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Larger Cells (larger + cell)
Selected AbstractsTemperature-induced plasticity at cellular and organismal levels in the lizard Anolis carolinensisINTEGRATIVE ZOOLOGY (ELECTRONIC), Issue 3 2010Rachel M. GOODMAN Abstract Among ectotherms, individuals raised in cooler temperatures often have larger body size and/or larger cell size. The current study tested whether geographic variation in cell size and plasticity for cell size exist in a terrestrial, ectothermic vertebrate, Anolis carolinensis Voigt, 1832. We demonstrated temperature-induced plasticity in erythrocytes and epithelial cells of hatchlings lizards derived from the eggs of females sampled from four populations and incubated at multiple temperatures. Larger cells were produced in hatchlings from cooler treatments; however, hatchling body size was unaffected by temperature. Therefore, temperature-induced plasticity applies at the cellular, but not organismal, level in A. carolinensis. In addition, reaction norms for cell size differed among populations. There was a latitudinal trend in cell size and in plasticity of cell size among our study populations. The two southernmost populations showed plasticity in cell size, whereas the two northernmost ones did not. We suggest that selection pressure for larger cell size in northern, cooler environments has restricted plasticity in A. carolinensis applied at the cellular level in response to variable incubation environments. [source] Characteristics of okadaic acid,induced cytotoxic effects in CHO K1 cellsENVIRONMENTAL TOXICOLOGY, Issue 6 2003C. Huynh-Delerme Abstract This article reports the results of investigations into the process of cell death induced in the Chinese hamster ovary cell K1 subclone (CHO K1) by okadaic acid (OA), a hydrophobic polyether produced by marine dinoflagellates. The IC50 was about 13 nM OA after 24 h of treatment, as determined using neutral red. With the MTT assay, the IC50 was 25 nM, although in this case 25% of the initial staining was still observed at 100 nM. Hoechst staining showed that mitotic figures accumulated at 12 nM OA after a 24- or 48-h treatment. In experiments limited to a 3-day treatment without changing the medium, CHO K1 cells were engaged in the death process at 50 nM OA after about 20 h and at 10 nM OA after 48 h. In many cells nuclear fragmentation that resulted in the apparent appearance of vesicles correlated with increasing cellular volume. But additional cell fragmentation was not observed with any treatment, and the chromatin material seemed to progressively disappear inside the cells. DNA fragmentation was analyzed by electrophoresis and with the TUNEL technique. With both techniques, the DNA was fragmented by 48 h in both 25 and 50 nM OA. Electrophoresis showed that both adherent and nonadherent cells were affected. Annexin-positive/ propidium iodide (PI),negative cells were rarely observed after OA treatment. Some were seen under the scanning cytometer after 20 h at 50 nM OA or after 48 h at 10 nM OA, but they were never detected by flow cytometry. Most of the time scanning cytometry showed either unstained cells or PI-positive (annexin-positive or -negative) cells (48 h, 50 nM, or 72 h, 10 nM). Flow cytometry cytograms showed two cell subpopulations: one composed of a majority of smaller cells, the other of larger cells. The larger cells markedly decreased with time and OA treatment (50 and 100 nM). Stained-cell counting showed that all cells that stained were both annexin- and PI positive and that most PI-positive cells were smaller. Ki67 antigen labeling showed the proliferative activity of CHO K1 cultures but also demonstrated the loss of this activity in smaller cells treated with 50 nM OA for 48 h. We concluded that in our culture conditions the main OA target within CHO K1 cultures was dividing cells. Our results suggest that cells with disturbed metaphase,anaphase enter apoptosis, leading to necrotic daughter cells. © 2003 Wiley Periodicals, Inc. Environ Toxicol 18: 383,394, 2003 [source] Differentiation of human ameloblast-lineage cells in vitroEUROPEAN JOURNAL OF ORAL SCIENCES, Issue 2006Qiaomei Yan Previous studies have shown that ameloblast-like cells can be selectively cultured from the enamel organ in a serum-free medium with low calcium concentrations. The purpose of this study was to further characterize this culture system to identify differentiated ameloblast-lineage cells. Tooth organs from 19,24-wk-old fetal cadavers were either frozen and cryosectioned for immunostaining, or digested in collagenase/dispase for cell culture. The cells were grown in keratinocyte media supplemented with 0.05 mM calcium, and characterized by morphology and immunofluorescence. Epithelial clones with two distinct morphologies, including smaller cobblestone-shaped cells and larger (5,15 times in size) rounded cells, began to form between day 8 and day 12 after culture. The cobblestone-shaped cells continued to proliferate in culture, while the larger cells proliferated slowly or not at all. These larger cells formed filopodia, usually had two or more nuclei and a radiating cytoplasm at the cell margin, and were more abundant with increasing time in culture. Both cell types stained for cytokeratin 14, and the larger cells appeared more differentiated, showing stronger staining for amelogenin and ameloblastin. Immunofluorescence of the tooth bud sections showed staining for these matrix proteins as ameloblasts differentiated from the inner enamel epithelium. These results show the successful culture of differentiating ameloblast-lineage cells, and lay a foundation for use of these cells to further understand ameloblast biology with application to tooth enamel tissue engineering. [source] Compressive response and energy absorption of foam EPDMJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Biqin Wang Abstract Ethylene,propylene,diene terpolymer foam was prepared by two different processing routes. The microstructure and mechanical properties of the foams with wide relative density ranging from 0.11 to 0.62 have been studied via scanning electron microscopy and mechanical testing, respectively. Scanning electron microscopy shows that the foam with lower relative density has a unique bimodal cell size structure, which the larger cells inlay among the smaller cells, while the foam articles with higher relative density have thicker cell walls with few small cells. The compressive stress,strain curves show that the foam articles with lower relative density have three regimes: linear elastic, a wide slightly rising plateau, and densification, while the foam articles with higher relative density have only two regimes: the longer linear elastic and densification. The relative modulus increases with the increase in the relative density. The contribution of the gas trapped in the cell to the modulus could be neglected. The energy absorbed per unit volume is relationship with the permitted stress and the relative density. The efficiency and the ideality parameter were evaluated from the compressive stress,strain plots. The parameters were plotted against stress to obtain maximum efficiency and the maximum ideality region, which can be used for optimizing the choice for practical applications in cushioning and packaging. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] The effect of cell size distribution during the cooling stage of cryopreservation without CPAAICHE JOURNAL, Issue 8 2010S. Fadda Abstract A novel model capable of quantitatively describing and predicting intracellular ice formation (IIF) as a function of temperature in a cell population characterized by a size distribution is proposed. The model overcomes the classical approach which takes into account a population of identically sized cells. The size distribution dynamics of a cell population in response to water osmosis and IIF occurrence during the cooling stage of a standard cryopreservation protocol without using cryoprotective agent (CPA) is simulated by means of a suitable population balance approach. Specifically, the model couples the classical water transport equation developed by Mazur1 to the quantitative description of nucleation and diffusion-limited growth of ice crystals in the framework of a 1-D population balance equation (PBE). It is found that IIF temperature depends on the cell size, i.e., it is higher for larger cells. Correspondingly, the probability of IIF (PIIF) results to be dependent on the initial size distribution of the cell population. Model's parameters related to the osmotic behavior of the cell population and to IIF kinetics are obtained by comparison between theoretical results and suitable experimental data of isolated rat hepatocytes available in the literature. Model reliability is successfully verified by predicting the experimental data of PIIF at different, constant cooling rates with better accuracy as compared to the theoretical approaches available in the literature. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source] Morphological spectrum of cyclin D1-positive mantle cell lymphoma: Study of 168 casesPATHOLOGY INTERNATIONAL, Issue 10 2001Yasushi Yatabe Immunostaining for cyclin D1 is essential for reliable diagnosis of mantle cell lymphoma (MCL). However, a small number of cyclin D1-positive lymphomas other than MCL have been encountered. Our goal was to investigate the morphological spectrum of MCL as a disease entity, based on cyclin D1 overexpression. We reviewed 181 biopsy specimens obtained from 168 cases of cyclin D1-positive MCL. Typical findings were the presence of nodular (53.9% of cases) or diffuse (46.1%) histological patterns, containing mantle zone patterns (16.8%), naked germinal centers (33.5%) and perivascular hyaline deposition (83.2%). Unusual findings of residual germinal centers with a mantle cuff (four cases) and follicular colonization (two cases) were seen. High magnification showed a monotonous proliferation of tumor cells with cytological diversity including small (3.0%), intermediate (43.1%), medium (34.1%), medium, large (13.2%) and large (6.6%) cells. Pleomorphic and blastic / blastoid variants were encountered in 9.6 and 7.2% of cases, respectively. Three cases had foci of cells of considerable size, with a moderately abundant pale cytoplasm resembling marginal zone B cells. Two cases showed an admixture of cells which appeared transformed and mimicked the histology of chronic lymphocytic leukemia / small lymphocytic leukemia. In one, neoplastic mantle zones were surrounded by sheets of mature plasma cells, resembling the plasma cell type of Castleman's disease. An admixture of areas characteristic of MCL and of other larger cells, indicating histological progression or a composite lymphoma, were observed in seven cases. In high-grade lesions of five cases, nuclear staining of cyclin D1 was rarely detected. In our experience, cyclin D1 expression was also found in nine lymphomas other than MCL (five plasma cell myelomas, three Hodgkin's disease and one anaplastic large cell lymphoma). The application of cyclin D1 staining prompted us to recognize the broad morphological spectrum of MCL. MCL can be diagnosed with the application of cyclin D1 immunostaining, if careful attention is given to architectural and cytological features. [source] Intestinal Villus Histological Alterations in Piglets fed Dietary Charcoal Powder Including Wood Vinegar Compound LiquidANATOMIA, HISTOLOGIA, EMBRYOLOGIA, Issue 1 2004A. Mekbungwan Summary To investigate the effects of dietary charcoal powder including wood vinegar compound liquid (CWVC, 4 : 1) on intestinal villus histology, piglets were fed 0, 1, 3 and 5% dietary CWVC diets for 30 days. Feed intake and body weight gain were measured during the experimental period. At the end of the experiments, intestinal villus height, epithelial cell area and cell mitosis were examined using light microscopy (LM), and the duodenal villus tip surface was observed using scanning electron microscopy (SEM). Feed efficiency tended to be improved in the CWVC group. The 3% CWVC group showed the highest value, followed by 1% CWVC group of most LM parameters in most intestinal parts, but the 5% CWVC group showed the almost similar value compared with the control. In addition, on the duodenal villus tip surface, the 3% CWVC group showed a clearer cell outline, larger cells and cells protuberated further into the lumen than those of the 1% CWVC group. However, the 5% CWVC group showed faint SEM features than the 1% CWVC group. The present trend of improved feed efficiency after feedings of dietary CWVC demonstrates that the CWVC could be incorporated into piglet diets up to 3% level, and that the CWVC might activate intestinal functions both at villus and cellular levels. [source] Regional specialization of the Ganglion cell density in the retina of the Ostrich (Struthio camelus)ANIMAL SCIENCE JOURNAL, Issue 1 2010Mohammad L. RAHMAN ABSTRACT In this study, retinal whole-mount specimens were prepared and stained with 0.1% cresyl violet for the ganglion cell study in the Ostrich (Struthio camelus). The total number, distribution, and size of these cells were determined in different retinal regions. The mean total number of ganglion cells (three retinas) was 1 435 052 with an average density of 652 cells/mm2. The temporo , nasal area of the retina with high cell density were identified with the peak of 7525 cells/mm2 in the central area. The size of most ganglion cells ranged from 113,403 µm2, with smaller cells predominating along the temporo-nasal streak above the optic disc and larger cells comprising more of the peripheral regions. The average thickness of the retina was 196 µm. The central area was the thickest area (268.6 µm), whereas the peripheral area was the thinnest area. Thus, the specialization of ganglion cell densities, their sizes and the thickness of the retina support the notion that the conduction of visual information towards the brain from all regions of the retina is not uniform, and suggests that the temporo , nasal streak is the fine quality area for vision in ostriches. [source] Ecological correlates of body size in relation to cell size and cell number: patterns in flies, fish, fruits and foliageBIOLOGICAL REVIEWS, Issue 2 2007Jeff Arendt Abstract Body size is important to most aspects of biology and is also one of the most labile traits. Despite its importance we know remarkably little about the proximate (developmental) factors that determine body size under different circumstances. Here, I review what is known about how cell size and number contribute to phenetic and genetic variation in body size in Drosophila melanogaster, several fish, and fruits and leaves of some angiosperms. Variation in resources influences size primarily through changes in cell number while temperature acts through cell size. The difference in cellular mechanism may also explain the differences in growth trajectories resulting from food and temperature manipulations. There is, however, a poorly recognized interaction between food and temperature effects that needs further study. In addition, flies show a sexual dimorphism in temperature effects with the larger sex responding by changes in cell size and the smaller sex showing changes in both cell size and number. Leaf size is more variable than other organs, but there appears to be a consistent difference between how shade-tolerant and shade-intolerant species respond to light level. The former have larger leaves via cell size under shade, the latter via cell number in light conditions. Genetic differences, primarily from comparisons of D. melanogaster, show similar variation. Direct selection on body size alters cell number only, while temperature selection results in increased cell size and decreased cell number. Population comparisons along latitudinal clines show that larger flies have both larger cells and more cells. Use of these proximate patterns can give clues as to how selection acts in the wild. For example, the latitudinal pattern in D. melanogaster is usually assumed to be due to temperature, but the cellular pattern does not match that seen in laboratory selection at different temperatures. [source] | |||||||||||||