Electrical conductivity measured in atomic carbon chains

The first electrical conductivity measurements of monoatomic carbon chains are reported in this study. The chains were obtained by unraveling carbon atoms from graphene ribbons while an electrical current flowed through the ribbon and, successively, through the chain. The formation of the chains was accompanied by a characteristic drop in the electrical conductivity. The conductivity of carbon chains was much lower than previously predicted for ideal chains. First-principles calculations using both density functional and many-body perturbation theory show that strain in the chains determines the conductivity in a decisive way. Indeed, carbon chains are always under varying non-zero strain that transforms its atomic structure from cumulene to polyyne configuration, thus inducing a tunable band gap. The modified electronic structure and the characteristics of the contact to the graphitic periphery explain the low conductivity of the locally constrained carbon chain.Comment: 21 pages, 9 figure

The effect of short – term exercise on nitric oxide (NO) serum concentrations in overweight and obese women

Objective: The aims of the present study was to examine the effect of overweight and obesity on serum concentrations of nitric oxide metabolites and evaluate the differences of exercise induced NO production in obese and lean women. Materials and Methods: The study groups consisted of 154 women including 102 obese and 24 overweight patients and 28 lean controls. Serum concentrations of nitric oxide metabolites were measured before and after exercise with the use of ELISA kits. The serum concentrations of lactate before and after exercise were measured with the use of strip test (ACCUSPORT analyzer). Serum concentration of insulin was measured with the use of RIA. Plasma glucose, cholesterol, HDL cholesterol and triglicerydes were determined by enzymatic procedure. Impedance analysis (Bodystat) was used to determine body composition. Results: Serum concentration of NO in overweight group and obese group was significantly higher when compared to controls, p<0.05 and p<0.01, respectively. There was no difference in levels of NO between overweight and obese groups .During exercise NO concentrations increased significantly in all groups and the post- exercise levels did not differ statistically in overweight and obese groups from that in controls. The value of NO was the lowest in obese group but there were no significant differences between obese, overweight and control groups. Conclusions: Obesity may attenuate the exercise - induced endothelial NO release

The use of geoelectrical method in preliminary investigation of the Fredro Family's iron mine adit in the village of Cisna, the Bieszczady Mountains, SE Poland

The study over the historical Rose iron mine adit were performed to find and map its location. In order to locate the exploited adit the resistivity imaging method was applied. Measurements were carried out along six survey profiles perpendicularly intersecting the adit. Measurements done along first three profiles were performed with application of 5 m electrode spacing and the total length of electrode array reached 200 m. For the profiles 4th and 6th 10 m electrode spacing was applied what gave total profile length of 400 m. The 5th profile possessed 5m electrode spacing and total length of 470 m. Roll-along technique was designed on this profile. For all measurements the Sweden equipment Lund produced by ABEM company was applied. Each resistivity cross-section was obtained after the robust inversion using Res2Dinv software. The results showed high resistivity anomalies located in areas suspicious as the adit, beneath the main ridge of Mochnaczka-Jeleni Skok Mountain. Near the adit entrance known from the historical information, the main anomaly was disturbed, probably because of the collapse of a tunnel entrance which could be seen in terrain morphology. It is supposed that on further distances the adit retained its character, however, it can be filled with secondary deposits or flooded

The effect of weight loss on serum concentrations of nitric oxide induced by short - term exercise in obese women

Objective: The aim of present study was to examine the effect of weight loss comprising regular moderate physical activity on resting serum concentrations of nitric oxide metabolites and exercise induced NO release. Materials and Methods: The study was carried out in 43 obese women without additional diseases (age 41.8±11.9y, body weight 94.5±15.1kg, BMI 36.5±4.6kg/m2). All obese patients participated in a 3-month weight reduction programme that consisted of 1) a group instruction in behavioural and dietary methods of weight control every two weeks; 2) 1000-1400kcal/day balanced diet, and 3) moderate physical exercises (30 minutes, 3 times a week). Before and after treatment body mass and height were measured, body mass index (BMI) was calculated. Body composition was determined by impedance analysis using a Bodystat analyser. The serum concentration of nitric oxide metabolites before and after exercise was measured using spectrophotometry method by Griess. The serum concentrations of lactate before and after exercise were measured with the use of strip test (ACCUSPORT analyzer). Serum concentration of insulin was measured with the use of RIA. Plasma glucose, cholesterol, HDL cholesterol and triglicerydes were determined by enzymatic procedure. Results: The mean weight loss during treatment was 8.3±4.3 kg. We did not observe differences between resting serum concentrations of NO and lactate before and after weight loss. During exercise serum NO concentrations increased significantly both before and after weight loss treatment. After the weight reduction treatment, the time of exercise test increased significantly P<0.005, but there were no significant differences between the value of NO before and after weight loss. Conclusion: 3 – month regular physical activity and weight loss did not influence exercise-induced nitric oxide production

Application of a filtration- and isolation-by-size technique for the detection of circulating tumor cells in cutaneous melanoma

Analysis of circulating tumor cells (CTC) in the peripheral blood of cutaneous melanoma patients provides information on the metastatic process and potentially improves patient management. The isolation by size of epithelial tumor cells (ISET) is a direct method for CTC identification in which tumor cells are collected by filtration as a result of their large size. So far, ISET has been applied only to CTC detection from epithelial cancer patients, and the technique has never been applied to cutaneous melanoma patients. We herein investigated the presence of CTC by ISET in the peripheral blood of 140 subjects (87 with cutaneous melanomas, 10 subjects undergoing surgery for melanocytic nevi, 5 patients with non-melanoma skin tumors, and 38 healthy volunteers). The identification of the cells trapped in filters as CTC was supported by positivity for immunohistochemical markers and for tyrosinase mRNA by real-time RT-PCR. CTC were neither detected in the controls nor in the in situ melanoma group. In contrast, CTC were shown in 29% of patients with primary invasive melanoma and in 62.5% of metastatic melanoma patients (P&lt;0.01). CTC detection correlated with the presence of mRNA tyrosinase in blood samples, assayed by real-time RT-PCR (P=0.001). CTC detection corroborated by suitable molecular characterization may assist in the identification and monitoring of more appropriate therapies in melanoma patients. © 2010 The Society for Investigative Dermatology

Kidins220/ARMS binds to the B cell antigen receptor and regulates B cell development and activation

B cell antigen receptor (BCR) signaling is critical for B cell development and activation. Using mass spectrometry, we identified a protein kinase D\u2013interacting substrate of 220 kD (Kidins220)/ankyrin repeat\u2013rich membrane-spanning protein (ARMS) as a novel interaction partner of resting and stimulated BCR. Upon BCR stimulation, the interaction increases in a Src kinase\u2013independent manner. By knocking down Kidins220 in a B cell line and generating a conditional B cell\u2013specific Kidins220 knockout (B-KO) mouse strain, we show that Kidins220 couples the BCR to PLC\u3b32, Ca2+, and extracellular signal-regulated kinase (Erk) signaling. Consequently, BCR-mediated B cell activation was reduced in vitro and in vivo upon Kidins220 deletion. Furthermore, B cell development was impaired at stages where pre-BCR or BCR signaling is required. Most strikingly, \u3bb light chain\u2013positive B cells were reduced sixfold in the B-KO mice, genetically placing Kidins220 in the PLC\u3b32 pathway. Thus, our data indicate that Kidins220 positively regulates pre-BCR and BCR functionin

Epstein-Barr Virus-Encoded BARF1 Protein is a Decoy Receptor for Macrophage Colony Stimulating Factor and Interferes with Macrophage Differentiation and Activation

Epstein-Barr virus (EBV), like many other persistent herpes viruses, has acquired numerous mechanisms for subverting or evading immune surveillance. This study investigates the role of secreted EBV-encoded BARF1 protein (sBARF1) in creating an immune evasive microenvironment. Wild-type consensus BARF1 was expressed in the human 293 cell line and purified. This native hexameric sBARF1 had inhibitory capacity on macrophage colony stimulating factor (M-CSF)-stimulated, and not on granulocyte macrophage-colony stimulating factor (GM-CSF)-stimulated growth and differentiation of myeloid cells. Antibodies specific to hexameric sBARF1 were able to block this effect. M-CSF was shown to interact with sBARF1 via the protruding N-terminal loops involving Val38 and Ala84. Each BARF1 hexamer was capable of binding three M-CSF dimers. Mutations in the BARF1 loops greatly affected M-CSF interaction, and showed loss of growth inhibition. Analysis of the activation state of the M-CSF receptor c-fms and its downstream kinase pathways showed that sBARF1 prevented M-CSF-induced downstream phosphorylation. Since M-CSF is an important factor in macrophage differentiation, the effect of sBARF1 on the function of monocyte-derived macrophages was evaluated. sBARF1 affected overall survival and morphology and significantly reduced expression of macrophage differentiation surface markers such as CD14, CD11b, CD16, and CD169. Macrophages differentiating in the presence of sBARF1 showed impaired responses to lipopolysaccharide and decreased oxygen radical formation as well as reduced phagocytosis of apoptotic cells. In conclusion, EBV sBARF1 protein is a potent decoy receptor for M-CSF, hampering the function and differentiation of macrophages. These results suggest that sBARF1 contributes to the modulation of immune responses in the microenvironment of EBV-positive carcinoma