8 results on '"Yamashiro, T."'
Search Results
2. Inferior alveolar nerve transection inhibits increase in osteoclast appearance during experimental tooth movement
- Author
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Yamashiro, T, Fujiyama, K, Fujiyoshi, Y, Inaguma, N, and Takano-Yamamoto, T
- Published
- 2000
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3. CCN2/CTGF has anti-aging effects to protect articular cartilage from age-related degenerative changes
- Author
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Itoh, S., primary, Hattori, T., additional, Tomita, N., additional, Aoyama, E., additional, Yamashiro, T., additional, and Takigawa, M., additional
- Published
- 2009
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4. Ex vivo real-time observation of Ca(2+) signaling in living bone in response to shear stress applied on the bone surface.
- Author
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Ishihara Y, Sugawara Y, Kamioka H, Kawanabe N, Hayano S, Balam TA, Naruse K, and Yamashiro T
- Subjects
- Animals, Base Sequence, Chick Embryo, DNA Primers, Genes, fos, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Bone and Bones metabolism, Calcium Signaling, Stress, Psychological
- Abstract
Bone cells respond to mechanical stimuli by producing a variety of biological signals, and one of the earliest events is intracellular calcium ([Ca(2+)](i)) mobilization. Our recently developed ex vivo live [Ca(2+)](i) imaging system revealed that bone cells in intact bone explants showed autonomous [Ca(2+)](i) oscillations, and osteocytes specifically modulated these oscillations through gap junctions. However, the behavior and connectivity of the [Ca(2+)](i) signaling networks in mechanotransduction have not been investigated in intact bone. We herein introduce a novel fluid-flow platform for probing cellular signaling networks in live intact bone, which allows the application of capillary-driven flow just on the bone explant surface while performing real-time fluorogenic monitoring of the [Ca(2+)](i) changes. In response to the flow, the percentage of responsive cells was increased in both osteoblasts and osteocytes, together with upregulation of c-fos expression in the explants. However, enhancement of the peak relative fluorescence intensity was not evident. Treatment with 18 α-GA, a reversible inhibitor of gap junction, significantly blocked the [Ca(2+)](i) responsiveness in osteocytes without exerting any major effect in osteoblasts. On the contrary, such treatment significantly decreased the flow-activated oscillatory response frequency in both osteoblasts and osteocytes. The stretch-activated membrane channel, when blocked by Gd(3+), is less affected in the flow-induced [Ca(2+)](i) response. These findings indicated that flow-induced mechanical stimuli accompanied the activation of the autonomous [Ca(2+)](i) oscillations in both osteoblasts and osteocytes via gap junction-mediated cell-cell communication and hemichannel. Although how the bone sense the mechanical stimuli in vivo still needs to be elucidated, the present study suggests that cell-cell signaling via augmented gap junction and hemichannel-mediated [Ca(2+)](i) mobilization could be involved as an early signaling event in mechanotransduction., (Copyright © 2012 Elsevier Inc. All rights reserved.)
- Published
- 2013
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5. The early mouse 3D osteocyte network in the presence and absence of mechanical loading.
- Author
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Sugawara Y, Kamioka H, Ishihara Y, Fujisawa N, Kawanabe N, and Yamashiro T
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- Animals, Biomechanical Phenomena, Female, Mice, Mice, Inbred C57BL, Pregnancy, Osteocytes cytology
- Abstract
Osteocytes are considered to act as mechanosensory cells in bone. They form a functional synctia in which their processes become interconnected to constitute a three-dimensional (3D) network. Previous studies reported that in mice, the two-dimensional osteocyte network becomes progressively more regular as they grow, although the key factors governing the arrangement of the osteocyte network during bone growth remain unknown. In this study, we characterized the 3D formation of the osteocyte network during bone growth. Morphological skeletal changes have been reported to occur in response to mechanical loading and unloading. In order to evaluate the effect of mechanical unloading on osteocyte network formation, we subjected newborn mice to sciatic neurectomy in order to immobilize their left hind limb as an unloading model. The osteocyte network was visualized by staining osteocyte cell bodies and processes with fluorescently labeled phalloidin. First, we compared the osteocyte network in the femora of embryonic and 6-week-old mice in order to understand the morphological changes that occur with normal growth and mechanical loading. In embryonic mice, the osteocyte network in the femur cortical bone displayed a random cell body distribution, non-directional orientation of cell processes, and irregularly shaped cells. In 6-week-old mice, the 3D network contained spindle-shaped osteocytes, which were arranged parallel to the longitudinal axis of the femur. In addition, more and longer cell processes radiated from each osteocyte. Second, we compared the cortical osteocyte networks of 6-week-old mice that had or had not undergone sciatic neurectomy in order to evaluate the effect of unloading on osteocyte network formation. The osteocyte network formation in both cortical bone and cancellous bone was affected by mechanical loading. However, there were differences in the extent of network formation between cortical bone and cancellous bone in response to mechanical loading with regard to the orientation, nuclear shape and branch formation., (Copyright © 2012 Elsevier Inc. All rights reserved.)
- Published
- 2013
- Full Text
- View/download PDF
6. In situ imaging of the autonomous intracellular Ca(2+) oscillations of osteoblasts and osteocytes in bone.
- Author
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Ishihara Y, Sugawara Y, Kamioka H, Kawanabe N, Kurosaka H, Naruse K, and Yamashiro T
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- Animals, Chickens, Collagenases pharmacology, Endoplasmic Reticulum drug effects, Endoplasmic Reticulum metabolism, Fluorescent Dyes metabolism, Gap Junctions drug effects, Gap Junctions metabolism, Intracellular Space drug effects, Microscopy, Confocal, Osteoblasts cytology, Osteoblasts drug effects, Osteoblasts ultrastructure, Osteocytes cytology, Osteocytes drug effects, Osteocytes ultrastructure, Skull cytology, Skull ultrastructure, Time-Lapse Imaging, Bone and Bones cytology, Bone and Bones metabolism, Calcium Signaling drug effects, Imaging, Three-Dimensional methods, Intracellular Space metabolism, Osteoblasts metabolism, Osteocytes metabolism
- Abstract
Bone cells form a complex three-dimensional network consisting of osteoblasts and osteocytes embedded in a mineralized extracellular matrix. Ca(2+) acts as a ubiquitous secondary messenger in various physiological cellular processes and transduces numerous signals to the cell interior and between cells. However, the intracellular Ca(2+) dynamics of bone cells have not been evaluated in living bone. In the present study, we developed a novel ex-vivo live Ca(2+) imaging system that allows the dynamic intracellular Ca(2+) concentration ([Ca(2+)](i)) responses of intact chick calvaria explants to be observed without damaging the bone network. Our live imaging analysis revealed for the first time that both osteoblasts and osteocytes display repetitive and autonomic [Ca(2+)](i) oscillations ex vivo. Thapsigargin, an inhibitor of the endoplasmic reticulum that induces the emptying of intracellular Ca(2+) stores, abolished these [Ca(2+)](i) responses in both osteoblasts and osteocytes, indicating that Ca(2+) release from intracellular stores plays a key role in the [Ca(2+)](i) oscillations of these bone cells in intact bone explants. Another possible [Ca(2+)](i) transient system to be considered is gap junctional communication through which Ca(2+) and other messenger molecules move, at least in part, across cell-cell junctions; therefore, we also investigated the role of gap junctions in the maintenance of the autonomic [Ca(2+)](i) oscillations observed in the intact bone. Treatment with three distinct gap junction inhibitors, 18α-glycyrrhetinic acid, oleamide, and octanol, significantly reduced the proportion of responsive osteocytes, indicating that gap junctions are important for the maintenance of [Ca(2+)](i) oscillations in osteocytes, but less in osteoblasts. Taken together, we found that the bone cells in intact bone explants showed autonomous [Ca(2+)](i) oscillations that required the release of intracellular Ca(2+) stores. In addition, osteocytes specifically modulated these oscillations via cell-cell communication through gap junctions, which maintains the observed [Ca(2+)](i) oscillations of bone cells., (Copyright © 2012 Elsevier Inc. All rights reserved.)
- Published
- 2012
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7. The alteration of a mechanical property of bone cells during the process of changing from osteoblasts to osteocytes.
- Author
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Sugawara Y, Ando R, Kamioka H, Ishihara Y, Murshid SA, Hashimoto K, Kataoka N, Tsujioka K, Kajiya F, Yamashiro T, and Takano-Yamamoto T
- Subjects
- Animals, Chick Embryo, Microscopy, Confocal, Oligopeptides pharmacology, Cell Lineage, Osteoblasts cytology, Osteocytes cytology
- Abstract
Osteocytes acquire their stellate shape during the process of changing from osteoblasts in bone. Throughout this process, dynamic cytoskeletal changes occur. In general, changes of the cytoskeleton affect cellular mechanical properties. Mechanical properties of living cells are connected with their biological functions and physiological processes. In this study, we for the first time analyzed elastic modulus, a mechanical property of bone cells. Bone cells in embryonic chick calvariae and in isolated culture were identified using fluorescently labeled phalloidin and OB7.3, a chick osteocyte-specific monoclonal antibody, and then observed by confocal laser scanning microscopy. The elastic modulus of living cells was analyzed with atomic force microscopy. To examine the consequences of focal adhesion formation on the elastic modulus, cells were pretreated with GRGDS and GRGES, and then the elastic modulus of the cells was analyzed. Focal adhesions in the cells were visualized by immunofluorescence of vinculin. From fluorescence images, we could distinguish osteoblasts, osteoid osteocytes and mature osteocytes both in vivo and in vitro. The elastic modulus of peripheral regions of cells in all three populations was significantly higher than in their nuclear regions. The elastic modulus of the peripheral region of osteoblasts was 12053+/-934 Pa, that of osteoid osteocytes was 7971+/-422 Pa and that of mature osteocytes was 4471+/-198 Pa. These results suggest that the level of elastic modulus of bone cells was proportional to the stage of changing from osteoblasts to osteocytes. The focal adhesion area of osteoblasts was significantly higher than that of osteocytes. The focal adhesion area of osteoblasts was decreased after treatment with GRGDS, however, that of osteocytes was not. The elastic modulus of osteoblasts and osteoid osteocytes were decreased after treatment with GRGDS. However, that of mature osteocytes was not changed. There were dynamic changes in the mechanical property of elastic modulus and in focal adhesions of bone cells.
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- 2008
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8. Connective tissue growth factor mRNA expression pattern in cartilages is associated with their type I collagen expression.
- Author
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Fukunaga T, Yamashiro T, Oya S, Takeshita N, Takigawa M, and Takano-Yamamoto T
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- Animals, Bone Regeneration physiology, Bony Callus anatomy & histology, Bony Callus cytology, Bony Callus metabolism, Cartilage chemistry, Cartilage cytology, Cartilage, Articular chemistry, Cartilage, Articular cytology, Cartilage, Articular metabolism, Cell Differentiation physiology, Chondrocytes chemistry, Chondrocytes cytology, Chondrocytes metabolism, Collagen Type II genetics, Collagen Type X genetics, Connective Tissue Growth Factor, Femur chemistry, Femur cytology, Femur metabolism, Fracture Healing physiology, Gene Expression, Growth Plate chemistry, Growth Plate cytology, Growth Plate metabolism, Immediate-Early Proteins analysis, Immunohistochemistry, In Situ Hybridization, Intercellular Signaling Peptides and Proteins analysis, Male, Mandible chemistry, Mandible cytology, Mandible pathology, Mandibular Condyle chemistry, Mandibular Condyle cytology, Mandibular Condyle metabolism, Mandibular Injuries metabolism, Mandibular Injuries pathology, RNA, Messenger genetics, Rats, Rats, Wistar, Cartilage metabolism, Collagen Type I genetics, Gene Expression Profiling, Immediate-Early Proteins genetics, Intercellular Signaling Peptides and Proteins genetics, RNA, Messenger metabolism
- Abstract
Connective tissue growth factor (CTGF) has been identified as a secretory protein encoded by an immediate early gene and is a member of the CCN family. In vitro CTGF directly regulates the proliferation and differentiation of chondrocytes; however, a previous study showed that it was localized only in the hypertrophic chondrocytes in the costal cartilages of E 18 mouse embryos. We described the expression of CTGF mRNA and protein in chondrocytes of different types of cartilages, including femoral growth plate cartilage, costal cartilage, femoral articular cartilage, mandibular condylar cartilage, and cartilage formed during the healing of mandibular ramus fractures revealed by in situ hybridization and immunohistochemistry. To characterize the CTGF-expressing cells, we also analyzed the distribution of the type I, type II, and type X collagen mRNA expression. Among these different types of cartilages we found distinct patterns of CTGF mRNA and protein expression. Growth plate cartilage and the costal cartilage showed localization of CTGF mRNA and protein in the hypertrophic chondrocytes that expressed type X collagen mRNA with less expression in proliferating chondrocytes that expressed type II collagen mRNA, whereas it was also expressed in the proliferating chondrocytes that expressed type I collagen mRNA in the condylar cartilage, the articular cartilage, and the cartilage appearing during fracture healing. In contrast, the growth plate cartilages or the costal cartilages were negative for type I collagen and showed sparse expression of CTGF mRNA in the proliferating chondrocytes. We found for the first time that CTGF mRNA could be differentially expressed in five different types of cartilage associated with those expressing type I collagen. Moreover, the spatial distribution of CTGF mRNA in the cartilages with type I collagen mRNA suggested its roles in the early differentiation, as well as in the proliferation and the terminal differentiation, of those cartilages.
- Published
- 2003
- Full Text
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