Au cours de la progression des cancers dorigine épithéliale, on observe une disparition des jonctions intercellulaires et une réorganisation de leurs composants. Par ailleurs, cette progression tumorale saccompagne également dune surexpression de certaines chimiokines par les cellules tumorales. Dans ce travail, nous nous sommes attachés à étudier la régulation potentielle de ces chimiokines par certaines molécules dadhérence. Nous avons plus particulièrement examiné linfluence de la caténine beta et de ZO-1 sur lexpression des chimiokines étant donné leur particularité de pouvoir effectuer la navette entre la membrane et le noyau et leur implication dans des voies de signalisation. Dans un premier chapitre de résultats (chapitre III.1.1), nous rapportons notre étude concernant la régulation de MCP-1/CCL2 par la voie de signalisation caténine beta Publication 1 Nos travaux détaillant la régulation de lIL-8/CXCL8 par ZO-1 font lobjet dun second chapitre de résultats (chapitre III.1.2) Publication 2 Parallèlement à notre axe principal de recherche centré sur la régulation de lexpression des chimiokines, nous avons également participé à des travaux montrant linfluence de la voie de signalisation caténine beta sur la régulation de la vimentine lors de la transition épithélio-mésenchymateuse (TEM) associée à la progression tumorale. Un troisième chapitre de résultats est consacré à lexposé de ces travaux (chapitre III.2). Publications 3, 4, 5

The aim of this master thesis was to compare EELS in TEM with TEM-EDS and WDS-EPMA for quantitative analysis of γ-phase in cemented carbide. Especially, the quantification of the light elements nitrogen and carbon in compounds like TiCxN1-x is interesting, since this is problematic. The techniques were compared by acquiring spectra for quantification of two samples of cemented carbide containing γ-phase (Tix,W1-x)(CyN1-y) with different nitrogen and tungsten content. Also, a rigorous evaluation about how EELS spectra best is acquired and processed was performed in order to enable the comparison. Experimental results show that EELS gives satisfying results for TiC0.7N0.3 and that EELS is comparable with WDS-EPMA for quantification of nitrogen, carbon and titanium in (Tix,W1-x)(CyN1-y) when the atomic concentration of nitrogen is around 20%. However, EELS was not used for quantification of tungsten. Concluded is also that EELS and WDS should be considered as complementary rather than competing techniques.

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A nanofilm rotation method is developed to study the rotation of nanograins and the formation of various low energy interfaces. Epitaxial (100), (110), (111) and (112) NiO nanofilms are prepared by ion beam sputtering onto the (100), (110), (111) and (112) surfaces of NaCl single crystal. By overlapping of the above films with an angle difference, and annealing at relatively low temperatures 100 ¢Jthe nanograins are induced to rotate till a metastable interface is reached. The rotation process and the metastable interfaces are determined by transmission electron microscopy. Many new interfaces between mixed planes are found, and their orientation relationships and structures are analyzed. The study discovered eight groups of metastable orientation relations, respectively, which have not been reported in literatures. 2¡¦ orientation relationship is [11 ]( 10)//[01 ]( 11) 2¡¦¡¦ orientation relationship is [00 ]( 10)//[ 0 ]( 11) 4e1 orientation relationship is [13 ]( 12)//[110](00 1) 4¡¦ orientation relationship is [1 1]( 12)//[0 0](00 1) 4e2 orientation relationship is [13 ]( 12)//[100](00 1) 5¡¦ orientation relationship is [ 1 ]( 12)// [01 ] ( 11) 6¡¨ orientation relationship is [110]( 12)// [001] ( 10) 6¡¦¡¦¡¦ orientation relationship is [110]( 12)// [ 1] ( 10)

Ti thin films were deposited by a radio frequency ion-beam sputtering system. Deposition resulted from sputtering a Ti target (99.995%) with an Ar ion beam. Epitaxial TiO thin films with different orientations, which came from oxidizing Ti thin films, were prepared on single-crystal NaCl substrate. The formation of epitaxial TiO2 thin films (anatase or rutile phase) by oxidation of epitaxial TiO thin films was investigated. The composition, microstructure, and orientation relationships between interfaces were analyzed by TEM and Fourier transformation in the present report. Epitaxial TiO thin films with different orientations were prepared on single-crystal NaCl substrate in the present study. The formation of epitaxial TiO2 thin films (anatase or rutile) by oxidation of epitaxial TiO thin films, which were first grown on different NaCl surfaces, was investigated. The composition, microstructure, and orientation relationships between interfaces were analyzed by TEM and Fourier transformation in this report. The TiO to anatase phase transformation has been studied by transmission electron microscopy in this Article. It is shown that prior formation of TiO from Ti film can induce the formation of anatase by thermal oxidation in air, otherwise only rutile is formed. Ti film deposited on the NaCl (001) surface is induced to form epitaxial TiO film by thermal oxidation in air. Further thermal oxidation in air partially transformed TiO into anatase (A) with a parallel orientation relationship of {200}A // {200}TiO. Detailed analysis of the lattice fringes image of the specimen reveals the presence of very high density of misfit dislocations. The TiO to anatase transformation is reversible as further annealing in a vacuum can turn the anatase back into TiO and eliminates the misfit dislocations. The transformation is analyzed in terms of the crystal structure, orientation relationship, and the dislocation distribution, which show that the TiO to anatase transformation is due to the close similarity between their structures. (Chapter 1) The anatase TiO2 (001) surface was shown to have superior photoreactivity. Epitaxial anatase (001) films used to be grown on single-crystal SrTiO3 and LaAlO3 substrates. It is shown in this report that these films can be grown also on the NaCl substrate, which is much cheaper and easily prepared. Epitaxial TiO (001) films were first grown on the NaCl (001) substrate. By testing the TiO-to-anatase transformation over temperature and time ranges, an epitaxial anatase (001) film was prepared by simple thermal oxidation in air. The formation of a single-variant anatase (001) film instead of a multiple-variant film is discussed in this report. (Chapter 2) An epitaxial rutile (100) thin film has been grown on NaCl substrate instead of other more expensive substrates. An epitaxial TiO (111) thin film with minor Ti phase was first deposited on the NaCl (111) surface by thermal evaporation. It was then transformed into the epitaxial rutile (100) thin film by subsequent thermal oxidation in air. TEM was used to analyze the phases and the orientation relationship. Our previous result showed that an epitaxial anatase (001) film was formed on the NaCl (001) surface in a similar process. The substrate-dependent formation of different TiO2 phase is also discussed in terms of the mismatch of the interfaces. (Chapter 3)

Nanoporous polymer hydrogels offer a desirable combination of mechanical, optical, and transport characteristics that have placed them at the core of a variety of biomedical technologies including engineered tissue scaffolds, substrates for controlled release of pharmaceutical compounds, and sieving matrices for electrophoretic separation of DNA and proteins. Ultimately, we would like to obtain a detailed picture of the nanoscale pore morphology and understand how it can be manipulated so that we can rationally identify gel formulations best suited for a specific application. But this goal has proven elusive because the most fundamental descriptors of the pore network architecture (e.g., the average pore size and its polydispersity) are particularly difficult to measure in polymer hydrogels. Here we introduce an approach that enables both the mean pore size and the pore size distribution to be quantitatively determined without prior knowledge of any physical material parameters A novel technique to prepare TEM samples was developed so that the nanoscale hydrogel pore size, pore shape and distribution are clearly visualized and quantitatively studied for the first time. The pore sizes of the hydrogel are also estimated with rheology. A new fixture is used in the rheometer and the whole polymerization process can be directly studied using an in-situ rheology experiment. A series of thermoporometry experiments are also conducted, and suitable methods and equations to study hydrogel pore size and distribution are chosen. The pore size derived from TEM, rheology, DSC is compared and their values are self-consistent. These techniques help us understand how the nanoporous morphology of crosslinked polyacrylamide hydrogels is influenced by their chemical composition and polymerization conditions. It is interesting to find hydrogels with similar pore size but different distribution. For two hydrogels with similar pore size, the broader the distribution, the faster the release rate and the higher the accumulated release percentage. So we can control the release of trapped molecules by simply varying the hydrogel pore size distribution. This discovery would have a very promising potential in the application of pharmaceuticals.

In this paper, we use a room temperature processing system, Liquid Phase Deposition(LPD) method, to grow silicon dioxide. The advantages are cheap equipment, low temperature growth, and no thermal stress. The quality is good enough to be used in IC devices. To inverstigate the properties of silicon Dioxide, we have done different physical and chemical test, including AES,TEM,FTIR,P-etch rate. We used the high frequency C-V curve to study the interface properties. The leakage current help to clarify the film quality. Moreover, we also discuss the growth mechanism in order to more understanding of LPD method.

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Abstract This study focused on the structure of the particles developed in the PMMA matrix as a function of (a) coupling agent (£^-MPS) and (b) TEOS content. We investigated the difference of using TEOS monomer directly added to silica particles. The polymer precursors are catalyzed using acidic catalysts and undergo the sol-gel reaction to form a hybrid sol-gel material. This composite shows that highly optical transparency and microphase separation at the molecular level. The characteristics and properties of the polymer precursors and their hybrid materials were characterized by Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimogravimetic analysis (TGA). As for the influence of chemistry structure on morphology and thermal properties, experimental evidence form observations by scanning electron microscopy (SEM), mulitpoints analysis, and transmission electron microscopy (TEM). TEM was used to study the phase separation as well as the fractal structure of these particles present in the system. According to some result, it was found the compatibility between PMMA and silica mainly comes form incorporating the polymer with silica chemical bonding. This chemical bonding not only restrains silyl ester groups form hydrolyzing but also reduces silanol aggregation. Moreover, the thermal properties of the organic¡Vinorganic hybrid are improved as silica content increases.

Nanoparticles possess unique physical, chemical, optical and electronic properties stemming from their nanoscale dimensions and are currently used in catalysis, microelectronics, drug delivery, as well as other applications. However, due to their large surface area-to-volume ratio, nanoparticles have a strong tendency to coalesce and sinter during processing or usage over short time scales and at low temperatures, which lead to significant changes in behavior and performance. In this work, in-situ transmission electron microscopy (TEM) heating has been used to investigate the effects of particle size, temperature and carbon capping layers on sintering in face-centered cubic (FCC) metallic nanoparticles. For the first time, we make direct and real-time measurements of nanoparticle size, neck growth, dihedral angle and grain boundary motion during sintering, which are then used to calculate fundamental material transport parameters such as surface diffusivity and grain boundary mobility. We observe that carbon surface coatings typically present on most commercial nanoparticles can significantly inhibit sintering in nanoparticles. Also, a new mechanism for coalescence in nanoparticles is shown where small clusters on the support can initiate neck growth by forming a bridge between the nanoparticles consisting of individual atoms or small clusters of atoms. In-situ TEM experiments provide critical and valuable real-time dynamic information for direct investigation of the link between the evolution of sintering and controlling mechanisms, which conventional experiments such as post-mortem TEM observations are not capable of conveying. / text