Ostwald ripening of rod-shaped α-Fe particles in a Cu matrix

The coarsening behavior of rod-shaped α-Fe particles in Cu–1.0 wt.% Fe and Cu–1.0 wt.% Fe–1.2 wt.% Sb alloys during aging at 700 °C has been studied by transmission electron microscopy and electric resistivity. The kinetics of the decay of supersaturation with aging time t for both alloys coincide with the t−1/3 law. The coarsening kinetics of the cylindrical radius of the Fe particles obey the t1/3 law. Using the Lifshitz–Slyozov–Wagner theory modified for the case of rod-shaped particles by Speich and Oriani, the maximum value of the Cu/α-Fe interfacial energy γ and the volume diffusivity D of Fe in Cu for the Cu−Fe alloy are independently derived to be 1.3 J/m2 and 3.9×10−16 m2/s. Adding Sb to the Cu−Fe alloy decreases the values of γ and D

Energy distribution of precipitating electrons estimated from optical and cosmic noise absorption measurements

International audienceThis study is a statistical analysis on energy distribution of precipitating electrons, based on CNA (cosmic noise absorption) data obtained from the 256-element imaging riometer in Poker Flat, Alaska (65.11° N, 147.42° W), and optical data measured with an MSP (Meridian Scanning Photometer) over 79 days during the winter periods from 1996 to 1998. On the assumption that energy distributions of precipitating electrons represent Maxwellian distributions, CNA is estimated based on the observation data of auroral 427.8-nm and 630.0-nm emissions, as well as the average atmospheric model, and compared with the actual observation data. Although the observation data have a broad distribution, they show systematically larger CNA than the model estimate. CNA determination using kappa or double Maxwellian distributions, instead of Maxwellian distributions, better explains the distribution of observed CNA data. Kappa distributions represent a typical energy distribution of electrons in the plasma sheet of the magnetosphere, the source region of precipitating electrons. Pure kappas are more likely during quiet times ? and quiet times are more likely than active times. This result suggests that the energy distribution of precipitating electrons reflects the energy distribution of electrons in the plasma sheet. Key words. Ionosphere (auroral ionosphere; particle precipitation; polar ionosphere

Human pluripotent embryonal carcinoma NTERA2 cl.D1 cells maintain their typical morphology in an angiomyogenic medium

BACKGROUND: Pluripotent embryonal carcinomas are good potential models, to study, "in vitro," the mechanisms that control differentiation during embryogenesis. The NTERA2cl.D1 (NT2/D1) cell line is a well known system of ectodermal differentiation. Retinoic acid (RA) induces a dorsal pattern of differentiation (essentially neurons) and bone morphogenetic protein (BMP) or hexamethylenebisacetamide (HMBA) induces a more ventral (epidermal) pattern of differentiation. However, whether these human cells could give rise to mesoderm derivatives as their counterpart in mouse remained elusive. We analyzed the morphological characteristics and transcriptional activation of genes pertinent in cardiac muscle and endothelium differentiation, during the growth of NT2/D1 cells in an inductive angiomyogenic medium with or without Bone Morphogenetic Protein 2 (BMP2). RESULTS: Our experiments showed that NT2/D1 maintains their typical actin organization in angiomyogenic medium. Although the beta myosin heavy chain gene was never detected, all the other 15 genes analyzed maintained their expression throughout the time course of the experiment. Among them were early and late cardiac, endothelial, neuronal and teratocarcinoma genes. CONCLUSION: Our results suggest that despite the NT2/D1 cells natural tendency to differentiate into neuroectodermal lineages, they can activate genes of mesodermal lineages. Therefore, we believe that these pluripotent cells might still be a good model to study biological development of mesodermal derivatives, provided the right culture conditions are met

A Comparative Analysis of Extra-Embryonic Endoderm Cell Lines

Prior to gastrulation in the mouse, all endodermal cells arise from the primitive endoderm of the blastocyst stage embryo. Primitive endoderm and its derivatives are generally referred to as extra-embryonic endoderm (ExEn) because the majority of these cells contribute to extra-embryonic lineages encompassing the visceral endoderm (VE) and the parietal endoderm (PE). During gastrulation, the definitive endoderm (DE) forms by ingression of cells from the epiblast. The DE comprises most of the cells of the gut and its accessory organs. Despite their different origins and fates, there is a surprising amount of overlap in marker expression between the ExEn and DE, making it difficult to distinguish between these cell types by marker analysis. This is significant for two main reasons. First, because endodermal organs, such as the liver and pancreas, play important physiological roles in adult animals, much experimental effort has been directed in recent years toward the establishment of protocols for the efficient derivation of endodermal cell types in vitro. Conversely, factors secreted by the VE play pivotal roles that cannot be attributed to the DE in early axis formation, heart formation and the patterning of the anterior nervous system. Thus, efforts in both of these areas have been hampered by a lack of markers that clearly distinguish between ExEn and DE. To further understand the ExEn we have undertaken a comparative analysis of three ExEn-like cell lines (END2, PYS2 and XEN). PYS2 cells are derived from embryonal carcinomas (EC) of 129 strain mice and have been characterized as parietal endoderm-like [1], END2 cells are derived from P19 ECs and described as visceral endoderm-like, while XEN cells are derived from blastocyst stage embryos and are described as primitive endoderm-like. Our analysis suggests that none of these cell lines represent a bona fide single in vivo lineage. Both PYS2 and XEN cells represent mixed populations expressing markers for several ExEn lineages. Conversely END2 cells, which were previously characterized as VE-like, fail to express many markers that are widely expressed in the VE, but instead express markers for only a subset of the VE, the anterior visceral endoderm. In addition END2 cells also express markers for the PE. We extended these observations with microarray analysis which was used to probe and refine previously published data sets of genes proposed to distinguish between DE and VE. Finally, genome-wide pathway analysis revealed that SMAD-independent TGFbeta signaling through a TAK1/p38/JNK or TAK1/NLK pathway may represent one mode of intracellular signaling shared by all three of these lines, and suggests that factors downstream of these pathways may mediate some functions of the ExEn. These studies represent the first step in the development of XEN cells as a powerful molecular genetic tool to study the endodermal signals that mediate the important developmental functions of the extra-embryonic endoderm. Our data refine our current knowledge of markers that distinguish various subtypes of endoderm. In addition, pathway analysis suggests that the ExEn may mediate some of its functions through a non-classical MAP Kinase signaling pathway downstream of TAK1