22 research outputs found

    Coupled spin-charge-phonon fluctuation in the all-in/all-out antiferromagnet Cd2Os2O7

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    We report on a spin-charge fluctuation in the all-in/all-out pyrochlore magnet Cd2Os2O7, where the spin fluctuation is driven by the conduction of thermally excited electrons/holes and associated fluctuation of Os valence. The fluctuation exhibits an activation energy significantly greater than the spin-charge excitation gap and a peculiar frequency range of 10(6)-10(10) s(-1). These features are attributed to the hopping motion of carriers as small polarons in the insulating phase, where the polaron state is presumably induced by the magnetoelastic coupling via the strong spin-orbit interaction. Such a coupled spin-charge-phonon fluctuation manifests as a part of the metal-insulator transition that is extended over a wide temperature range due to the modest electron correlation comparable with other interactions characteristic for 5d-subshell systems

    CrkL directs ASAP1 to peripheral focal adhesions

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    Searching for proteins in platelets that can interact with the N-terminal SH3 domain of CrkL (using a combination of a pull-down assay followed by mass spectrometry), we have found that human platelets express an ADP-ribosylation factor (Arf)-specific GTPase-activating protein (GAP), ASAP1, as a CrkL-binding protein. In spreading platelets, most endogenous ASAP1 is localized at peripheral focal adhesions. To determine the physiologic significance of the CrkL-ASAP1 association, we overexpressed CrkL, ASAP1, or both in combination in COS7 cells. Unlike endogenous ASAP1 in platelets, overexpressed ASAP1 showed diffuse cytoplasmic distribution. However, when co-expressed with wild-type CrkL, both endogenous and expressed ASAP1 accumulated at CrkL-induced focal adhesions. An SH2-mutated CrkL, which cannot localize at focal adhesions, failed to recruit ASAP1 into focal adhesions. Thus, CrkL appears to be a lynchpin between ASAP1 and peripheral focal adhesions

    The Effect of Li x Ni2-x O2/Ni with Modification Method on Activity and Durability of Alkaline Water Electrolysis Anode

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    International audienceWater electrolysis requires durability during a fluctuating power supply in power-to-gas application with renewable energies. The previously developed lithiated NiO modified Ni (Li (x) Ni2-x O-2/Ni) has a high catalytic activity and durability during potential cycling, whereas the relatively high surface oxide resistance due to preparation of the oxidation at high temperature with a LiOH coating. In order to improve the catalytic activity, we proposed optimization of the oxide layer by thermal decomposition with various precursor coatings. The oxide layers prepared with acetate and nitrate precursors were dense and porous, respectively. The initial activity obtained from the acetate precursor electrode was higher than that of the nitrate precursor and the oxidation with the LiOH coating. Although the nitrate precursor electrode suffered from the same degradation as the Ni anode during potential cycling, the activity of the acetate precursor electrode as well as the oxidized electrode with the LiOH coating increased, and the activity for the former was almost the same as the initial Ni anode after 20,000 cycles. The lower preparation temperature of the acetate precursor would suppress the formation of the electron resistive nickel oxide between the base nickel and lithiated NiO, which was observed for the oxidized electrode with the LiOH coating as well. While the double-layer capacitance and redox peak around 1.3 V vs. RHE of the Ni and the nitrate precursor electrode significantly increased with Ni(IV) formation during potential cycling, those of the acetate precursor electrode slightly increased without any Ni(IV) formation. Therefore, the dense Li (x) Ni2-x O-2 prepared with acetate has a good electric conductivity and catalytic activity with a high durability during potential cycling as the anode of an alkaline water electrolyzer for renewable power sources

    School reform for positive behaviour support through collaborative learning: utilising lesson study for a learning community

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    Recent research has emphasised educating children about positive behaviours to overcome delinquency issues, but there is little clarification of what factors lead to positive behaviours. This study analyses factors that led to children’s positive behaviours at a junior high school in Japan, which experienced a dramatic turnaround after implementing school reform using Lesson Study for Learning Community (LSLC). In this study, the results of a mixed-methods analysis show that if children receive psychological support they are likely to psychologically support others and, similarly, those who receive concrete help tend to offer concrete help to others. To foster learning cultures in which this happens, it is critical to engage the entire school in appropriate changes: for example, teachers’ positive attitudes towards children and learning are important factors encouraging children to support others

    Novel and robust transplantation reveals the acquisition of polarized processes by cortical cells derived from mouse and human pluripotent stem cells

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    Current stem cell technologies have enabled the induction of cortical progenitors and neurons from embryonic stem cells (ESCs) and induced pluripotent stem cells in vitro. To understand the mechanisms underlying the acquisition of apico-basal polarity and the formation of processes associated with the stemness of cortical cells generated in monolayer culture, here, we developed a novel in utero transplantation system based on the moderate dissociation of adherens junctions in neuroepithelial tissue. This method enables (1) the incorporation of remarkably higher numbers of grafted cells and (2) quantitative morphological analyses at single-cell resolution, including time-lapse recording analyses. We then grafted cortical progenitors induced from mouse ESCs into the developing brain. Importantly, we revealed that the mode of process extension depends on the extrinsic apico-basal polarity of the host epithelial tissue, as well as on the intrinsic differentiation state of the grafted cells. Further, we successfully transplanted cortical progenitors induced from human ESCs, showing that our strategy enables investigation of the neurogenesis of human neural progenitors within the developing mouse cortex. Specifically, human cortical cells exhibit multiple features of radial migration. The robust transplantation method established here could be utilized both to uncover the missing gap between neurogenesis from ESCs and the tissue environment and as an in vivo model of normal and pathological human corticogenesis.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

    Novel and robust transplantation reveals the acquisition of polarized processes by cortical cells derived from mouse and human pluripotent stem cells

    No full text
    Current stem cell technologies have enabled the induction of cortical progenitors and neurons from embryonic stem cells (ESCs) and induced pluripotent stem cells in vitro. To understand the mechanisms underlying the acquisition of apico-basal polarity and the formation of processes associated with the stemness of cortical cells generated in monolayer culture, here, we developed a novel in utero transplantation system based on the moderate dissociation of adherens junctions in neuroepithelial tissue. This method enables (1) the incorporation of remarkably higher numbers of grafted cells and (2) quantitative morphological analyses at single-cell resolution, including time-lapse recording analyses. We then grafted cortical progenitors induced from mouse ESCs into the developing brain. Importantly, we revealed that the mode of process extension depends on the extrinsic apico-basal polarity of the host epithelial tissue, as well as on the intrinsic differentiation state of the grafted cells. Further, we successfully transplanted cortical progenitors induced from human ESCs, showing that our strategy enables investigation of the neurogenesis of human neural progenitors within the developing mouse cortex. Specifically, human cortical cells exhibit multiple features of radial migration. The robust transplantation method established here could be utilized both to uncover the missing gap between neurogenesis from ESCs and the tissue environment and as an in vivo model of normal and pathological human corticogenesis.status: publishe
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