736 research outputs found
Electronic structure reconstruction by orbital symmetry breaking in IrTe2
We report an angle-resolved photoemission spectroscopy (ARPES) study on IrTe2
which exhibits an interesting lattice distortion below 270 K and becomes
triangular lattice superconductors by suppressing the distortion via chemical
substitution or intercalation. ARPES results at 300 K show multi-band Fermi
surfaces with six-fold symmetry which are basically consistent with band
structure calculations. At 20 K in the distorted phase, whereas the flower
shape of the outermost Fermi surface does not change from that at 300 K,
topology of the inner Fermi surfaces is strongly modified by the lattice
distortion. The Fermi surface reconstruction by the distortion depends on the
orbital character of the Fermi surfaces, suggesting importance of Ir 5d and/or
Te 5p orbital symmetry breaking.Comment: 4pages, 4figure
Three-Dimensional Fermi Surface of Overdoped La-Based Cuprates
We present a soft x-ray angle-resolved photoemission spectroscopy study of
the overdoped high-temperature superconductors LaSrCuO and
LaEuSrCuO. In-plane and out-of-plane components of
the Fermi surface are mapped by varying the photoemission angle and the
incident photon energy. No dispersion is observed along the nodal
direction, whereas a significant antinodal dispersion is identified.
Based on a tight-binding parametrization, we discuss the implications for the
density of states near the van-Hove singularity. Our results suggest that the
large electronic specific heat found in overdoped LaSrCuO can
not be assigned to the van-Hove singularity alone. We therefore propose quantum
criticality induced by a collapsing pseudogap phase as a plausible explanation
for observed enhancement of electronic specific heat
Important Roles of Te 5p and Ir 5d Spin-orbit Interactions on the Multi-band Electronic Structure of Triangular Lattice Superconductor Ir1-xPtxTe2
We report an angle-resolved photoemission spectroscopy (ARPES) study on a
triangular lattice superconductor IrPtTe in which the Ir-Ir
or Te-Te bond formation, the band Jahn-Teller effect, and the spin-orbit
interaction are cooperating and competing with one another. The Fermi surfaces
of the substituted system are qualitatively similar to the band structure
calculations for the undistorted IrTe with an upward chemical potential
shift due to electron doping. A combination of the ARPES and the band structure
calculations indicates that the Te spin-orbit interaction removes the
orbital degeneracy and induces type spin-orbit
coupling near the A point. The inner and outer Fermi surfaces are entangled by
the Te and Ir spin-orbit interactions which may provide exotic
superconductivity with singlet-triplet mixing.Comment: 10 pages, 4 figure
Spectromicroscopy of electronic phase separation in KFeSe superconductor
Structural phase separation in AFeSe system has been studied
by different experimental techniques, however, it should be important to know
how the electronic uniformity is influenced, on which length scale the
electronic phases coexist, and what is their spatial distribution. Here, we
have used novel scanning photoelectron microscopy (SPEM) to study the
electronic phase separation in KFeSe, providing a direct
measurement of the topological spatial distribution of the different electronic
phases. The SPEM results reveal a peculiar interconnected conducting
filamentary phase that is embedded in the insulating texture. The filamentary
structure with a particular topological geometry could be important for the
high T superconductivity in the presence of a phase with a large magnetic
moment in AFeSe materials.Comment: 14 pages,3 figure
Electrochemical titrations and reaction time courses monitored in situ by magnetic circular dichroism spectroscopy
Magnetic circular dichroism (MCD) spectra, at ultraviolet–visible or near-infrared wavelengths (185–2000 nm), contain the same transitions observed in conventional absorbance spectroscopy, but their bisignate nature and more stringent selection rules provide greatly enhanced resolution. Thus, they have proved to be invaluable in the study of many transition metal-containing proteins. For mainly technical reasons, MCD has been limited almost exclusively to the measurement of static samples. But the ability to employ the resolving power of MCD to follow changes at transition metal sites would be a potentially significant advance. We describe here the development of a cuvette holder that allows reagent injection and sample mixing within the 50-mm-diameter ambient temperature bore of an energized superconducting solenoid. This has allowed us, for the first time, to monitor time-resolved MCD resulting from in situ chemical manipulation of a metalloprotein sample. Furthermore, we report the parallel development of an electrochemical cell using a three-electrode configuration with physically separated working and counter electrodes, allowing true potentiometric titration to be performed within the bore of the MCD solenoid
Cytokine responses of intraepithelial lymphocytes are regulated by histamine H2 receptor
Backgrounds. Histamine participates in the immune regulation of several gastrointestinal diseases. However, the effect of histamine on intestinal intraepithelial lymphocytes (IELs), the front line of intestinal mucosal immune system, is not well-understood. We examined whether histamine has a direct effect on cytokine production by IELs and the involvement of histamine receptor subtypes. Methods. Murine IELs were activated by PMA plus ionomycin with/without histamine. Secreted cytokines were measured and compared with those of splenocytes. Intracellular cytokines were detected by flow cytometory. Expression of histamine receptor subtypes in IELs was examined by RT-PCR. Results. Histamine H1 receptor (H1R), H2R, and H4R, but not H3R mRNA were expressed on IELs. Histamine significantly decreased Th1-cytokine (IFN-γ, TNF-α, and IL-2) and also IL-4 production in IELs as well as splenocytes. The selective H2R antagonist famotidine, but not the H1R antagonist pyrilamine nor the H3R/H4R antagonist thioperamide, competes with the inhibitory effect of histamine on these cytokine production in IELs. These suppressive effects of histamine were mimicked by a selective H2R/H4R agonist dimaprit. Further, these suppressive effects of histamine for Th1-cytokine and IL-4 did not accompany with the enhancement of IL-10 production nor IL-10 mRNA level in IELs. Intracellular cytokine analysis revealed that the number of IFN-γ-producingαβ T cells was significantly reduced by histamine in IELs. Conclusions. Histamine has a direct suppressive effect on IEL-derived cytokines via H2R, which would have a crucial role in the suppression of local immunoregulation in the intestinal epithelium.浜松医科大学学位論文 医博第549号(平成21年3月18日
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Genetic analysis reveals a hierarchy of interactions between polycystin-encoding genes and genes controlling cilia function during left-right determination
During mammalian development, left-right (L-R) asymmetry is established by a cilia-driven leftward fluid flow within a midline embryonic cavity called the node. This ‘nodal flow’ is detected by peripherally-located crown cells that each assemble a primary cilium which contain the putative Ca2+ channel PKD2. The interaction of flow and crown cell cilia promotes left side-specific expression of Nodal in the lateral plate mesoderm (LPM). Whilst the PKD2-interacting protein PKD1L1 has also been implicated in L-R patterning, the underlying mechanism by which flow is detected and the genetic relationship between Polycystin function and asymmetric gene expression remains unknown. Here, we characterize a Pkd1l1 mutant line in which Nodal is activated bilaterally, suggesting that PKD1L1 is not required for LPM Nodal pathway activation per se, but rather to restrict Nodal to the left side downstream of nodal flow. Epistasis analysis shows that Pkd1l1 acts as an upstream genetic repressor of Pkd2. This study therefore provides a genetic pathway for the early stages of L-R determination. Moreover, using a system in which cultured cells are supplied artificial flow, we demonstrate that PKD1L1 is sufficient to mediate a Ca2+ signaling response after flow stimulation. Finally, we show that an extracellular PKD domain within PKD1L1 is crucial for PKD1L1 function; as such, destabilizing the domain causes L-R defects in the mouse. Our demonstration that PKD1L1 protein can mediate a response to flow coheres with a mechanosensation model of flow sensation in which the force of fluid flow drives asymmetric gene expression in the embryo
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