206 research outputs found

    BIOMECHANICAL STUDY ON DIFFERENT DIRECTIONS FOR RUNNING JUMPS FOCUSED ON THE TAKEOFF PREPARATION

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    This study aimed to elucidate the difference in CG parameters from three steps, prejump to takeoff step of the jump motion (running jump), and obtain primary data on takeoff preparation action. Five male jumpers associated with the university track and field department were trained to perform their best at (1) approach run with no takeoff (RUN), (2) jumping as far as possible (long jump [LJ]), and (3) jumping as high as possible (high jump [HJ]), which were recorded using a three-dimensional capture system. As a result, significant differences were observed in not only the takeoff but also the takeoff preparation phase regarding CG parameters, suggesting the need to focus on the takeoff preparation phase as a factor that determines jump direction. Moreover, HJ and LJ suppressed an increase in vertical velocity one step prior, and by takeoff at a lower CG, the athletes allowed for an easier increase in takeoff angle and jump height. However, to resist a decrease in horizontal velocity, LJ transitioned to takeoff in a manner closer to RUN and without changing takeoff preparation as much as that in HJ. Thus, adjusting vertical velocity and height one step before takeoff can influence takeoff angle

    Protocol for making an animal model of “blindsight” in macaque monkeys

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    Patients with damage to the primary visual cortex (V1) can respond correctly to visual stimuli in their lesion-affected visual field above the chance level, an ability named blindsight. Here, we present a protocol for making an animal model of blindsight in macaque monkeys. We describe the steps to perform pre-lesion training of monkeys on a visual task, followed by lesion surgery, post-lesion training, and evaluation of blindsight. This animal model can be used to investigate the source of visual awareness. For complete details on the use and execution of this protocol, please refer to Yoshida et al. (2008)1 and Takakuwa et al. (2021)

    Local lattice instability and stripes in the CuO 2 plane of the La 1.85 Sr 0.15 CuO 4 system by polarized XANES and EXAFS

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    Temperature-dependent polarized Cu K-edge x-ray absorption has been used to investigate local structural distortions in the CuO2{\mathrm{CuO}}_{2} plane of the La1.85{\mathrm{La}}_{1.85}Sr0.15{\mathrm{Sr}}_{0.15}CuO4{\mathrm{CuO}}_{4} system. The Cu-O pair distribution shows the presence of a minority phase containing CuO6{\mathrm{CuO}}_{6} octahedra characterized by a shorter Cu-O(apical) bond (\ensuremath{\Delta}R\ensuremath{\sim}-0.1 \AA{}) and two longer Cu-O(planar) bonds (\ensuremath{\Delta}R\ensuremath{\sim}+0.08 \AA{}) and a tilting angle of 16\ifmmode^\circ\else\textdegree\fi{}\ifmmode\pm\else\textpm\fi{}2\ifmmode^\circ\else\textdegree\fi{}. The temperature-dependent distortions show a maximum around T (\ensuremath{\sim}1.6Tc{6\mathrm{T}}_{\mathrm{c}}) and a minimum at Tc{\mathrm{T}}_{\mathrm{c}} (\ensuremath{\sim}35 K). The data show the coexistence of two types of doped charges in different stripes in the superconducting phase

    Culture temperature affects human chondrocyte messenger RNA expression in monolayer and pellet culture systems

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    Cell-based therapy has been explored for articular cartilage regeneration. Autologous chondrocyte implantation is a promising cell-based technique for repairing articular cartilage defects. However, there are several issues such as chondrocyte de-differentiation. While numerous studies have been designed to overcome some of these issues, only a few have focused on the thermal environment that can affect chondrocyte metabolism and phenotype. In this study, the effects of different culture temperatures on human chondrocyte metabolism- and phenotype-related gene expression were investigated in 2D and 3D environments. Human chondrocytes were cultured in a monolayer or in a pellet culture system at three different culture temperatures (32° C, 37° C, and 41° C) for 3 days. The results showed that the total RNA level, normalized to the threshold cycle value of internal reference genes, was higher at lower temperatures in both culture systems. Glyceraldehyde-3- phosphate dehydrogenase (GAPDH) and citrate synthase (CS), which are involved in glycolysis and the citric acid cycle, respectively, were expressed at similar levels at 32° C and 37° C in pellet cultures, but the levels were significantly lower at 41° C. Expression of the chondrogenic markers, collagen type IIA1 (COL2A1) and aggrecan (ACAN), was higher at 37° C than at 32° C and 41° C in both culture systems. However, this phenomenon did not coincide with SRY (sex-determining region Y)-box 9 (SOX9), which is a fundamental transcription factor for chondrogenesis, indicating that a SOX9-independent pathway might be involved in this phenomenon. In conclusion, the expression of chondrocyte metabolism-related genes at 32° C was maintained or enhanced compared to that at 37° C. However, chondrogenesis-related genes were further induced at 37° C in both culture systems. Therefore, manipulating the culture temperature may be an advantageous approach for regulating human chondrocyte metabolic activity and chondrogenesis

    Immature articular cartilage and subchondral bone covered by menisci are potentially susceptive to mechanical load

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    BACKGROUND: The differences of mechanical and histological properties between cartilage covered by menisci and uncovered by menisci may contribute to the osteoarthritis after meniscectomy and these differences are not fully understood. The purpose of this study is to investigate potential differences in the mechanical and histological properties, and in particular the collagen architecture, of the superficial cartilage layer and subchondral bone between regions covered and uncovered by menisci using immature knee. METHODS: Osteochondral plugs were obtained from porcine tibial cartilage that was either covered or uncovered by menisci. Investigation of the thickness, mechanical properties, histology, and water content of the cartilage as well as micro-computed tomography analysis of the subchondral bone was performed to compare these regions. Collagen architecture was also assessed by using scanning electron microscopy. RESULTS: Compared to the cartilage uncovered by menisci, that covered by menisci was thinner and showed a higher deformity to compression loading and higher water content. In the superficial layer of cartilage in the uncovered regions, collagen fibers showed high density, whereas they showed low density in covered regions. Furthermore, subchondral bone architecture varied between the 2 regions, and showed low bone density in covered regions. CONCLUSIONS: Cartilage covered by menisci differed from that uncovered in both its mechanical and histological properties, especially with regards to the density of the superficial collagen layer. These regional differences may be related to local mechanical environment in normal condition and indicate that cartilage covered by menisci is tightly guarded by menisci from extreme mechanical loading. Our results indicate that immature cartilage degeneration and subchondral microfracture may occur easily to extreme direct mechanical loading in covered region after meniscectomy

    Contributions of biarticular myogenic components to the limitation of the range of motion after immobilization of rat knee joint

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    BACKGROUND: Muscle atrophy caused by immobilization in the shortened position is characterized by a decrease in the size or cross-sectional area (CSA) of myofibers and decreased muscle length. Few studies have addressed the relationship between limitation of the range of motion (ROM) and the changes in CSA specifically in biarticular muscles after atrophy because of immobilization. We aimed to determine the contribution of 2 distinct muscle groups, the biarticular muscles of the post thigh (PT) and those of the post leg (PL), to the limitation of ROM as well as changes in the myofiber CSAs after joint immobilization surgery. METHODS: Male Wistar rats (n = 40) were randomly divided into experimental and control groups. In the experimental group, the left knee was surgically immobilized by external fixation for 1, 2, 4, 8, or 16 weeks (n = 5 each) and sham surgery was performed on the right knee. The rats in the control groups (n = 3 per time point) did not undergo surgery. After the indicated immobilization periods, myotomy of the PT or PL biarticular muscles was performed and the ROM was measured. The hamstrings and gastrocnemius muscles from the animals operated for 1 or 16 weeks were subjected to morphological analysis. RESULTS: In immobilized knees, the relative contribution of the PT biarticular myogenic components to the total restriction reached 80% throughout the first 4 weeks and decreased thereafter. The relative contribution of the PL biarticular myogenic components remained <20% throughout the immobilization period. The ratio of the myofiber CSA of the immobilized to that of the sham-operated knees was significantly lower at 16 weeks after surgery than at 1 week after surgery only in the hamstrings. CONCLUSIONS: The relative contribution of the PT and PL components to myogenic contracture did not significantly change during the experimental period. However, the ratio of hamstrings CSAs to the sham side was larger than the ratio of medial gastrocnemius CSAs to the sham side after complete atrophy because of immobilization

    The Effect of Exercise on the Early Stages of Mesenchymal Stromal Cell-Induced Cartilage Repair in a Rat Osteochondral Defect Model

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    The repair of articular cartilage is challenging owing to the restriction in the ability of articular cartilage to repair itself. Therefore, cell supplementation therapy is possible cartilage repair method. However, few studies have verified the efficacy and safety of cell supplementation therapy. The current study assessed the effect of exercise on early the phase of cartilage repair following cell supplementation utilizing mesenchymal stromal cell (MSC) intra-articular injection. An osteochondral defect was created on the femoral grooves bilaterally of Wistar rats. Mesenchymal stromal cells that were obtained from male Wistar rats were cultured in monolayer. After 4 weeks, MSCs were injected into the right knee joint and the rats were randomized into an exercise or no-exercise intervention group. The femurs were divided as follows: C group (no exercise without MSC injection); E group (exercise without MSC injection); M group (no exercise with MSC injection); and ME group (exercise with MSC injection). At 2, 4, and 8 weeks after the injection, the femurs were sectioned and histologically graded using the Wakitani cartilage repair scoring system. At 2 weeks after the injection, the total histological scores of the M and ME groups improved significantly compared with those of the C group. Four weeks after the injection, the scores of both the M and ME groups improved significantly. Additionally, the scores in the ME group showed a significant improvement compared to those in the M group. The improvement in the scores of the E, M, and ME groups at 8 weeks were not significantly different. The findings indicate that exercise may enhance cartilage repair after an MSC intra-articular injection. This study highlights the importance of exercise following cell transplantation therapy

    The effects of short-term hypoxia on human mesenchymal stem cell proliferation, viability and p16(INK4A) mRNA expression: Investigation using a simple hypoxic culture system with a deoxidizing agent

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    A hypoxic environment is thought to be important for the maintenance of stemness and suppressing cell senescence, in stem cells. Therefore, a hypoxic condition is induced during cell expansion and/or induction of intended differentiation. However, the induction of these conditions requires a specially equipped hypoxia chamber and expensive gas mixtures, which are expensive and space-consuming. Owing to these restrictions, appropriate hypoxic conditions cannot be provided during cell transportation, which is increasingly required for regenerative medicine. Hence, a simple and economical culture system is required. The purpose of this study was to investigate the effects of short-term hypoxic conditions on human mesenchymal stem cell (MSC) proliferation, viability, and senescence, utilizing the CulturePal system (CulturePal-Zero and CulturePal-Five), a novel and simple hypoxic culture system with a built-in deoxidizing agent. The O₂ concentration in the CulturePal-Zero was observed to reduce to <0.1% within 1 h, and to 5% within 24 h in the CulturePal-Five system. Cell proliferation under these hypoxic conditions showed a sharp increase at 5% O₂ concentration, and no noticeable cell death was observed even at severe hypoxic conditions (<0.1% O₂) up to 72h. The p16INK4A (cell senescence marker) mRNA expression was retained under hypoxic conditions up to 72h, but it was up-regulated under normoxic conditions. Interestingly, the p16INK4A expression altered proportionately to the O₂ concentration. These results indicated that the short-term hypoxic condition, at an approximate O₂ concentration of 5%, would be suitable for promoting cell proliferation and repressing cell senescence, without aggravating the MSC viability. Therefore, the CulturePal systems may be suitable for providing an appropriate hypoxic condition in stem cell research and transportation

    Three-dimensional imaging of crack growth in L chondrites after high-velocity impact experiments

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    Small asteroids such as Itokawa are covered with an unconsolidated regolith layer of centimeter-sized or smaller particles. There are two plausible formation mechanisms for regolith layers on a sub-kilometer-sized asteroid: (i) fragments produced by thermal fatigue by day-night temperature cycles on the asteroid surface and (ii) impact fragment. Previous studies suggest that thermal fatigue induces crack growth along the boundary surface of the mineral grain while impact phenomena may induce crack growth regardless of the boundary surface of the mineral grain. Therefore, it is possible that the crack growth within a mineral grain (and/or a chondrule) differs depending on the crack formation mechanism, be it thermal fatigue or an impact. In order to investigate how mineral grains and chondrules are affected by impact-induced crack growth, we fired spherical alumina projectiles (diameter ~1 mm) into 9 mm side length cubic targets of L chondrites at a nominal impact velocity of 2.0 km/s. Before and after the six successful impact experiments, the cracks within mineral grains and chondrules in the respective targets are examined using X-ray microtomography at a resolution with the voxel size of 9.0 μm. The results show that most cracks within chondrules and troilite (FeS) grow regardless of the boundary surfaces of the grains while most cracks within ductile Fe-Ni metal grow along the boundary surfaces of the grains. This may indicate that crack growth is largely affected by the strength of mineral grains (and/or chondrules). From the experimental results and the fact that the shapes of polymineralic and monomineralic particles from Itokawa are similar, we conclude that the Itokawa particles have not been produced by thermal fatigue but instead are likely to be impact fragments, as described in previous papers (Tsuchiyama et al., 2011, 2014; Michikami et al., 2018)

    NKX2-1/TITF1/TTF-1-Induced ROR1 Is Required to Sustain EGFR Survival Signaling in Lung Adenocarcinoma

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    SummaryWe and others previously identified NKX2-1, also known as TITF1 and TTF-1, as a lineage-survival oncogene in lung adenocarcinomas. Here we show that NKX2-1 induces the expression of the receptor tyrosine kinase-like orphan receptor 1 (ROR1), which in turn sustains a favorable balance between prosurvival PI3K-AKT and pro-apoptotic p38 signaling, in part through ROR1 kinase-dependent c-Src activation, as well as kinase activity-independent sustainment of the EGFR-ERBB3 association, ERBB3 phosphorylation, and consequential PI3K activation. Notably, ROR1 knockdown effectively inhibited lung adenocarcinoma cell lines, irrespective of their EGFR status, including those with resistance to the EGFR tyrosine kinase inhibitor gefitinib. Our findings thus identify ROR1 as an “Achilles' heel” in lung adenocarcinoma, warranting future development of therapeutic strategies for this devastating cancer
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