166 research outputs found

    Optical Absorption and Raman Spectroscopy Study of the Fluorinated Double-Wall Carbon Nanotubes

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    Double-wall carbon nanotube (DWNT) samples have been fluorinated at room temperature with varied concentration of a fluorinating agent BrF3. Content of the products estimated from X-ray photoelectron data was equal to CF0.20 and CF0.29 in the case of deficit and excess of BrF3. Raman spectroscopy showed considerable decrease of carbon nanotube amount in the fluorinated samples. Analysis of optical absorption spectra measured for pristine and fluorinated DWNT samples revealed a selectivity of carbon nanotube fluorination. Nanotubes with large chiral angle are more inert to the fluorinating agent used

    AFM imaging of functionalized carbon nanotubes on biological membranes

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    Multifunctional carbon nanotubes are promising for biomedical applications as their nano-size, together with their physical stability, gives access into the cell and various cellular compartments including the nucleus. However, the direct and label-free detection of carbon nanotube uptake into cells is a challenging task. The atomic force microscope (AFM) is capable of resolving details of cellular surfaces at the nanometer scale and thus allows following of the docking of carbon nanotubes to biological membranes. Here we present topographical AFM images of non-covalently functionalized single walled (SWNT) and double walled carbon nanotubes (DWNT) immobilized on different biological membranes, such as plasma membranes and nuclear envelopes, as well as on a monolayer of avidin molecules. We were able to visualize DWNT on the nuclear membrane while at the same time resolving individual nuclear pore complexes. Furthermore, we succeeded in localizing individual SWNT at the border of incubated cells and in identifying bundles of DWNT on cell surfaces by AFM imaging

    Quantum Zakharov Model in a Bounded Domain

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    We consider an initial boundary value problem for a quantum version of the Zakharov system arising in plasma physics. We prove the global well-posedness of this problem in some Sobolev type classes and study properties of solutions. This result confirms the conclusion recently made in physical literature concerning the absence of collapse in the quantum Langmuir waves. In the dissipative case the existence of a finite dimensional global attractor is established and regularity properties of this attractor are studied. For this we use the recently developed method of quasi-stability estimates. In the case when external loads are C∞C^\infty functions we show that every trajectory from the attractor is C∞C^\infty both in time and spatial variables. This can be interpret as the absence of sharp coherent structures in the limiting dynamics.Comment: 27 page

    Effect of Palmitic Acid on the Electrical Conductivity of Carbon Nanotubes−Epoxy Resin Composites

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    We found that the palmitic acid allows an efficient dispersion of carbon nanotubes in the epoxy matrix. We have set up an experimental protocol in order to enhance the CNTs dispersion in epoxy resin. Electrical conductivity is optimal using a 1:1 CNTs to palmitic acid weight ratio. The associated percolation threshold is found between 0.05 and 0.1 wt % CNTs, i.e., between 0.03 and 0.06 vol %. The SEM image shows essentially individual CNTs which is inagreement with conductivity measurements. In comparison with composites without palmitic acid, the use of palmitic acid improves the electrical properties of CNTs-epoxy resin composites

    Fe-substituted mullite powders for the in situ synthesis of carbon nanotubes by catalytic chemical vapor deposition

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    Powders of iron-substituted mullite were prepared by combustion and further calcination in air at different temperatures. A detailed study involving notably Mošssbauer spectroscopy showed that the Fe3+ ions are distributed between the mullite phase and a corundum phase that progressively dissolves into mullite upon the increase in calcination temperature. Carbon nanotube-Fe-mullite nanocomposites were prepared for the first time by a direct method involving a reduction of these powders in H2-CH4 and without any mechanical mixing step. The carbon nanotubes formed by the catalytic decomposition of CH4 on the smallest metal particles are mostly double-walled and multiwalled, although some carbon nanofibers are also observed

    Wild-type ALK and activating ALK-R1275Q and ALK-F1174L mutations upregulate Myc and initiate tumor formation in murine neural crest progenitor cells.

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    The anaplastic lymphoma kinase (ALK) gene is overexpressed, mutated or amplified in most neuroblastoma (NB), a pediatric neural crest-derived embryonal tumor. The two most frequent mutations, ALK-F1174L and ALK-R1275Q, contribute to NB tumorigenesis in mouse models, and cooperate with MYCN in the oncogenic process. However, the precise role of activating ALK mutations or ALK-wt overexpression in NB tumor initiation needs further clarification. Human ALK-wt, ALK-F1174L, or ALK-R1275Q were stably expressed in murine neural crest progenitor cells (NCPC), MONC-1 or JoMa1, immortalized with v-Myc or Tamoxifen-inducible Myc-ERT, respectively. While orthotopic implantations of MONC-1 parental cells in nude mice generated various tumor types, such as NB, osteo/chondrosarcoma, and undifferentiated tumors, due to v-Myc oncogenic activity, MONC-1-ALK-F1174L cells only produced undifferentiated tumors. Furthermore, our data represent the first demonstration of ALK-wt transforming capacity, as ALK-wt expression in JoMa1 cells, likewise ALK-F1174L, or ALK-R1275Q, in absence of exogenous Myc-ERT activity, was sufficient to induce the formation of aggressive and undifferentiated neural crest cell-derived tumors, but not to drive NB development. Interestingly, JoMa1-ALK tumors and their derived cell lines upregulated Myc endogenous expression, resulting from ALK activation, and both ALK and Myc activities were necessary to confer tumorigenic properties on tumor-derived JoMa1 cells in vitro

    Arnica montana : évaluation des ressources génétiques françaises en vue du développement de la culture en plaine et en montagne

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    Ce volume regroupe les textes issus du programme Casdar "Innovation et Partenariat" et "Recherche finalisĂ©e et innovation" de 2013. Le colloque de restitution s’est dĂ©roulĂ© le 6 fĂ©vrier 2019 sous l’égide du GIS Relance AgronomiqueArnica montana is a major medicinal specie, which is now mainly produced from wild harvesting,especially in mainland France. As the wild resource is decreasing, and in order to maintain or even Gourlin L. et al. 68 Innovations Agronomiques 71 (2019), 67-80 develop the French production, cultivation is a good option, that is still very limited, because of its difficulty. Finding the right plant material could help to enhance cultivation programs. This project aimed at growing 24 wild populations, which were collected in mainland France, and to compare them with 2 commercial varieties, ‘Arbo’ and ‘Arnimed’. This was set on 4 experimentation spots, chosen for their potential match for Arnica cultivation. The experiment lasted 3 years, and morphological andagronomical subjects were studied on the populations. Sesquiterpene lactones and flavonoidsanalyzed, and a new methodology of evaluation was developed. The results showed extreme variabilityof phenotypic and chemical expression of the different populations. An important death rate has beennoticed on wild populations, but the causes are still unknown. On the set of variables chosen,commercial varieties ‘Arbo’ and ‘Arnimed’ were particularly competitive, and two wild populations standout with promising results. One seems appropriate for starting selection works on a variety that would besuitable for loaw altitude, and the other one could be a local (French) alternative to the cultivation ofselected varieties (‘Arbo’ and ‘Arnimed’ are from Swiss and German selection work).L’arnica des montagnes est une espĂšce mĂ©dicinale importante dont la production est principalementissue de la cueillette Ă  l’état sauvage, notamment sur le territoire mĂ©tropolitain. La ressource Ă©tant enrĂ©gression, le maintien, voire le dĂ©veloppement de la production française passe donc par la mise enculture, actuellement anecdotique car difficile. Certains freins pourraient ĂȘtre levĂ©s par la mise enĂ©vidence de matĂ©riel vĂ©gĂ©tal adaptĂ© Ă  la production. L’objectif de ce projet Ă©tait de mettre en culture 24populations d’origines sauvages (prospectĂ©es en France mĂ©tropolitaine) et de les comparer Ă  deuxvariĂ©tĂ©s commerciales tĂ©moins ‘Arbo’ et ‘Arnimed’, sur 4 sites d’expĂ©rimentation aux contextespĂ©doclimatiques variĂ©s mais a priori adaptĂ©s Ă  la culture de l’espĂšce. Durant les 3 annĂ©es d’essai, unsuivi morphologique et agronomique des populations a Ă©tĂ© rĂ©alisĂ©. Des analyses des sesquiterpĂšneslactones et flavonoĂŻdes ont Ă©tĂ© effectuĂ©es, et une nouvelle mĂ©thodologie de dosage de ces composĂ©s aĂ©tĂ© dĂ©veloppĂ©e. Les rĂ©sultats mettent en exergue la forte variabilitĂ© de l’expression phĂ©notypique etchimique des diffĂ©rentes souches testĂ©es. Une forte mortalitĂ© globale a pu ĂȘtre constatĂ©e surl’ensemble des populations sauvages Ă©tudiĂ©es sans que les causes aient pu en ĂȘtre identifiĂ©es. Surl’ensemble des variables suivies, les variĂ©tĂ©s commerciales ‘Arbo’ et ‘Arnimed’ sont particuliĂšrementperformantes, et deux populations sauvages se dĂ©marquent par leurs rĂ©sultats intĂ©ressants : l’uneparait pertinente pour dĂ©marrer des travaux de sĂ©lection d’une variĂ©tĂ© adaptĂ©e Ă  la basse altitude,tandis que l’autre, originaire du Massif central, pourrait se proposer comme une alternative d’originelocale (française) Ă  la culture de variĂ©tĂ©s commerciales sĂ©lectionnĂ©es (suisse et allemande)

    The Chemokine Receptor CXCR4 Strongly Promotes Neuroblastoma Primary Tumour and Metastatic Growth, but not Invasion

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    Neuroblastoma (NB) is a heterogeneous, and particularly malignant childhood neoplasm in its higher stages, with a propensity to form metastasis in selected organs, in particular liver and bone marrow, and for which there is still no efficient treatment available beyond surgery. Recent evidence indicates that the CXCR4/CXCL12 chemokine/receptor axis may be involved in promoting NB invasion and metastasis. In this study, we explored the potential role of CXCR4 in the malignant behaviour of NB, using a combination of in vitro functional analyses and in vivo growth and metastasis assessment in an orthotopic NB mouse model. We show here that CXCR4 overexpression in non-metastatic CXCR4-negative NB cells IGR-NB8 and in moderately metastatic, CXCR4 expressing NB cells IGR-N91, strongly increased tumour growth of primary tumours and liver metastases, without altering the frequency or the pattern of metastasis. Moreover shRNA-mediated knock-down experiments confirmed our observations by showing that silencing CXCR4 in NB cells impairs in vitro and almost abrogates in vivo growth. High levels of CXCL12 were detected in the mouse adrenal gland (the primary tumour site), and in the liver suggesting a paracrine effect of host-derived CXCL12 on NB growth. In conclusion, this study reveals a yet unreported NB-specific predominant growth and survival-promoting role of CXCR4, which warrants a critical reconsideration of the role of CXCR4 in the malignant behaviour of NB and other cancers

    Cancer stem-like cells from head and neck cancers are chemosensitized by the Wnt antagonist, sFRP4, by inducing apoptosis, decreasing stemness, drug resistance and epithelial to mesenchymal transition

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    Cancer stem cells (CSCs) of head and neck squamous cell carcinoma (HNSCC) are defined by high self-renewal and drug refractory potential. Involvement of Wnt/ß-catenin signaling has been implicated in rapidly cycling cells such as CSCs, and inhibition of the Wnt/ß-catenin pathway is a novel approach to target CSCs from HNSCC. In this study, we found that an antagonist of FrzB/Wnt, the secreted frizzled-related protein 4 (sFRP4), inhibited the growth of CSCs from two HNSCC cell lines, Hep2 and KB. We enriched the CD44+ CSC population, and grew them in spheroid cultures. sFRP4 decreased the proliferation and increased the sensitivity of spheroids to a commonly used drug in HNSCC, namely cisplatin. Self-renewal in sphere formation assays decreased upon sFRP4 treatment, and the effect was reverted by the addition of Wnt3a. sFRP4 treatment of spheroids also decreased ß-catenin, confirming its action through the Wnt/ß-catenin signaling pathway. Quantitative PCR demonstrated a clear decrease of the stemness markers CD44 and ALDH, and an increase in CD24 and drug-resistance markers ABCG2 and ABCC4. Furthermore, we found that after sFRP4 treatment, there was a reversal in the expression of epithelial to mesenchymal (EMT) markers with the restoration of the epithelial marker E-cadherin, and depletion of EMT-specific markers twist, snail and N-cadherin. This is the first report demonstrating that the naturally occurring Wnt inhibitor, sFRP4, can be a potential drug to destroy CSC-enriched spheroids from HNSCCs. The repression of EMT and the decrease in stemness profile further strengthen the use of sFRP4 as a potent therapeutic against CSC
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