356 research outputs found

    Growth of ZnO nanolayers inside the capillaries of photonic crystal fibres

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    In this study, we describe the formation of ZnO nanolayers inside the air capillaries of a silica photonic crystal fibre (PCF), targeting random laser and organic vapor sensing applications. ZnO nanolayers were developed by infiltrating the capillaries of the silica PCF with Zn-acetate/methanol solutions of various concentrations, followed by annealing treatments. The growth and morphology of the synthesized ZnO nanolayers were characterized by means of scanning electron microscopy (SEM) and found to be affected by the concentration of the Zn-acetate/methanol infiltration solution. For low concentrations, inspection with SEM revealed the formation of 25 and 100-nm-thick ZnO nanolayers across the entire length of the infiltrated capillaries, whereas increasing the Zn-acetate concentration resulted to the formation of randomly placed isolated ZnO nanorods. Room temperature photoluminescence spectra of the ZnO nanolayers inside the PCF were measured and compared with the corresponding spectra reported for ZnO structures formed on typical surfaces.Comment: 5 pages, 5 figures, Available online 29 June 2013, in press. Thin Solid Film, Elsevier, Available online 29 June 201

    The meaning of the architectural form of the tower: the ancient towers of Siphnos

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    The phenomenon of building numerous towers in Siphnos and also in other Hellenic regions in antiquity (sixth to fourth century BC) has been studied only relatively recently by scholars. Their number, the quality of the cture, and the constant typology of these towers, contest the suggested theories about their original purpose.In this study, the analysis of the towers addresses not just the structure of the building but also the ning that has been attributed to the space and the form. This research is an attempt to detect the architectural ities that render the tower capable of corresponding to specific requirements and to fulfilling the intentions their creators.The analysis of the meaning and the intentions which prompted the selection of the particular architectural eidos, is derived from the perceptions and beliefs of that era in terms of its social, religious, philosophical and technological contexts. The results of the phenomenological analysis have been confirmed further supported from by historical, religious and anthropological research.The research proposes that the towers of Siphnos have had a multivalent connection with the mines ch can be interpreted as sacred and functional. The vegetation and generation of metals, ores and minerals considered as a certain fact in antiquity. The regeneration of all creatures presupposed the ceremonial repetition of the sacred coitus of the primordial couple in the ritual known as "hieros gamos". The tower is the ptor, the intermediary vehicle in the performance of this holy marriage, attracting thunderbolts that constitute the sign of this union. Also, the towers define and demarcate the metallurgical region and shape the geographical networks in accordance with the entries of the galleries, in order to construct their specific ntated directions. The capability of the towers in attracting lightning, has served positively the safety of the e workers and mines. The fact that all the towers stand on surface metalliferous veins, as was expected, rding to renaissance texts, answers the unsolved problem of the placing of the towers around the island and firms the verification of the proposed theory

    Induction of IL-4R alpha-dependent microRNAs identifies PI3K/Akt signaling as essential for IL-4-driven murine macrophage proliferation in vivo

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    Macrophage (MΦ) activation must be tightly controlled to preclude overzealous responses that cause self-damage. MicroRNAs promote classical MΦ activation by blocking antiinflammatory signals and transcription factors but also can prevent excessive TLR signaling. In contrast, the microRNA profile associated with alternatively activated MΦ and their role in regulating wound healing or antihelminthic responses has not been described. By using an in vivo model of alternative activation in which adult Brugia malayi nematodes are implanted surgically in the peritoneal cavity of mice, we identified differential expression of miR-125b-5p, miR-146a-5p, miR-199b-5p, and miR-378-3p in helminth-induced MΦ. In vitro experiments demonstrated that miR-378-3p was specifically induced by IL-4 and revealed the IL-4–receptor/PI3K/Akt-signaling pathway as a target. Chemical inhibition of this pathway showed that intact Akt signaling is an important enhancement factor for alternative activation in vitro and in vivo and is essential for IL-4–driven MΦ proliferation in vivo. Thus, identification of miR-378-3p as an IL-4Rα–induced microRNA led to the discovery that Akt regulates the newly discovered mechanism of IL-4–driven macrophage proliferation. Together, the data suggest that negative regulation of Akt signaling via microRNAs might play a central role in limiting MΦ expansion and alternative activation during type 2 inflammatory settings

    Encapsulation of cationic iridium(iii) tetrazole complexes into a silica matrix: Synthesis, characterization and optical properties

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    Herein we report the easy incorporation of brightly phosphorescent cationic iridium(iii) tetrazole complexes into a silica based matrix via an easily scalable colloidal process. For this purpose, two cationic Ir(iii) emitters bearing 5-aryl tetrazole ligands (R-CN4) were selected: blue [F2IrPTZ-Me]+(C^N = F2ppy; N^N = PTZ-Me-2-(2-methyl-2H-tetrazol-5-yl)pyridine) and red [IrQTZ-Me]+(C^N = ppy; N^N = QTZ-Me-2-(2-methyl-2H-tetrazol-5-yl)quinoline). The cationic complexes were readily adsorbed to negatively charged silica nanoparticles and trapped in the sol-gel matrix. The sol-to-solid phase transfer was performed by using an innovative spray-freeze-drying technique, leading to the formation of phosphorescent solid micro-granules. The structural and optical characterisation of the Ir(iii) complexes together with SiO2nanoparticles, nanosols (Ir@SiO2) and powders (Ir@SiO2powders), revealed how the presence of the Ir(iii)-based complexes did not alter the morphology of the colloidal silica or granulated phases. Moreover, the silica matrix did not interfere with the optical properties of the embedded complexes. The distribution of [F2IrPTZ-Me]+and [IrQTZ-Me]+in the spray-freeze-dried powders was qualitatively evaluated by fluorescence microscopy, revealing how the luminescent particles were homogeneously dispersed all over the silica matrix. Interestingly, in aqueous solution the release of complex [F2IrPTZ-Me]+from the corresponding Ir@SiO2powder is almost negligible, therefore suggesting that a strong interaction occurs between the host-silica matrix and the Ir(iii) guest complex

    Listeria monocytogenes Infection in Macrophages Induces Vacuolar-Dependent Host miRNA Response

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    Listeria monocytogenes is a Gram-positive facultative intracellular pathogen, causing serious illness in immunocompromised individuals and pregnant women. Upon detection by macrophages, which are key players of the innate immune response against infection, L. monocytogenes induces specific host cell responses which need to be tightly controlled at transcriptional and post-transcriptional levels. Here, we ask whether and how host miRNAs, which represent an important mechanism of post-transcriptional regulation in a wide array of biological processes, are altered by a model pathogen upon live infection of murine bone marrow derived macrophages. We first report that L. monocytogenes subverts the host genome-wide miRNA profile of macrophages in vitro. Specifically, we show that miR-155, miR-146a, miR-125a-3p/5p and miR-149 were amongst the most significantly regulated miRNAs in infected macrophages. Strikingly, these miRNAs were highly upregulated upon infection with the Listeriolysin-deficient L. monocytogenes mutant Δhly, that cannot escape from the phagosome thus representing a vacuolar-contained infection. The vacuolar miRNA response was significantly reduced in macrophages deficient for MyD88. In addition, miR-146a and miR-125a-3p/5p were regulated at transcriptional levels upon infection, and miR-125a-3p/5p were found to be TLR2 responsive. Furthermore, miR-155 transactivation in infection was regulated by NF-κB p65, while miR-146a and miR-125a-3p/5p expression was unaffected in p65-deficient primary macrophages upon L. monocytogenes infection. Our results demonstrate that L. monocytogenes promotes significant changes in the miRNA expression profile in macrophages, and reveal a vacuolar-dependent miRNA signature, listeriolysin-independent and MyD88-dependent. These miRNAs are predicted to target immune genes and are therefore most likely involved in regulation of the macrophage innate immune response against infection at post-transcriptional levels

    The impact of stress on tumor growth: peripheral CRF mediates tumor-promoting effects of stress

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    <p>Abstract</p> <p>Introduction</p> <p>Stress has been shown to be a tumor promoting factor. Both clinical and laboratory studies have shown that chronic stress is associated with tumor growth in several types of cancer. Corticotropin Releasing Factor (CRF) is the major hypothalamic mediator of stress, but is also expressed in peripheral tissues. Earlier studies have shown that peripheral CRF affects breast cancer cell proliferation and motility. The aim of the present study was to assess the significance of peripheral CRF on tumor growth as a mediator of the response to stress in vivo.</p> <p>Methods</p> <p>For this purpose we used the 4T1 breast cancer cell line in cell culture and in vivo. Cells were treated with CRF in culture and gene specific arrays were performed to identify genes directly affected by CRF and involved in breast cancer cell growth. To assess the impact of peripheral CRF as a stress mediator in tumor growth, Balb/c mice were orthotopically injected with 4T1 cells in the mammary fat pad to induce breast tumors. Mice were subjected to repetitive immobilization stress as a model of chronic stress. To inhibit the action of CRF, the CRF antagonist antalarmin was injected intraperitoneally. Breast tissue samples were histologically analyzed and assessed for neoangiogenesis.</p> <p>Results</p> <p>Array analysis revealed among other genes that CRF induced the expression of SMAD2 and β-catenin, genes involved in breast cancer cell proliferation and cytoskeletal changes associated with metastasis. Cell transfection and luciferase assays confirmed the role of CRF in WNT- β-catenin signaling. CRF induced 4T1 cell proliferation and augmented the TGF-β action on proliferation confirming its impact on TGFβ/SMAD2 signaling. In addition, CRF promoted actin reorganization and cell migration, suggesting a direct tumor-promoting action. Chronic stress augmented tumor growth in 4T1 breast tumor bearing mice and peripheral administration of the CRF antagonist antalarmin suppressed this effect. Moreover, antalarmin suppressed neoangiogenesis in 4T1 tumors in vivo.</p> <p>Conclusion</p> <p>This is the first report demonstrating that peripheral CRF, at least in part, mediates the tumor-promoting effects of stress and implicates CRF in SMAD2 and β-catenin expression.</p

    An assessment of sputtered nitrogen-doped nickel oxide for all-oxide transparent optoelectronic applications: The case of hybrid NiO:N/TiO2 heterostructure

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    ransition metal oxides present a unique category of materials due to their versatile optical, electrical and mechanical properties. Nickel oxide (NiO) is an intrinsic p-type oxide semiconductor. P-NiO with controllable and reproducible physico-chemical properties, if combined with transparency and low temperature (low-T) fabrication processes, can be fully exploited in many transparent and/or flexible devices for applications, like energy management (production, manipulation, storage), sensing, wearable and health care electronics, etc. Reproducibility, transparency and low-T fabrication processes of p-type NiO are the motivation of this work. Nitrogen is one of the dopants used for modifying the properties of NiO. Until now, nitrogen-doped NiO, has shown inferior properties than those of pure NiO. In this work, we present nitrogen-doped NiO (NiO:N) thin films with enhanced properties compared to those of the undoped NiO. The NiO:N films were grown by sputtering on room-temperature substrates in plasma containing 50% Ar and 50% (O2+N2) gases. The undoped NiO film was oxygen-rich, single-phase cubic NiO, having transmittance less than 20%. Upon doping with nitrogen, the films became more transparent (around 65%), had a wide direct band gap (up to 3.67 eV) and showed clear evidence of indirect band gap, 2.50-2.72 eV, depending on %(O2-N2) in plasma. The changes in the properties of the films such as structural disorder, energy band gap, Urbach states and resistivity were correlated with the incorporation of nitrogen in their structure. The optimum NiO:N film was used to form a diode with spin-coated, mesoporous on top of a compact, TiO2 film. The hybrid NiO:N/TiO2 heterojunction was transparent showing good output characteristics, as deduced using both I-V and Cheung’s methods. The diode’s transparency and characteristics were further enhanced upon thermal treatment and this was attributed to improved NiO:N properties with annealing. Transparent NiO:N films can be realized for all-oxide flexible optoelectronic devices
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