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To investigate better GVHD prophylaxis in reduced intensity conditioning umbilical cord blood transplantation (RIC-UCBT), we compared transplant outcomes after UCBT among GvHD prophylaxes using the registry data. We selected patients transplanted for AML or ALL with a calcineurin inhibitor and methotrexate (MTX)/mycophenolate mofetil (MMF) combination. A total of 748 first RIC-UCBT between 2000 and 2012 (MTX+ group, 446, MMF+ group, 302) were included. The cumulative incidence of neutrophil and platelet counts higher than 50 000/μL was significantly better in the MMF+ group (relative risk (RR), 1.55; P<0.001: RR, 1.34; P=0.003, respectively). In multivariate analyses, the risk of grade II–IV and III–IV acute GvHD was significantly higher in the MMF+ group than in the MTX+ group (RR, 1.75; P<0.001: RR, 1.97; P=0.004, respectively). In disease-specific analyses of AML, the risk of relapse of high-risk disease was significantly lower in the MMF+ group (RR, 0.69; P=0.009), whereas no significant difference was observed in the risk of relapse-free and overall survival in high-risk disease. In patients with standard-risk disease, no significant differences were noted in the risk of relapse or survival between the MTX+ and MMF+ groups. Collectively, these results suggest that MMF-containing prophylaxis may be preferable in RIC-UCBT, particularly for high-risk disease.

To assess the impact of minimal residual disease (MRD) and tyrosine kinase inhibitor (TKI) administration on allogeneic hematopoietic cell transplantation (allo-HCT) for Ph-positive ALL (Ph+ALL), we retrospectively analyzed data from a registry database for 432 adult Ph+ALL patients in first CR (CR1) who received pre-transplant TKI administration. Negative MRD (MRD(−)) at allo-HCT was achieved in 277 patients. OS in patients transplanted in MRD(−) was significantly better than that in patients transplanted in MRD(+) (MRD(−): 67% vs MRD(+): 55% at 4 years; P=0.001). MRD(−) at allo-HCT was a significant risk factor for survival along with age at allo-HCT in multivariate analyses. Incidence of relapse in patients transplanted in MRD(−) was significantly lower than that in patients transplanted in MRD(+) (MRD(−): 19% vs MRD(+): 29% at 4 years; P=0.006). In multivariate analyses, MRD(+) at allo-HCT was a significant risk factor for relapse. A post-transplant TKI was administered to 103 patients. In subanalyses regarding the effect of post-transplant TKI administration, post-transplant TKI administration was a significant risk factor for relapse in multivariate analyses (P<0.0001). MRD status at allo-HCT is one of the most important predictive factors for Ph+ALL patients transplanted in CR1.

Abstract: Epitaxial La0.7Ca0.3MnO3 (LCMO) thin films were successfully prepared by the metal-organic deposition process on various (001) single-crystal substrates: MgO, LaAlO3 (LAO), SrTiO3 (STO), and (LaAlO3)0.3-(SrAlTaO6)0.7 (LSAT). The crystallinity and the epitaxial growth of the LCMO films were characterized by X-ray diffraction (θ − 2θ scans and pole-figure analysis). The temperature dependence of the resistance of the LCMO/LSAT, LCMO/STO and LCMO/LAO films exhibit typical characteristics with a transition from the paramagnetic-insulator state to the ferromagnetic-metallic state at a temperature peak (T p ) ranging from 258 to 270 K. However, the LCMO/MgO films exhibited a semiconducting behavior without any transition. Based on the R(T) measurement, we calculated the temperature coefficient of resistance (TCR) for a bolometric application and we obtained 22%/K, 10.2%/K and 27.5%/K for the film grown on the LSAT, STO and LAO substrates, respectively. This difference in the TCR properties is related to the strain induced by the lattice mismatch between LCMO and the different substrates.

The irradiation creep of 11Cr–0.5Mo–2W–0.2V–0.05Nb ferritic–martensitic (PNC-FMS), modified 316 (PNC316) and 15Cr–20Ni base austenitic S.S. were determined by the gas pressurized capsule irradiation test using MOTA in FFTF. The pressurized capsules and open tubes were irradiated at 678–943 K to a peak dose of 206 dpa. The irradiation creep coefficients were derived from the diametral change differences between the capsules and open tubes, accounting for the stress-induced swelling. The creep compliance B0and creep-swelling coupling coefficient Dfor PNC-FMS were found to be 0.43–0.76×10−6MPa−1dpa−1and 0.85–2.5×10−2MPa−1for volumetric swelling, respectively. For both PNC316 and 15Cr–20Ni base S.S. the irradiation creep properties were very similar. B0and Drange from 0.55 to −1.5×10−6MPa−1dpa−1and from 1.2 to −2.8×10−3MPa−1, respectively.

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YbBa2Cu4O8(Yb124) films were prepared on SrTiO3(001) and SrTiO3(110) substrates by coating-pyrolysis process at ambient pressure, and the alignments of these films were investigated by XRD θ-2θ scanning and XRD pole-figure analysis. Films prepared on SrTiO3(001) consisted of almost single-phase [001]-oriented epitaxial Yb124. On the other hand, films on SrTiO3(110) consisted of [107]-oriented epitaxial Yb124 and other impurity phases, one of which was considered to be so-called “other perovskite” phase.

Abstract: An understanding of the effects of long-term, low-dose-rate radiation on core components is critical to light-water reactor plant life extension. Following reactor shutdown, materials that had experienced long exposures to low-dose-rate irradiation were retrieved from the EBR-II research reactor for analysis. These components are being analyzed to provide insight into pressurized water reactor life extension. In this work, three examples of EBR-II materials analyses are highlighted: radiation-induced segregation in 304 stainless steel, stress relaxation in Inconel X750, and swelling in 316 stainless steel.

BaTiO3 thin films were prepared by using metal organic acid salts on MgO(100) substrates, which have large lattice-misfit with BaTiO3. Amorphous films prefired at 470°C were crystallized to BaTiO3 phase by heat treatment at higher temperature. Crystallinity and in-plane alignment of the prepared films were found to depend on the heat-treatment conditions. BaTiO3 films with high crystallinity but poor (100)-orientation were obtained in air at higher than 1200°C. Whereas, (100)-oriented epitaxial BaTiO3 film was fabricated by annealing at 900°C under low oxygen partial pressure (p(O2)). Low carbon dioxide partial pressure (p(CO2)) is also found to be essential for preparation of epitaxial BaTiO3 films on MgO substrates by using metal organic acid salts.

The stability and ordered assembly of cytoskeletal microtubules (MTs) and the relationship between cell growth and MT cytoskeleton in the coenocytic green alga, Chaetomorpha moniligera Kjellman were examined. The cytoplasm of cylindrical growing cells of Chaetomorpha is covered with dense arrays of longitudinally arranged cortical MTs which constitute the MT cytoskeleton. Seventy-five percent of MTs of the cytoskeleton disappeared within 4 h, with 25% remaining after 20 h following cold treatment. On terminating MT assembly with amiprophos-methyl (APM), the number of MTs decreased by 75% within 4 h. The remaining MTs disappeared gradually within 24 h. The MT cytoskeleton of Chaetomorpha would thus appear to be composed of at least two kinds of MTs differing in stability. The MT cytoskeleton returned to normal after treatment with APM for less than 48 h. However, this did not occur after treatment with APM for more than 48 h, and the MT arrays became random. Cell elongation ceased completely within 24 h after treatment with APM for less than 48 h but was restored within 24 h after removing APM. The restoration of cell elongation was no longer evident after removaI of APM for more than 48 h. The results indicate that assembly of MTs into ordered arrays depends on cell polarity and that in turn cell elongation is dependent on the polar-dependent arrays of MTs.Copyright 1994, 1999 Academic Press

Summary The effects of 2,6-dichlorobenzonitrile (DCB, a known inhibitor of cellulose synthesis) and Tinopal LPW (TPL, an agent which disrupts glucan crystallization) on the structure of cellulose synthesizing complexes (terminal complexes, TCs) in the xanthophycean algaVaucheria hamata were investigated. DCB (10 µM) inhibits nascent fibril formation from the TC subunit (based on the absence of impressions) although it does not alter the overall shape of the rectangular TC during the short treatment of 20 min. With a prolonged treatment (60 min), the arrangement of TC subunits becomes disordered, and particles generally exhibited as doublets of subunits are released from each other. DCB also interferes with the formation of the overall shape of the TC although it does not disturb the conversion into TC rows of the subunits (the zymogenic precursor of the TC) packed in the globules. A 15 min treatment with TPL (1 mM) destroys the TC integrity by reducing the subunits into small fragments or particulate aggregates. The particulate rows of the TC are interrupted at many points, and fragments and particulate aggregates are dispersed by prolonged treatment (45 min) with TPL. Unlike DCB, TPL inhibits the conversion of globule subunits into TC rows. New insights on the structural characteristics necessary for cellulose microfibril assembly and possible mechanisms for the biogenesis of theVaucheria TC come from these data.

Summary Ultrastructure and assembly of cellulose terminal synthesizing complexes (terminal complexes, TCs) in the algaVaucheria hamata (Waltz) were investigated by high resolution analytical techniques for freeze-fracture replication.Vaucheria TCs consist of many diagonal rows of subunits located on the inner leaflet of the plasma membrane. Each row contains about 10–18 subunits. The subunits themselves are rectangular, approx. 7×3.5 nm, and each has a single elliptical hole which may be the site of a single glucan chain polymerization. The subunits are connected with extremely small filaments (0.3–0.5 nm). Connections are more extensive in a direction parallel to the subunit rows and less extensive perpendicular to them. Nascent TC subunits are found to be packed within globules (15–20 nm in diameter) which are larger than typical intramembranous particles (IMPS are 10–11 nm in diameter) distributed in the plasma membrane. The subunits in the globule, which may be a zymogenic precursor of the TC, are generally exhibited in the form of doublets. Approximately 6 doublets are connected to a center core with small filaments. The globules are inserted into the plasma membrane together with IMPS by the fusion of cytoplasmic (Golgi derived) vesicles. Two or three globules attach to each other, unfold, and expand to form the first subunit rows of the TC on the inner leaflet of the plasma membrane. More globules attach to the structure and unfold until the nascent TC consists of a few rows of subunits. These rows are arranged almost parallel to each other. Two formation centers of subunits appear at both ends of an elongating TC. New subunits carried by the globules are added at each of these centers to create new rows until the elongating TC structure is completed. On the basis of this study, a model of TC assembly and early initiation of microfibril formation inVaucheria is proposed.

The functions of the microtubule (MT) cytoskeleton in changing the orientation of microfibrils (MFs) in the cell walls of the coenocytic green alga Chaetomorpha moniligera Kjellman were investigated by electron microscopy. The cortical MT cytoskeleton in Chaetomorpha was comprised of longitudinally oriented MTs. Cellulose MFs, however, alternately changed their orientation longitudinally and transversely to form crisscross MF textures. Microtubules were parallel to longitudinally oriented MFs but never to those that were transversely oriented. The average density of MTs during the formation of longitudinally oriented MFs was 216 per 50 µm of wall and that of transversely oriented MFs 170/50 µm. To determine exactly the MT-density dependency of each MF orientation, changes in MF orientation were examined by changing MT density after treating and removing amiprophos-methyl (APM). Microtubules were reduced in number by a half (100/50 µm) after 2 h and by 3/4 (50/50 µm) after 3 h of treatment with APM (3 mM). This reduction was caused by the disappearance of alternating MTs. Microtubules retained this density (50/ 50 µm) up to 6 h, and then gradually disappeared within 24 h. Microfibril orientation in the innermost cell wall was transverse after treatment with APM for 2 h but was helicoidal after 6 h. Polymerization of MTs occurred in the longitudinal direction following the removal of APM after treatment for 48 h. Microtubule density rose to about 100/50 µm and 200/50 µm after 6 h and 24 h, respectively. The orientation of MTs changed from helicoidal to transverse and transverse to longitudinal after 6 h and 24 h, respectively. When APM was removed prior to formation of the helicoidal texture, longitudinally oriented MFs appeared within 6 h. There is thus an alternating cycle of formation of longitudinally and transversely oriented MFs within a 12-h period. Formation of transversely oriented MFs as a result of APM treatment started in the middle of a cell as hoops which then extended in the apical and basal directions. Formation of longitudinally oriented MFs as a result of the removal of APM started from the apical end and proceeded toward the base. It follows from these results that: (1) the point of formation of longitudinally oriented MFs differs from that for transversely oriented MFs, (2) MF orientation in each case depends on a separately functioning mechanism, (3) MT density changes rhythmically to trigger a switch for crisscross orientation of MFs.

Summary The effects of 2,6-dichlorobenzonitrile (DCB, an agent which inhibits cellulose synthesis) and cycloheximide (CHI, a known inhibitor of protein synthesis) on the construction and stability of the cortical microtubule (MT) cytoskeleton in two kinds of protoplasts (smaller protoplasts and larger ones) prepared fromBoodlea coacta (Dickie) Murray et De Toni were examined by immunofluorescence microscopy. In smaller protoplasts which develop from released protoplasmic masses in culture media, parental cortical MTs assume a convoluted configuration, but new cortical MTs appear following disassembly of convoluted MTs. New cortical MTs initially have a random arrangement but later, a rough meridional arrangement following development of cell polarity and finally, a high density meridional arrangement. In larger protoplasts which are formed within cell wall cylinders of thalli cut at 500 µm length, longitudinally oriented parental cortical MTs are preserved. Each exhibits a curving configuration just after protoplast formation, but a straight configuration after 3 h of culture. In smaller protoplasts, cortical MT orientation changes from random to rough meridional orientation but never to a high density meridional orientation following treatment with 10 µM CHI, and MT density decreases after 12 h. However, rough meridional and high density meridional arrangements of MTs ceased to be formed and MT density decreased following treatment with 10 µM DCB. In larger protoplasts, high density meridional arrangements of MTs were noted not to be affected by treatment with CHI; instead, they continued to remain oriented meridionally, but the length and density were decreased after treatment with DCB for 3–4 h. After 10 h, the MTs became fragmented and orientation was random. From these findings it is summarized that: (1) There are no putative anchors in the plasma membrane of nascent smaller protoplasts, but the meridional orientation of cortical MTs requires anchors which may be distributed in the plasma membrane following the establishment of cell polarity. (2) Plasma membranes in larger protoplasts contain parental anchors oriented meridionally. Anchors stabilize cortical MTs via their close relation to cell walls (especially to cellulose). Anchors are detached from the plasma membrane when cellulose is not formed. (3) Cellulose regeneration may be indispensable to the formation and stabilization of the MT cytoskeleton inBoodlea.

Summary Examination was made of the structure and assembly of the cortical microtubule (MT) cytoskeleton in the coenocytic green algaBoodlea coacta (Dickie) Murray et De Toni by immunofluorescence microscopy. Cortical MTs inBoodlea protoplasts are arranged randomly but some show a meridional arrangement within 6 h after protoplast formation. At 6–9 h such MTs become highly concentrated and parallel to each other in certain areas. At 12 h the concentration is uniformly high throughout the cell, indicating the completion of high density meridional arrangement of cortical MTs. Cortical MTs exhibiting a high density, meridional arrangement show characteristic disassembly by treatment with 10 µM amiprophos-methyl (APM) or cold treatment (0 °C). Disassembly occurs by each MT unit at positions skipping 30–40 µm in the transverse direction, and neighboring MTs subsequently disassemble to form MT groups. Each group becomes slender and then disappears completely within the following 24 h. The meridional arrangement of cortical MTs is disrupted by N-ethylmaleimide (NEM) accompanied by a remarkable reduction in density. The remaining MTs form groups at 30–40 µm intervals from each other, as also occurs with drug or cold treatment, but disruption and density return to normal levels following removal of NEM. It appears that there are meridionally oriented channels, anchor-rich and anchor-poor, in the plasma membrane. The channels could be distributed alternately and anchors could be deposited in a cross-linking manner with cortical MTs to form a stable cortical MT-cytoskeleton. MTs comprising the cortical MT cytoskeleton could be oriented by meridionally oriented channels of anchors which are distributed following establishment of cell polarity.

Summary Microfibrillar textures and orientation of cellulose microfibrils (MFs) in the coenocytic green alga,Boergesenia forbesii, were investigated by fluorescence and electron microscopy. Newly formed aplanosporic spherical cells inBoergesenia start to form cellulose MFs on their surfaces after 2 h of culture at 25°C. Microfibrillar orientation becomes random, fountain-shaped, and helicoidal after 2, 4, and 5 h, respectively. The fountain orientation of MFs is usually apparent prior to helicoidal MF orientation and thus may be considered to initiate helicoid formation. Microfibrils continue to take on the helicoidal arrangement during the growth ofBoergesenia thallus. The helicoidal orientation of MFs occurs through gradual counterclockwise change in MF deposition by terminal complexes (TCs) viewed from inside the cell. On the dorsal side of curving TC impressions in helicoidal texture formation on a freeze-fractured plasma membrane, the aggregation of intramembranous particles (IMPs) occurs. Membrane flow may thus possibly affect the regulation of helicoidal orientation inBoergesenia. Following treatment with 3 µM amiprophos-methyl (APM) or 1 mM colchicine, cortical microtubules (MTs) completely disappear within 24 h but helicoidal textures formation is not affected. With 15 µM cytochalasin B or 30 µM phalloidin, however, the helicoidal orientation of MFs becomes random. Treatment with CaCl2 (10 mM) causes the helicoidal MF orientation of cells to become random, but co-treatment with N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide (W-7) (100 mM) prevents this effect, though W-7 has no effect on the helicoidal MF formation. It thus follows that MF orientation inBoergesenia possibly involves actin whose action may be regulated by calmodulin.

Asymmetric monobenzoylation reactions of cyclic meso-1,3- and 1,4-diols were catalyzed by a phosphinite derivative of quinidine to afford the corresponding monobenzoylated diol with good yield and enantioselectivity.

The effects of cold treatment on the cortical microtubules (MTs) of Chaetomorpha moniligera Kjellman were investigated by immunofluorescence microscopy. Cortical MTs in Chaetomorpha thallus are arranged longitudinally. In this study, 70–75% of MTs disassembled within 4 h on ice while the others remained stable under these conditions. Reticulate background immunofluorescence, assumed to indicate the presence of a tubulin monomer, was distributed about the stable MTs. Immunofluorescence was prominent in only 50% of the cells. Tubulin polymerization was noted where the background and MT immunofluorescence was strong. New MTs grew transversely as single strings or clusters from the sides of MTs after cold treatment for 4 h and elongated with time to take on a reticulate form at 24 h. The significance of this tubulin polymerization under cold treatment is discussed.