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Distinctive Morphologies (distinctive + morphology)
Selected AbstractsDifferentiation trapping screen in live culture for genes expressed in cardiovascular lineagesDEVELOPMENTAL DYNAMICS, Issue 2 2004Weisheng V. Chen Abstract We have developed a gene trap vector that transduces an EGFP-neo fusion gene (Eno) to monitor the expression of trapped genes in living cells and embryos. Upon in vitro differentiation, most gene-trapped embryonic stem (ES) cell clones exhibited detectable green fluorescence in various specialized cell types, which can be followed in the live culture in real time. Populations of ES cell-derived cardiomyocytes, smooth muscle cells, vascular endothelial cells, and hematopoietic cells were readily recognized by their distinctive morphologies coupled with unique activities, allowing efficient screening for clones with trapped genes expressed in cardiovascular lineages. Applying G418 selection in parallel differentiation cultures further increased detection sensitivity and screening throughput by enriching reporter-expressing cells with intensified green fluorescent protein signals. Sequence analyses and chimera studies demonstrated that the expression of trapped genes in vivo closely correlated with the observed lineage specificity in vitro. This provides a strategy to identify and mutate genes expressed in lineages of interest for further functional studies. Developmental Dynamics 229:319,327, 2004. © 2004 Wiley-Liss, Inc. [source] Controllable Synthesis of Cu2O Microcrystals via a Complexant-Assisted Synthetic RouteEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 7 2010Wanqun Zhang Abstract A novel method using Cu(AC)2·H2O and dimethylglyoxime as reagents has been successfully developed for the controllable synthesis of Cu2O microcrystals with distinctive morphologies, including porous hollow microspheres, octahedral microcages, and microcrystals with truncated corners and edges and octahedral microcrystals. These structures can be fine-tuned by varying reaction temperature, reaction time, and concentration. The products were characterized by X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectra, and UV/Vis diffuse reflectance spectra. This is the first report of the preparation of the novel microcage structure of Cu2O through a simple solution-based route. By investigating the intermediate products which resemble the final crystal structures, a possible growth mechanism is proposed. Moreover, the investigations showed that the various 3D architectures of the as-made products exhibit different abilities to catalytically degrade rhodamine-B. Our work shows that octahedral Cu2O crystals with entirely {111} faces are photocatalytically more active than octahedral microcrystals with truncated corners and edges, suggesting the {111} faces of Cu2O nanostructures are catalytically more active than the {100} and {110} faces. Due to dual effect of the cavity structure and the {111} surfaces, the octahedral microcages with truncated corners and edges exhibit a higher extent of the photodecomposition reaction. As a result of very slow photocorrosion rate of the Cu2O microcrystal, it is expected that these microcrystals with different surfaces may find more applications in photocatalysis. [source] Undirected motility of filamentous cyanobacteria produces reticulate matsGEOBIOLOGY, Issue 3 2010R. N. SHEPARD The roles of biology in the morphogenesis of microbial mats and stromatolites remain enigmatic due to the vast array of physical and chemical influences on morphology. However, certain microbial behaviors produce complex morphological features that can be directly attributed to motility patterns. Specifically, laboratory experiments with a strain of the cyanobacteria Pseudanabaena demonstrate that distinctive morphologies arise from the undirected gliding and colliding of filaments. When filamentous cells collide, they align and clump, producing intersecting ridges surrounding areas with low cell density, i.e. reticulate structures. Cell motility is essential for the development of reticulates and associated structures: filaments organize into reticulates faster than cell division and growth, and conditions that inhibit motility also inhibit reticulate formation. Cell density of the inoculum affects the frequency of cell,cell collisions, and thus the time required for biofilm organization into reticulate structures. This also affects the specific geometry of the reticulates. These patterns are propagated into larger structures as cyanobacterial cell numbers increase and cells remain motile. Thus, cell motility is important for templating and maintaining the morphology of these microbial communities, demonstrating a direct link between a microbial behavior and a community morphology. Reticulate geometries have been identified in natural microbial mats as well as in the fossil record, and these structures can be attributed to the motility of filamentous bacteria. [source] Reactive blending of functionalized acrylic rubbers and epoxy resinsPOLYMER ENGINEERING & SCIENCE, Issue 9 2001C. Dispenza A high molecular weight acrylonitrile/butadiene/methacrylic acid (Nipol 1472) rubber is chosen to control processability and mechanical properties of a TGDDM (tetra glycidyl diphenyl methane) based epoxy resin formulation for aerospace composite applications. The physical blend of rubber and epoxy resin, achieved by dissolution of all the components in a common solvent, forms a heterogeneous system after solvent removal and presents coarse phase separation during cure that impairs any practical relevance of this material. A marked improvement of rubberepoxy miscibility is achieved by reactive blending (,pre-reaction') the epoxy oligomer with the functional groups present in the rubber. The epoxy-rubber ,adduct' so obtained appears as a homogeneous system at room temperature and also after compounding with the curing agent. Depending on the nature and extent of interactions developed between the rubber and the epoxy resin during ,pre-reaction,' materials with different resin flow characteristics, distinctive morphologies and mechanical properties after curing were obtained. The effect of ,pre-reaction' on the resin cure reaction kinetics has been also investigated. [source] Tetraethylenepentamine-Directed Controllable Synthesis of Wurtzite ZnSe Nanostructures with Tunable MorphologyCHEMISTRY - A EUROPEAN JOURNAL, Issue 31 2008Baojuan Xi Dr. Abstract A novel tetraethylenepentamine (TEPA)-directed method has been successfully developed for the controlled synthesis of ZnSe particles with distinctive morphologies, including nanobelts, nanowires, and hierarchically solid/hollow spheres. These structures, self-assembled from nanobelts and nanorods, have been synthesized by adjusting the reaction parameters, such as the solvent composition, reaction temperature, and the aging time. Results reveal that the volume ratio of H2O and TEPA plays a crucial role in the final morphology of ZnSe products. The mechanisms of phase formation and morphology control of ZnSe particles are proposed and discussed in detail. The products have been characterized by means of X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy (TEM), selected area electron diffraction, high-resolution TEM, Raman spectra and luminescence spectroscopy. The as-prepared ZnSe nanoparticles display shape- and size-dependent photoluminescent optical properties. This is the first time to report preparation of complex hollow structures of ZnSe crystals with hierarchy through a simple solution-based route. This synthetic route is designed to exploit a new H2O/TEPA/N2H4,H2O system possibly for the preparation of other semiconductor nanomaterials. [source] Spindle cell lipoma: an uncommon tumour with distinctive morphologyCYTOPATHOLOGY, Issue 2 2007S. K. Pathan No abstract is available for this article. [source] A fluorescently-labelled r-RNA targeted oligonucleotide probe for the in situ detection of G-bacteria of the genus Amaricoccus in activated sludgeJOURNAL OF APPLIED MICROBIOLOGY, Issue 5 2000A.-M. Maszenan A fluorescently-labelled r-RNAtargeted oligonucleotide probe specific for members of the genus Amaricoccus, which includes one group of the Gram-negative G-Bacteria seen in activated sludge systems, is described. These organisms, previously ,identified' on their distinctive morphology of cocci in tetrads, have been associated with poor performance of biological nutrient removal (EBNR) plants, by out-competing the polyphosphate accumulating bacteria. Methods of sample preparation for probing activated sludge are detailed, and preliminary surveys of 46 plants, using this probe, show that G-Bacteria belonging to the genus Amaricoccus are seen not only in large numbers in EBNR systems but also in conventional plants. The presence of single cells of this organism was common, emphasizing the dangers of relying on morphology and cell arrangement to identify these bacteria. [source] DESCRIPTION OF A NEW GENUS OF PFIESTERIA -LIKE DINOFLAGELLATE, LUCIELLA GEN.JOURNAL OF PHYCOLOGY, Issue 4 2007INCLUDING TWO NEW SPECIES: LUCIELLA MASANENSIS SP., NOV. (DINOPHYCEAE) A new genus of Pfiesteria -like heterotrophic dinoflagellate, Luciella gen. nov., and two new species, Luciella masanensis sp. nov. and Luciella atlantis sp. nov., are described. These species commonly occur with other small (<20 ,m) heterotrophic and mixotrophic dinoflagellates in estuaries from Florida to Maryland and the southern coast of Korea, suggesting a possible global distribution. An SEM analysis indicates that members of the genus Luciella have the enhanced Kofoidian plate formula of Po, cp, X, 4,, 2a, 6,, 6c, PC, 5+s, 5,, 0p, and 2,,. The two four-sided anterior intercalary plates are diamond shaped. The genus Luciella differs from the other genera in the Pfiesteriaceae by a least one plate in the plate tabulation and in the configuration of the two anterior intercalary plates. An SSU rDNA phylogenetic analysis confirmed the genus as monophyletic and distinct from the other genera in the Pfiesteriaceae. The morphology of Luciella masanensis closely resembles Pfiesteria piscicida Steid. et J. M. Burkh. and other Pfiesteria -like dinoflagellates in size and shape, making it easily misidentified using LM. Luciella atlantis, in contrast, has a more distinctive morphology. It can be distinguished from L. masanensis and other Pfiesteria -like organisms by a larger cell size, a more conical-shaped epitheca and hypotheca, larger rhombic-shaped intercalary plates, and an asymmetrical hypotheca. The genus Luciella is assigned to the order Peridiniales and the family Pfiesteriaceae based on plate tabulation, plate pattern, general morphology, and phylogenetic analysis. [source] Murine marrow-derived mesenchymal stem cell: isolation, in vitro expansion, and characterizationBRITISH JOURNAL OF HAEMATOLOGY, Issue 4 2003Lindolfo da Silva Meirelles Summary., In spite of the attention given to the study of mesenchymal stem cells (MSCs) derived from the bone marrow (BM) of humans and other species, there is a lack of information about murine MSCs. We describe the establishment of conditions for the in vitro expansion of plastic-adherent cells from murine BM for over 50 passages, and provide their characterization regarding morphology, surface marker profile and growth kinetics. These cells were shown to differentiate along osteogenic and adipogenic pathways, and to support the growth and differentiation of haematopoietic stem cells, and were thus operationally defined as murine mesenchymal stem cells (mMSCs). mMSCs were positive for the surface markers CD44, CD49e, CD29 and Sca-1, and exhibited a homogeneous, distinctive morphology. Their frequency in the BM of adult BALB/c and C57Bl/6 mice, normal or knockout for the , -L-iduronidase (IDUA) gene, was preliminarily estimated to be 1 per 11 300,27 000 nucleated cells. The emergence of a defined methodology for the culture of mMSCs, as well as a comprehensive understanding of their biology, will make the development of cellular and genetic therapy protocols in murine models possible, and provide new perspectives in the field of adult stem cells research. [source] | ||||||||||||||||