The Significance of Epithelial-to-Mesenchymal Transition for Circulating Tumor Cells

Epithelial to mesenchymal transition (EMT) is a process involved in embryonic development, but it also plays a role in remote metastasis formation in tumor diseases. During this process cells lose their epithelial features and adopt characteristics of mesenchymal cells. Thereby single tumor cells, which dissolve from the primary tumor, are enabled to invade the blood vessels and travel throughout the body as so called “circulating tumor cells” (CTCs). After leaving the blood stream the reverse process of EMT, the mesenchymal to epithelial transition (MET) helps the cells to seed in different tissues, thereby generating the bud of metastasis formation. As metastasis is the main reason for tumor-associated death, CTCs and the EMT process are in the focus of research in recent years. This review summarizes what was already found out about the molecular mechanisms driving EMT, the consequences of EMT for tumor cell detection, and suitable markers for the detection of CTCs which underwent EMT. The research work done in this field could open new roads towards combating cancer.     

Design of an Ultrafast G Protein Switch Based on a Mouse Melanopsin Variant

The primary goal of optogenetics is the light-controlled noninvasive and specific manipulation of various cellular processes. Herein, we present a hybrid strategy for targeted protein engineering combining computational techniques with electrophysiological and UV/visible spectroscopic experiments. We validated our concept for channelrhodopsin-2 and applied it to modify the less-well-studied vertebrate opsin melanopsin. Melanopsin is a promising optogenetic tool that functions as a selective molecular light switch for G protein-coupled receptor pathways. Thus, we constructed a model of the melanopsin G_q protein complex and predicted an absorption maximum shift of the Y211F variant. This variant displays a narrow blue-shifted action spectrum and twofold faster deactivation kinetics compared to wild-type melanopsin on G protein-coupled inward rectifying K⁺ (GIRK) channels in HEK293 cells. Furthermore, we verified the in vivo activity and optogenetic potential for the variant in mice. Thus, we propose that our developed concept will be generally applicable to designing optogenetic tools.     

Prototype and Chimera-Type Galectins in Placentas with Spontaneous and Recurrent Miscarriages

Galectins are galactose binding proteins and, in addition, factors for a wide range of pathologies in pregnancy. We have analyzed the expression of prototype (gal-1, -2, -7, -10) and chimera-type (gal-3) galectins in the placenta in cases of spontaneous abortions (SPA) and recurrent abortions (RA) in the first trimester. Fifteen placental samples from healthy pregnancies were used as a control group. Nine placentas were examined for spontaneous abortions, and 12 placentas for recurrent abortions. For differentiation and evaluation of different cell types of galectin-expression in the decidua, immunofluorescence was used. For all investigated prototype galectins (gal-1, -2, -7, -10) in SPA and RA placenta trophoblast cells the expression is significantly decreased. In the decidua/extravillous trophoblast only gal-2 expression was significantly lowered, which could be connected to its role in angiogenesis. In trophoblasts in first-trimester placentas and in cases of SPA and RA, prototype galectins are altered in the same way. We suspect prototype galectins have a similar function in placental tissue because of their common biochemical structure. Expression of galectin 3 as a chimera type galectin was not found to be significantly altered in abortive placentas.     

Reconfigurable CMOS with undoped silicon nanowire midgap Schottky-barrier FETs

In this paper we report on a newly developed multi-gate nanowire-field-effect device (NWFET) in which the transistor type (i.e. PMOS and NMOS) is freely selectable by the application of a control-voltage. This significantly adds to flexibility in design of integrated circuits and their fabrication, respectively. We will show, that the use of midgap Schottky-barrier source and drain contacts are the key enabler for this device concept to be functional. A fully functional freely configurable CMOS-NWFET inverter circuit is presented, demonstrating the capability of this SOI technology platform. All this makes the presented NWFET-technology suitable for the fabrication multi-purpose devices for many applications.     

Non-monotonic lattice parameter variation with crystallite size in nanocrystalline solids

An anomalous dependence of the lattice parameter on the crystallite size of nanocrystalline ball-milled powders of metals was observed: lattice contraction followed by lattice expansion with decreasing crystallite size. These data were determined by application of detailed X-ray diffraction measurements. To this end the lattice parameters of the metals investigated – nickel, copper, iron and tungsten – were precisely determined by correcting for influences of stacking faults, in the face-centred cubic metals, as well as by correcting for instrument-related aberrations. The non-monotonic variation of the lattice constant was interpreted as the result of two competing mechanisms: interface-stress-induced contraction vs. expansion as a result of the stress field generated at the crystallite boundary due to the increased excess free volume in the crystallite boundary upon decreasing crystallite size.     

Microtensile testing of submicrometer thick functional polymer samples

Organic electronic devices are currently being introduced in commercial applications such as flexible displays. Due to the mechanical loading of these devices during bending, it is important to know the mechanical properties in order to assess reliability. It is therefore essential to develop experimental setups for the mechanical characterization of submicrometer thick functional polymer layers. In this paper a new microtensile approach is presented along with first results for Young's modulus of polyimide (PI) and the conductive polymer PEDOT:PSS obtained using this method. The microtensile specimen are made of a bilayer consisting of PI as the substrate layer and of a submicron layer of PEDOT:PSS deposited on top of it. The mechanical properties are derived from comparison of measurements performed on samples with and without the functional layer and by varying this layer's thickness. A thorough error analysis is also presented to provide an overview of the precision inherent in this approach. The experiments yield Young's moduli of 3.28 ± 0.34 GPa for PI and of 4.51 ± 0.34 GPa for PEDOT:PSS.