6,244 research outputs found
TAZ Suppresses NFAT5 Activity through Tyrosine Phosphorylation
Transcriptional coactivator with PDZ-binding motif (TAZ) physically interacts with a variety of transcription factors and modulates their activities involved in cell proliferation and mesenchymal stem cell differentiation. TAZ is highly expressed in the kidney, and a deficiency of this protein results in multiple renal cysts and urinary concentration defects; however, the molecular functions of TAZ in renal cells remain largely unknown. In this study, we examined the effects of osmotic stress on TAZ expression and activity in renal cells. We found that hyperosmotic stress selectively increased protein phosphorylation at tyrosine 316 of TAZ and that this was enhanced by c-Abl activation in response to hyperosmotic stress. Interestingly, phosphorylated TAZ physically interacted with nuclear factor of activated T cells 5 (NFAT5), a major osmoregulatory transcription factor, and subsequently suppressed DNA binding and transcriptional activity of NFAT5. Furthermore, TAZ deficiency elicited an increase in NFAT5 activity in vitro and in vivo, which then reverted to basal levels following restoration of wild-type TAZ but not mutant TAZ (Y316F). Collectively, the data suggest that TAZ modulates cellular responses to hyperosmotic stress through fine-tuning of NFAT5 activity via tyrosine phosphorylation.open3
Half-metallic antiferromagnets in double perovskites: LaAVRuO (A=Ca, Sr, and Ba)
Based on the theoretical exploration of electronic structures, we propose
that the ordered double perovskites LaAVRuO and LaVO/ARuO (001)
superlattice (A = Ca, Sr and Ba) are strong candidates for half-metallic (HM)
antiferromagnets (AFMs). %LaAVRuO and LaVO/ARuO have the %100% spin
polarizations at the Fermi level but with zero %total magnetic moments. We have
shown that the HM-AFM nature in LaAVRuO is very robust regardless of (i)
divalent ion replacement at A-sites, (ii) oxygen site relaxation, (iii) the
inclusion of the Coulomb correlation, and (iv) cation disorder. A type of the
double exchange interaction is expected to be responsible for the
half-metallicity and the antiferromagnetism in these systems.Comment: 4 pages, 4 figure
Calorimetric Evidence for Nodes in the Overdoped Ba(FeCo)As
We present low-temperature specific heat of the electron-doped
Ba(FeCo)As, which does not show any indication of
an upturn down to 400 mK, the lowest measuring temperature. The lack of a
Schottky-like feature at low temperatures or in magnetic fields up to 9 Tesla
enables us to identify enhanced low-temperature quasiparticle excitations and
to study anisotropy in the linear term of the specific heat. Our results can
not be explained by a single or multiple isotropic superconducting gap, but are
consistent with multi-gap superconductivity with nodes on at least one Fermi
surface sheet.Comment: 5 pages 4 figure
Crystalline electric field effects in Ce 3 core-level spectra of heavy-fermion systems: Hard X-ray photoemission spectroscopy on CeNiCoGe
High-resolution hard X-ray photoemission measurements have been performed to
clarify the electronic structure originating from the strong correlation
between electrons in bulk Ce 3 core-level spectra of
CeNiCoGe (0 1). In the Ce 3
core-level spectra, the variation of satellite structures ( peaks) shows
that the hybridization strength between Ce 4- and conduction electrons
gradually increases with Co concentration in good agreement with the results of
Ce 3 and 4 resonant photoemission spectroscopies. Particularly, in
Ce 3 core-level spectra, the multiplet structures of peaks
systematically change with the degeneracy of -states which originates from
crystalline electric field effects.Comment: 10 pages, 4 figures, to appear in Physical Review
The effect of umbilical cord blood derived mesenchymal stem cells in monocrotaline-induced pulmonary artery hypertension rats
Pulmonary arterial hypertension (PAH) causes right ventricular failure due to a gradual increase in pulmonary vascular resistance. The purposes of this study were to confirm the engraftment of human umbilical cord blood-mesenchymal stem cells (hUCB-MSCs) placed in the correct place in the lung and research on changes of hemodynamics, pulmonary pathology, immunomodulation and several gene expressions in monocrotaline (MCT)induced PAH rat models after hUCB-MSCs transfusion. The rats were grouped as follows: the control (C) group; the M group (MCT 60 mg/kg); the U group (hUCB-MSCs transfusion). They received transfusions via the external jugular vein a week after MCT injection. The mean right ventricular pressure (RVP) was significantly reduced in the U group after the 2 week. The indicators of RV hypertrophy were significantly reduced in the U group at week 4. Reduced medial wall thickness in the pulmonary arteriole was noted in the U group at week 4. Reduced number of intra-acinar muscular pulmonary arteries was observed in the U group after 2 week. Protein expressions such as endothelin (ET)-1, endothelin receptor A (ERA), endothelial nitric oxide synthase (eNOS) and matrix metalloproteinase (MMP)-2 significantly decreased at week 4. The decreased levels of ERA, eNOS and MMP-2 immunoreactivity were noted by immnohistochemical staining. After hUCB-MSCs were administered, there were the improvement of RVH and mean RVP. Reductions in several protein expressions and immunomodulation were also detected. It is suggested that hUCB-MSCs may be a promising therapeutic option for PAH.1174Ysciescopu
Expression of osteopontin in calcified coronary atherosclerotic plaques.
Advanced atherosclerosis is often associated with dystrophic calcification and remodeling of extracellular matrix of vascular wall. Recently many studies have documented a general relationship between calcification and severity of coronary disease, and discussed the feasibility of electron beam computed tomography for detecting and quantifying the coronary artery calcification in the patients. The present study investigated the expression and the localization of osteopontin, one of noncollagenous bone matrix protein, within the calcified coronary arteries. Autopsy-derived coronary artery specimens were scanned and reconstructed to visualize the pattern of coronary calcification using a novel microscopic computed tomography technique. The localization of the osteopontin were evaluated by immunohistochemial stain with LF7. The present study showed that the pattern of coronary calcification is variable and the expression of osteopontin is localized mainly to calcified lesion. The smooth muscle cells in addition to macrophage expressed osteopontin protein in human coronary atherosclerotic plaques. Soluble osteopontin released near to the sites of vascular calcification may represent an adaptive mechanism aimed at regulating the process of vascular calcification
β-catenin activation down-regulates cell-cell junction-related genes and induces epithelial-to-mesenchymal transition in colorectal cancers
WNT signaling activation in colorectal cancers (CRCs) occurs through APC inactivation or β-catenin mutations. Both processes promote β-catenin nuclear accumulation, which up-regulates epithelial-to-mesenchymal transition (EMT). We investigated β-catenin localization, transcriptome, and phenotypic differences of HCT116 cells containing a wild-type (HCT116-WT) or mutant β-catenin allele (HCT116-MT), or parental cells with both WT and mutant alleles (HCT116-P). We then analyzed β-catenin expression and associated phenotypes in CRC tissues. Wild-type β-catenin showed membranous localization, whereas mutant showed nuclear localization; both nuclear and non-nuclear localization were observed in HCT116-P. Microarray analysis revealed down-regulation of Claudin-7 and E-cadherin in HCT116-MT vs. HCT116-WT. Claudin-7 was also down-regulated in HCT116-P vs. HCT116-WT without E-cadherin dysregulation. We found that ZEB1 is a critical EMT factor for mutant β-catenin-mediated loss of E-cadherin and Claudin-7 in HCT116-P and HCT116-MT cells. We also demonstrated that E-cadherin binds to both WT and mutant β-catenin, and loss of E-cadherin releases β-catenin from the cell membrane and leads to its degradation. Alteration of Claudin-7, as well as both Claudin-7 and E-cadherin respectively caused tight junction (TJ) impairment in HCT116-P, and dual loss of TJs and adherens junctions (AJs) in HCT116-MT. TJ loss increased cell motility, and subsequent AJ loss further up-regulated that. Immunohistochemistry analysis of 101 CRCs revealed high (14.9%), low (52.5%), and undetectable (32.6%) β-catenin nuclear expression, and high β-catenin nuclear expression was significantly correlated with overall survival of CRC patients (P = 0.009). Our findings suggest that β-catenin activation induces EMT progression by modifying cell-cell junctions, and thereby contributes to CRC aggressiveness
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