Origin of the increased velocities of domain wall motions in soft magnetic thin-film nanostripes beyond the velocity-breakdown regime

It is known that oscillatory domain-wall (DW) motions in soft magnetic thin-film nanostripes above the Walker critical field lead to a remarkable reduction in the average DW velocities. In a much-higher-field region beyond the velocity-breakdown regime, however, the DW velocities have been found to increase in response to a further increase of the applied field. We report on the physical origin and detailed mechanism of this unexpected behavior. We associate the mechanism with the serial dynamic processes of the nucleation of vortex-antivortex (V-AV) pairs inside the stripe or at its edges, the non-linear gyrotropic motions of Vs and AVs, and their annihilation process. The present results imply that a two-dimensional soliton model is required for adequate interpretation of DW motions in the linear- and oscillatory-DW-motion regimes as well as in the beyond-velocity-breakdown regime.Comment: 16 pages, 3 figure

Massive transfusion protocol: the reason it is necessary

Objective. The purpose of this study is to identify problems of emergency transfusion at the bedside and to determine need for massive transfusion protocol. Methods. We included patients who met the criteria for “trauma team activation” and were admitted to division of trauma. The amount of blood product transfused in each unit was investigated for balanced transfusion. We also investigated the compliance with assessment of blood consumption score. The correlation between the time elapsed from patient visit to first transfusion order and time elapsed from first transfusion order to transfusion start was analyzed. Finally, we investigated various factors which serve to influence the decision-making process regarding early transfusion order. Results. Ratio of packed Red blood cells (pRBC): Fresh frozen plasma (FFP) was well-balanced, but platelet transfusion done was much lower than pRBC and FFP in emergency room. The application of emergency blood release did not match the criteria of assessment of blood consumption (ABC) score. The time from the first transfusion order to the transfusion start was found to be constant irrespective of time from patient visit to first transfusion order. And, the time from the first transfusion order to transfusion start did not differ significantly among patients with early transfusion order and delayed transfusion order. Only systolic blood pressure of < 90 mmHg was identified as a major predictor for early transfusion order. Conclusion. Balanced transfusion is not easy and emergency transfusion could be delayed at the bedside. Integrated and systematic structures for massive transfusion protocol would be invaluable and indispensable

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Criterion for transformation of transverse domain wall to vortex or antivortex wall in soft magnetic thin-film nanostripes

We report on the criterion for the dynamic transformation of the internal structure of moving domain walls (DWs) in soft magnetic thin-film nanostripes above the Walker threshold field, Hw. In order for the process of transformation from transverse wall (TW) to vortex wall (VW) or antivortex wall (AVW) occurs, the edge-soliton core of the TW-type DW should grow sufficiently to the full width at half maximum of the out-of-plane magnetizations of the core area of the stabilized vortex (or antivortex) by moving inward along the transverse (width) direction. Upon completion of the nucleation of the vortex (antivortex) core, the VW (AVW) is stabilized, and then its core accompanies the gyrotropic motion in a potential well (hill) of a given nanostripe. Field strengths exceeding the Hw, which is the onset field of DW velocity breakdown, are not sufficient but necessary conditions for dynamic DW transformation

LAPTM5 overexpression causes mitochondrial damage and apoptosis

Human lysosomal-associated protein multispanning membrane 5 (LAPTM5) was identified by an ordered differential display-polymerase chain reaction (ODD-PCR) as an up-regulated cDNA fragment during 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced differentiation of U937 cells into monocytes/macrophages. After TPA-treatment, the levels of LAPTM5 mRNA and protein increased and reached a maximum at 18-36 h. In healthy human tissues, LAPTM5 mRNA was expressed at high levels in hematopoietic cells and tissues, at low levels in the lung and fetal liver, and was not detected in other non-hematopoietic tissues. LAPTM5 mRNA was detected in immature malignant cells of myeloid lineage, such as K562, HL-60, U937, and THP-1 cells, and in unstimulated peripheral T cells, but was absent or barely detectable in lymphoid malignant or non-hematopoietic malignant cells. The LAPTM5 level in HL-60 cells increased more significantly during TPA-induced monocyte/macrophage differentiation than during DMSO-induced granulocyte differentiation. Ectopic expression of GFP-LAPTM5 or LAPTM5 in HeLa cells exhibited the localization of LAPTM5 to the lysosome. In HeLa cells overexpressing LAPTM5, the Mcl-1 and Bid levels declined markedly and apoptosis was induced via Bak activation, Δψm loss, activation of caspase-9, -8 and -3, and PARP degradation without accompanying necrosis. However, these LAPTM5-induced apoptotic events except for the decline of Bid level were completely abrogated by concomitant overexpression of Mcl-1. The pan-caspase inhibitor (z-VAD-fmk) could suppress the LAPTM5-induced apoptotic sub-G1 peak by ~40% but failed to block the induced Δψm loss, whereas the broad-range inhibitor of cathepsins (Cathepsin Inhibitor I) could suppress the LAPTM5-induced apoptotic sub-G1 peak and Δψm loss, by ~22% and ~23%, respectively, suggesting that the LAPTM5-mediated Δψm loss was exerted at least in part in a cathepsin-dependent manner. Together, these results demonstrate that ectopic overexpression of LAPTM5 in HeLa cells induced apoptosis via cleavage of Mcl-1 and Bid by a LAPTM5-associated lysosomal pathway, and subsequent activation of the mitochondria-dependent caspase cascade