defocusing length are discussed

The nasal delivery of nanoencapsulated statins – An approach for brain delivery

© 2016 Clementino et al. Purpose: Along with their cholesterol-lowering effect, statins have shown a wide range of pleiotropic effects potentially beneficial to neurodegenerative diseases. However, such effects are extremely elusive via the conventional oral administration. The purpose of the present study was to prepare and characterize the physicochemical properties and the in vivo biodistribution of simvastatin-loaded lecithin/chitosan nanoparticles (SVT-LCNs) suitable for nasal administration in view of an improved delivery of the statins to the brain. Materials and methods: Chitosan, lecithin, and different oil excipients were used to prepare nanocapsules loaded with simvastatin. Particle size distribution, surface charge, structure, simvastatin loading and release, and interaction with mucus of nanoparticles were determined. The nanoparticle nasal toxicity was evaluated in vitro using RPMI 2651 nasal cell lines. Finally, in vivo biodistribution was assessed by gamma scintigraphy via Tc99m labeling of the particles. Results: Among the different types of nanoparticles produced, the SVT-LCN_MaiLab showed the most ideal physicochemical characteristics, with small diameter (200 nm), positive surface charge (+48 mV) and high encapsulation efficiency (EE; 98%). Size distribution was further confirmed by nanoparticle tracking analysis and electron microscopy. The particles showed a relatively fast release of simvastatin in vitro (35.6%±4.2% in 6 hours) in simulated nasal fluid. Blank nanoparticles did not show cytotoxicity, evidencing that the formulation is safe for nasal administration, while cytotoxicity of simvastatin-loaded nanoparticles (IC50) was found to be three times lower than the drug solution (9.92 vs 3.50 μM). In rats, a significantly higher radioactivity was evidenced in the brain after nasal delivery of simvastatin-loaded nanoparticles in comparison to the administration of a similar dose of simvastatin suspension. Conclusion: The SVT-LCNs developed presented some of the most desirable characteristics for mucosal delivery, that is, small particle size, positive surface charge, long-term stability, high EE, and mucoadhesion. In addition, they displayed two exciting features: First was their biodegradability by enzymes present in the mucus layer, such as lysozyme. This indicates a new Trojan-horse strategy which may enhance drug release in the proximity of the nasal mucosa. Second was their ability to enhance the nose-to-brain transport as evidenced by preliminary gamma scintigraphy studies

Self-dual gravitational instantons and geometric flows of all Bianchi types

We investigate four-dimensional, self-dual gravitational instantons endowed with a product structure RxM_3, where M_3 is homogeneous of Bianchi type. We analyze the general conditions under which Euclidean-time evolution in the gravitational instanton can be identified with a geometric flow of a metric on M_3. This includes both unimodular and non-unimodular groups, and the corresponding geometric flow is a general Ricci plus Yang-Mills flow accompanied by a diffeomorphism.Comment: Latex, 12 pages; Final versio

The PLASMONX Project for advanced beam physics experiments

The Project PLASMONX is well progressing into its design phase and has entered as well its second phase of procurements for main components. The project foresees the installation at LNF of a Ti:Sa laser system (peak power > 170 TW), synchronized to the high brightness electron beam produced by the SPARC photo-injector. The advancement of the procurement of such a laser system is reported, as well as the construction plans of a new building at LNF to host a dedicated laboratory for high intensity photon beam experiments (High Intensity Laser Laboratory). Several experiments are foreseen using this complex facility, mainly in the high gradient plasma acceleration field and in the field of mono- chromatic ultra-fast X-ray pulse generation via Thomson back-scattering. Detailed numerical simulations have been carried out to study the generation of tightly focused electron bunches to collide with laser pulses in the Thomson source: results on the emitted spectra of X-rays are presented

Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons

Spinal muscular atrophy is a motor neuron disorder caused by mutations in SMN1. The reasons for the selective vulnerability of motor neurons linked to SMN (encoded by SMN1) reduction remain unclear. Therefore, we performed deep RNA sequencing on human spinal muscular atrophy motor neurons to detect specific altered gene splicing/expression and to identify the presence of a common sequence motif in these genes. Many deregulated genes, such as the neurexin and synaptotagmin families, are implicated in critical motor neuron functions. Motif-enrichment analyses of differentially expressed/spliced genes, including neurexin2 (NRXN2), revealed a common motif, motif 7, which is a target of SYNCRIP. Interestingly, SYNCRIP interacts only with full-length SMN, binding and modulating several motor neuron transcripts, including SMN itself. SYNCRIP overexpression rescued spinal muscular atrophy motor neurons, due to the subsequent increase in SMN and their downstream target NRXN2 through a positive loop mechanism and ameliorated SMN-loss-related pathological phenotypes in Caenorhabditis elegans and mouse models. SMN/SYNCRIP complex through motif 7 may account for selective motor neuron degeneration and represent a potential therapeutic target

Signatures of Environmental Genetic Adaptation Pinpoint Pathogens as the Main Selective Pressure through Human Evolution

Previous genome-wide scans of positive natural selection in humans have identified a number of non-neutrally evolving genes that play important roles in skin pigmentation, metabolism, or immune function. Recent studies have also shown that a genome-wide pattern of local adaptation can be detected by identifying correlations between patterns of allele frequencies and environmental variables. Despite these observations, the degree to which natural selection is primarily driven by adaptation to local environments, and the role of pathogens or other ecological factors as selective agents, is still under debate. To address this issue, we correlated the spatial allele frequency distribution of a large sample of SNPs from 55 distinct human populations to a set of environmental factors that describe local geographical features such as climate, diet regimes, and pathogen loads. In concordance with previous studies, we detected a significant enrichment of genic SNPs, and particularly non-synonymous SNPs associated with local adaptation. Furthermore, we show that the diversity of the local pathogenic environment is the predominant driver of local adaptation, and that climate, at least as measured here, only plays a relatively minor role. While background demography by far makes the strongest contribution in explaining the genetic variance among populations, we detected about 100 genes which show an unexpectedly strong correlation between allele frequencies and pathogenic environment, after correcting for demography. Conversely, for diet regimes and climatic conditions, no genes show a similar correlation between the environmental factor and allele frequencies. This result is validated using low-coverage sequencing data for multiple populations. Among the loci targeted by pathogen-driven selection, we found an enrichment of genes associated to autoimmune diseases, such as celiac disease, type 1 diabetes, and multiples sclerosis, which lends credence to the hypothesis that some susceptibility alleles for autoimmune diseases may be maintained in human population due to past selective processes

Ebf factors and MyoD cooperate to regulate muscle relaxation via Atp2a1

Jin, Saihong et al.Myogenic regulatory factors such as MyoD and Myf5 lie at the core of vertebrate muscle differentiation. However, E-boxes, the cognate binding sites for these transcription factors, are not restricted to the promoters/enhancers of muscle cell-specific genes. Thus, the specificity in myogenic transcription is poorly defined. Here we describe the transcription factor Ebf3 as a new determinant of muscle cell-specific transcription. In the absence of Ebf3 the lung does not unfold at birth, resulting in respiratory failure and perinatal death. This is due to a hypercontractile diaphragm with impaired Ca2+ efflux-related muscle functions. Expression of the Ca2+ pump Serca1 (Atp2a1) is downregulated in the absence of Ebf3, and its transgenic expression rescues this phenotype. Ebf3 binds directly to the promoter of Atp2a1 and synergises with MyoD in the induction of Atp2a1. In skeletal muscle, the homologous family member Ebf1 is strongly expressed and together with MyoD induces Atp2a1. Thus, Ebf3 is a new regulator of terminal muscle differentiation in the diaphragm, and Ebf factors cooperate with MyoD in the induction of muscle-specific genes. © 2014 Macmillan Publishers Limited.This work was supported by grants from the German Research Foundation (DFG, TRR54; FOR1586; FOR2033) and by a stipend of the Max Planck SocietyPeer Reviewe

Mitragynine Attenuates Withdrawal Syndrome in Morphine-Withdrawn Zebrafish

A major obstacle in treating drug addiction is the severity of opiate withdrawal syndrome, which can lead to unwanted relapse. Mitragynine is the major alkaloid compound found in leaves of Mitragyna speciosa, a plant widely used by opiate addicts to mitigate the harshness of drug withdrawal. A series of experiments was conducted to investigate the effect of mitragynine on anxiety behavior, cortisol level and expression of stress pathway related genes in zebrafish undergoing morphine withdrawal phase. Adult zebrafish were subjected to two weeks chronic morphine exposure at 1.5 mg/L, followed by withdrawal for 24 hours prior to tests. Using the novel tank diving tests, we first showed that morphine-withdrawn zebrafish display anxiety-related swimming behaviors such as decreased exploratory behavior and increased erratic movement. Morphine withdrawal also elevated whole-body cortisol levels, which confirms the phenotypic stress-like behaviors. Exposing morphine-withdrawn fish to mitragynine however attenuates majority of the stress-related swimming behaviors and concomitantly lower whole-body cortisol level. Using real-time PCR gene expression analysis, we also showed that mitragynine reduces the mRNA expression of corticotropin releasing factor receptors and prodynorphin in zebrafish brain during morphine withdrawal phase, revealing for the first time a possible link between mitragynine's ability to attenuate anxiety during opiate withdrawal with the stress-related corticotropin pathway