291 research outputs found
Edge Shear Flows and Particle Transport near the Density Limit in the HL-2A Tokamak
Edge shear flow and its effect on regulating turbulent transport have long
been suspected to play an important role in plasmas operating near the
Greenwald density limit . In this study, equilibrium profiles as well as
the turbulent particle flux and Reynolds stress across the separatrix in the
HL-2A tokamak are examined as is approached in ohmic L-mode discharges.
As the normalized line-averaged density is raised, the
shearing rate of the mean poloidal flow drops, and the
turbulent drive for the low-frequency zonal flow (the Reynolds power ) collapses. Correspondingly, the turbulent particle
transport increases drastically with increasing collision rates. The geodesic
acoustic modes (GAMs) gain more energy from the ambient turbulence at higher
densities, but have smaller shearing rate than low-frequency zonal flows. The
increased density also introduces decreased adiabaticity which not only
enhances the particle transport but is also related to a reduction in the
eddy-tilting and the Reynolds power. Both effects may lead to the cooling of
edge plasmas and therefore the onset of MHD instabilities that limit the plasma
density
Constraining parameter space in type-II two-Higgs doublet model in light of a 126 GeV Higgs boson
We explore the implications of a 126 GeV Higgs boson indicated by the recent
LHC results for two-Higgs doublet model (2HDM). Identifying the 126 GeV Higgs
boson as either the lighter or heavier of CP even neutral Higgs bosons in 2HDM,
we examine how the masses of Higgs fields and mixing parameters can be
constrained by the theoretical conditions and experimental constraints. The
theoretical conditions taken into account are the vacuum stability,
perturbativity and unitarity required to be satisfied up to a cut-off scale. We
also show how bounds on the masses of Higgs bosons and mixing parameters depend
on the cut-off scale. In addition, we investigate whether the allowed regions
of parameter space can accommodate particularly the enhanced di-photon signals,
ZZ* and WW* decay modes of the Higgs boson, and examine the prediction of the
signal strength of Z{\gamma} decay mode for the allowed regions of the
parameter space.Comment: To be published in JHEP, 20 pages, 11 figures, Figures and results
are updated for the recent LHC result
p150 ADAR1 isoform involved in maintenance of HeLa cell proliferation
BACKGROUND: RNA-specific adenosine deaminase ADAR1 is ubiquitously expressed in a variety of mammalian cells and tissues. Although its physiological importance in non-nervous tissues has been confirmed by analysis of null mutation phenotypes, few endogenous editing substrates have been identified in numerous peripheral tissues and biological function of ADAR1 has not been fully understood. METHODS: A conditional site-specific, ribozyme-based gene knock-down strategy was utilized to study the function of full-length isoform of ADAR1 (p150 protein) in HeLa cell. Double-stable HeLa cell lines were developed by transfecting HeLa Tet-On cells with a pTRE-derived plasmid that can express a hammerhead ribozyme against mRNA of p150 ADAR1 isoform under induction condition. Semi-quantitative RT-PCR and Western blotting were performed to measure the expression of p150 in selected cell clones. Cell proliferation was evaluated by means of MTT assay and growth curve analysis. Cellular morphological changes were observed under light microscope. Flow Cytometry was used for cell cycle analysis. Growth rate of cell transplants in BALB/c nude mice was also investigated. RESULTS: Both HeLa cell proliferation in vitro and the growth rate of transplanted HeLa cell-derived tumors in nude mice in vivo were significantly inhibited due to reduced expression of ADAR1 p150. Additionally, cell cycle analysis showed that cell progression from G1 phase to S phase was retarded in the ADAR1 p150 suppressed cells. CONCLUSION: Our results suggest that normal expression and functioning of p150 ADAR1 is essential for the maintenance of proper cell growth. The mechanisms underlying ADAR1's action might include both editing of currently unknown double-stranded RNAs and interacting with other cellular dsRNA-related processes
LHC diphoton Higgs signal and top quark forward-backward asymmetry in quasi-inert Higgs doublet model
In the quasi-inert Higgs doublet model, we study the LHC diphoton rate for a
standard model-like Higgs boson and the top quark forward-backward asymmetry at
Tevatron. Taking into account the constraints from the vacuum stability,
unitarity, electroweak precision tests, flavor physics and the related
experimental data of top quark, we find that compared with the standard model
prediction, the diphoton rate of Higgs boson at LHC can be enhanced due to the
light charged Higgs contributions, while the measurement of the top quark
forward-backward asymmetry at Tevatron can be explained to within due
to the non-standard model neutral Higgs bosons contributions. Finally, the
correlations between the two observables are discussed.Comment: 14 pages, 5 figues. Version to appear in JHEP, some references adde
Transcriptome and Proteome Exploration to Model Translation Efficiency and Protein Stability in Lactococcus lactis
This genome-scale study analysed the various parameters influencing protein levels in cells. To achieve this goal, the model bacterium Lactococcus lactis was grown at steady state in continuous cultures at different growth rates, and proteomic and transcriptomic data were thoroughly compared. Ratios of mRNA to protein were highly variable among proteins but also, for a given gene, between the different growth conditions. The modeling of cellular processes combined with a data fitting modeling approach allowed both translation efficiencies and degradation rates to be estimated for each protein in each growth condition. Estimated translational efficiencies and degradation rates strongly differed between proteins and were tested for their biological significance through statistical correlations with relevant parameters such as codon or amino acid bias. These efficiencies and degradation rates were not constant in all growth conditions and were inversely proportional to the growth rate, indicating a more efficient translation at low growth rate but an antagonistic higher rate of protein degradation. Estimated protein median half-lives ranged from 23 to 224 min, underlying the importance of protein degradation notably at low growth rates. The regulation of intracellular protein level was analysed through regulatory coefficient calculations, revealing a complex control depending on protein and growth conditions. The modeling approach enabled translational efficiencies and protein degradation rates to be estimated, two biological parameters extremely difficult to determine experimentally and generally lacking in bacteria. This method is generic and can now be extended to other environments and/or other micro-organisms
On-chip Single Nanoparticle Detection and Sizing by Mode Splitting in an Ultra-high-Q Microresonator
The ability to detect and size individual nanoparticles with high resolution
is crucial to understanding behaviours of single particles and effectively
using their strong size-dependent properties to develop innovative products. We
report real-time, in-situ detection and sizing of single nanoparticles, down to
30 nm in radius, using mode-splitting in a monolithic ultra-high-Q
whispering-gallery-mode (WGM) microtoroid resonator. Particle binding splits a
WGM into two spectrally shifted resonance modes, forming a self-referenced
detection scheme. This technique provides superior noise suppression and
enables extracting accurate size information in a single-shot measurement. Our
method requires neither labelling of the particles nor apriori information on
their presence in the medium, providing an effective platform to study
nanoparticles at single particle resolution.Comment: 23 pages, 8 figure
The mitochondrial DNA 4,977-bp deletion and its implication in copy number alteration in colorectal cancer
<p>Abstract</p> <p>Background</p> <p>Qualitative and quantitative changes in human mitochondrial DNA (mtDNA) have been implicated in various cancer types. A 4,977 bp deletion in the major arch of the mitochondrial genome is one of the most common mutations associated with a variety of human diseases and aging.</p> <p>Methods</p> <p>We conducted a comprehensive study on clinical features and mtDNA of 104 colorectal cancer patients in the Wenzhou area of China. In particular, using a quantitative real time PCR method, we analyzed the 4,977 bp deletion and mtDNA content in tumor tissues and paired non-tumor areas from these patients.</p> <p>Results</p> <p>We found that the 4,977 bp deletion was more likely to be present in patients of younger age (≤65 years, p = 0.027). In patients with the 4,977 bp deletion, the deletion level decreased as the cancer stage advanced (p = 0.031). Moreover, mtDNA copy number in tumor tissues of patients with this deletion increased, both compared with that in adjacent non-tumor tissues and with in tumors of patients without the deletion. Such mtDNA content increase correlated with the levels of the 4,977 bp deletion and with cancer stage (p < 0.001).</p> <p>Conclusions</p> <p>Our study indicates that the mtDNA 4,977 bp deletion may play a role in the early stage of colorectal cancer, and it is also implicated in alteration of mtDNA content in cancer cells.</p
Bioavailability of Orally Administered rhGM-CSF: A Single-Dose, Randomized, Open-Label, Two-Period Crossover Trial
BACKGROUND: Recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) is usually administered by injection, and its oral administration in a clinical setting has been not yet reported. Here we demonstrate the bioavailability of orally administered rhGM-CSF in healthy volunteers. The rhGM-CSF was expressed in Bombyx mori expression system (BmrhGM-CSF). METHODS AND FINDINGS: Using a single-dose, randomized, open-label, two-period crossover clinical trial design, 19 healthy volunteers were orally administered with BmrhGM-CSF (8 microg/kg) and subcutaneously injected with rhGM-CSF (3.75 microg/kg) respectively. Serum samples were drawn at 0.0h, 0.5h ,0.75h,1.0h,1.5h,2.0h ,3.0h,4.0h,5.0h,6.0h,8.0h,10.0h and 12.0h after administrations. The hGM-CSF serum concentrations were determined by ELISA. The AUC was calculated using the trapezoid method. The relative bioavailability of BmrhGM-CSF was determined according to the AUC ratio of both orally administered and subcutaneously injected rhGM-CSF. Three volunteers were randomly selected from 15 orally administrated subjects with ELISA detectable values. Their serum samples at the 0.0h, 1.0h, 2.0h, 3.0h and 4.0h after the administrations were analyzed by Q-Trap MS/MS TOF. The different peaks were revealed by the spectrogram profile comparison of the 1.0h, 2.0h, 3.0h and 4.0h samples with that of the 0.0h sample, and further analyzed using both Enhanced Product Ion (EPI) scanning and Peptide Mass Fingerprinting Analysis. The rhGM-CSF was detected in the serum samples from 15 of 19 volunteers administrated with BmrhGM-CSF. Its bioavailability was observed at an average of 1.0%, with the highest of 3.1%. The rhGM-CSF peptide sequences in the serum samples were detected by MS analysis, and their sizes ranging from 2,039 to 7,336 Da. CONCLUSIONS: The results demonstrated that the oral administered BmrhGM-CSF was absorbed into the blood. This study provides an approach for an oral administration of rhGM-CSF protein in clinical settings. TRIAL REGISTRATION: www.chictr.orgChiCTR-TRC-00000107
Expression of interferon-γ in human adrenal gland and kidney tumours
It is known that interferon-γ (IFN-γ) is produced by activated T and NK lymphoid cells, mononuclear cells, and macrophage and dendritic cells. Our previous studies have shown that IFN-γ-like immunoreactivity also appears in human adrenal cortical tumour and phaeochromocytoma. To investigate whether human tumour cells can produce IFN-γ, we examined 429 biopsy specimens of 30 kinds of tumour and tumour-surrounding tissues in adrenal glands and in kidneys by using immunohistochemistry and in situ hybridisation. IFN-γ immunoactivity was shown in 34.3% of the adrenal cortical adenomas, 50% of the adrenal cortical carcinomas, 26.7% of the phaeochromocytomas, 26.7% of the clear cell renal cell carcinomas (RCCs), 22% of the adrenal cortexes and 40% of medullas adjacent to tumours. The positive samples and expression areas were well overlapped between the IFN-γ mRNA and the immunohistochemistry staining. Western blot analysis has further confirmed the immunohistochemistry results by showing a distinct IFN-γ band corresponding to 17.4 kDa in tissue extracts from adrenal cortical adenoma, phaeochromocytoma and clear cell RCCs. These results indicate that IFN-γ is produced by some types of tumour cells, suggesting it may play a dual role in the development of these tumours
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