記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Wiley  

DOI： 10.1002/dvg.23509

researchmap

その他リンク： https://onlinelibrary.wiley.com/doi/full-xml/10.1002/dvg.23509

記述言語：日本語   出版者・発行元：岡山歯学会  

9年間の矯正歯科治療患者2079名(男性682名、女性1397名、平均年齢20歳1ヵ月、中央値18歳3ヵ月)を対象に、永久歯先天性欠如(先欠歯)発生率を発生部位、歯種別に検討した。その結果、先欠歯発生率は284/2079名(13.7%)で、上顎での発生率が高かった。また、口唇口蓋裂(CLCP)患者や特定疾患患者では他の患者と比較して高い先欠歯発生率を認め、CLCP患者は上顎側切歯、特定疾患患者は上顎第二大臼歯の欠如が特徴的であった。

researchmap

担当区分：責任著者   掲載種別：研究論文（学術雑誌）   出版者・発行元：Wiley  

DOI： 10.1111/pin.13168

researchmap

その他リンク： https://onlinelibrary.wiley.com/doi/full-xml/10.1111/pin.13168

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Wiley  

DOI： 10.1002/biof.1774

researchmap

その他リンク： https://onlinelibrary.wiley.com/doi/full-xml/10.1002/biof.1774

担当区分：筆頭著者,　責任著者   記述言語：日本語   掲載種別：研究論文（学術雑誌）  

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：American Association for the Advancement of Science ({AAAS})  

DOI： 10.1126/sciadv.aau7802

PubMed

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：John Wiley and Sons Inc.  

BMP signaling plays a critical role in craniofacial development. Augmentation of BMPR1A signaling through neural crest-specific expression of constitutively active Bmpr1a (caBmpr1a) results in craniofacial deformities in mice. To investigate whether deletion of Tak1 may rescue the craniofacial deformities caused by enhanced Smad-dependent signaling through caBMPR1A, we generated embryos to activate transcription of caBmpr1a transgene and ablate Tak1 in neural crest derivatives at the same time. We found that deformities of the double mutant mice showed more severe than those with each single mutation, including median facial cleft and cleft palate. We found higher levels of cell death in the medial nasal and the lateral nasal processes at E10.5 in association with higher levels of p53 in the double mutant embryos. We also found higher levels of pSmad1/5/9 in the lateral nasal processes at E10.5 in the double mutant embryos. Western analyses revealed that double mutant embryos showed similar degrees of upregulation of pSmad1/5/9 with caBmpr1a or Tak1-cKO embryos while the double mutant embryos showed higher levels of phospho-p38 than caBmpr1a or Tak1-cKO embryos at E17.5, but not at E10.5. It suggested that deletion of Tak1 aggravates the craniofacial deformities of the caBmpr1a mutants by increasing p53 and phospho-p38 at different stage of embryogenesis.

DOI： 10.1002/dvg.23093

Scopus

researchmap

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

J-GLOBAL

researchmap

DOI： 10.1177/0022034518771331

researchmap

DOI： 10.1002/dvg.23220

researchmap

掲載種別：研究論文（学術雑誌）   出版者・発行元：Springer Nature  

DOI： 10.1038/srep44522

researchmap

記述言語：日本語   出版者・発行元：岡山歯学会  

当大学の歯科矯正学分野において、「歯の移動の臨床手技実習」における60分授業・クォーター制を導入し、導入前後の年度で学生と教職員にアンケートを実施した。学生アンケートでは、導入前の平成27年度の実習受講生53名と導入後の平成28年度の受講生46名を対象とした。教職員アンケートでは、平成28年度の実習で指導にあたった教職員7名と補助した医局員20名を対象とした。その結果、導入後では実習内容、指導法、実習書といった教育コンテンツの改善により学生の自修意欲が高まり、一定の成果を上げることができていた。また、ICTを活用した授業支援システム"WebClass"も予習・復習に積極的に利用されており、成果に貢献していた。しかし、実習時間の短縮への対応の点では問題が残り、「時間不足」を訴える意見が多く聞かれた。

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ELSEVIER SCIENCE INC  

Introduction: The intercellular network of cell-cell communication among osteocytes is mediated by gap junctions. Gap junctional intercellular communication (GJIC) is thought to play an important role in the integration and synchronization of bone remodeling. To further understand the mechanism of bone development it is important to quantify the difference in the GJIC capacity of young and developmentally mature osteocytes.
Materials and methods: We first established an embryonic chick calvaria growth model to show the growth of the calvaria in embryos at 13 to 21 days of age. We then applied a fluorescence recovery after photobleaching (FRAP) technique to compare the difference in the GJIC capacity of young osteocytes with that of developmentally mature osteocytes. Finally, we quantified the dye (Calcein) diffusion from the FRAP data using a mathematic model of simple diffusion which was also used to identify simple diffusion GJIC pattern cells (fitted model) and accelerated diffusion GJIC pattern cells (non-fitted model).
Results: The relationship between the longest medial-lateral length of the calvaria (frontal bone) and the embryonic age fit a logarithmic growth model: length = 5.144 x ln(day) - 11.340. The morphometric data during osteocyte differentiation showed that the cellular body becomes more spindle-shaped and that the cell body volume decreased by approximately 22% with an increase in the length of the processes between the cells. However, there were no significant differences in the cellular body surface area or in the distance between the mass centres of the cells. The dye-displacement rate in young osteocytes was significantly higher than that in developmentally mature osteocytes: dye displacement only occurred in 26.88% of the developmentally mature osteocytes, while it occurred in 64.38% of the young osteocytes. Additionally, in all recovered osteocytes, 36% of the developmentally mature osteocytes comprised non-fitted model cells while 53.19% of the young osteocytes were the non-fitted model, which indicates the active transduction of dye molecules. However, there were no statistically significant differences between the young and developmentally mature osteocytes with regard to the diffusion coefficient, permeability coefficient, or permeance of the osteocyte processes, which were 3.93 +/- 3.77 (x 10(-8) cm(2)/s), 5.12 +/- 4.56 (x 10(-8) cm(2)/s) and 2.99 +/- 2.47 (x 10(-13) cm(2)/s) (mean SD), respectively.
Conclusions: These experiments comprehensively quantified the GJIC capacity in the embryonic chick calvaria and indicated that the cell-cell communication capacity of the osteocytes in the embryonic chick calvaria was related to their development. (C) 2016 Elsevier Inc. All rights reserved.

DOI： 10.1016/j.bone.2016.06.016

Web of Science

researchmap

記述言語：英語   出版者・発行元：ELSEVIER SCI LTD  

BMP signaling is one of the key pathways regulating craniofacial development. It is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. It regulates development of its mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. Targeted mutations in the mouse have been instrumental to delineate the functional involvement of this signaling network in different aspects of craniofacial development. Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. The identification of intricate cellular interactions and underlying molecular pathways illustrate the importance of local fine-regulation of Bmp signaling to control proliferation, apoptosis, epithelial-mesenchymal interactions, and stem/progenitor differentiation during craniofacial development. Thus, BMP signaling contributes both to shape and functionality of our facial features. BMP signaling also regulates postnatal craniofacial growth and is associated with dental structures life-long. A more detailed understanding of BMP function in growth, homeostasis, and repair of postnatal craniofacial tissues will contribute to our ability to rationally manipulate this signaling network in the context of tissue engineering. (C) 2015 Elsevier Ltd. All rights reserved.

DOI： 10.1016/j.cytogfr.2015.11.004

Web of Science

researchmap

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ACADEMIC PRESS INC ELSEVIER SCIENCE  

BMP signaling mediated by ACVR1 plays a critical role for development of multiple structures including the cardiovascular and skeletal systems. While deficient ACVR1 signaling impairs normal embryonic development, hyperactive ACVR1 function (R206H in humans and Q207D mutation in mice, ca-ACVR1) results in formation of heterotopic ossification (HO). We developed a mouse line, which conditionally expresses ca-ACVR1 with Nfatcl-Cre transgene. Mutant mice developed ectopic cartilage and bone at the distal joints of the extremities including the interphalangeal joints and hind limb ankles as early as P4 in the absence of trauma or exogenous bone morphogenetic protein (BMP) administration. Micro-CT showed that even at later time points (up to P40), cartilage and bone development persisted at the affected joints most prominently in the ankle. Interestingly, this phenotype was not present in areas of bone outside of the joints - tibia are normal in mutants and littermate controls away from the ankle. These findings demonstrate that this model may allow for further studies of heterotopic ossification, which does not require the use of stem cells, direct trauma or activation with exogenous Cre gene administration. (C) 2015 Elsevier Inc. All rights reserved.

DOI： 10.1016/j.ydbio.2015.02.011

Web of Science

researchmap

担当区分：筆頭著者   記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：COMPANY OF BIOLOGISTS LTD  

Bone morphogenetic protein (BMP) signaling plays many roles in skull morphogenesis. We have previously reported that enhanced BMP signaling through the BMP type IA receptor (BMPR1A) in cranial neural crest cells causes craniosynostosis during postnatal development. Additionally, we observed that 55% of Bmpr1a mutant mice show neonatal lethality characterized by a distended gastrointestinal tract. Here, we show that severely affected mutants exhibit defective nasal cartilage, failure of fusion between the nasal septum and the secondary palate, and higher levels of phosphorylated SMAD1 and SMAD5 in the nasal tissue. TUNEL demonstrated an increase in apoptosis in both condensing mesenchymal tissues and cartilage of the nasal region in mutants. The levels of p53 (TRP53) tumor suppressor protein were also increased in the same tissue. Injection of pifithrin-alpha, a chemical inhibitor of p53, into pregnant mice prevented neonatal lethality while concomitantly reducing apoptosis in nasal cartilage primordia, suggesting that enhanced BMP signaling induces p53-mediated apoptosis in the nasal cartilage. The expression of Bax and caspase 3, downstream targets of p53, was increased in the mutants; however, the p53 expression level was unchanged. It has been reported that MDM2 interacts with p53 to promote degradation. We found that the amount of MDM2-p53 complex was decreased in all mutants, and the most severely affected mutants had the largest decrease. Our previous finding that the BMP signaling component SMAD1 prevents MDM2-mediated p53 degradation coupled with our new data indicate that augmented BMP signaling induces p53-mediated apoptosis by prevention of p53 degradation in developing nasal cartilage. Thus, an appropriate level of BMP signaling is required for proper craniofacial morphogenesis.

DOI： 10.1242/dev.118802

Web of Science

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: The rodent salivary gland is not fully developed at birth and the cellular definitive differentiation takes place postnatally. However, little is known about its molecular mechanism. RESULTS: Here we provide the loss-of-function genetic evidence that Runx signaling affects postnatal development of the submandibular gland (SMG). Core binding factor β (Cbfb) is a cotranscription factor which forms a heterodimer with Runx proteins. Cbfb was specifically expressed in the duct epithelium, specifically in the SMG. Epithelial Cbfb deficiency resulted in decrease in the size of the SMG and in the saliva secretion on postnatal day 35. The Cbfb mutant SMG specifically exhibited involution of the granular convoluted tubules (GCT), with a down-regulated expression of its marker genes, such as Klk1, Ngf, and Egf. The induction of GCT is under the control of androgens, and the Cbfb mutant SMG demonstrated down-regulated expression of Crisp3, an androgen-dependent transcript. Because the circulating testosterone or tissue dihydrotestosterone levels were not affected in the Cbfb mutants, it appears that Runx/Cbfb signaling regulate androgen receptor pathway, but does not affect the circulating testosterone levels or the enzymatic conversion to DHT. CONCLUSIONS: Runx signaling is important in the postnatal development of androgen-dependent GCT in the SMG.

DOI： 10.1002/dvdy.24231

PubMed

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：PUBLIC LIBRARY SCIENCE  

We herein describe a novel procedure for dentin regeneration that mimics the biological processes of tooth development in nature. The canonical Wnt signaling pathway is an important regulator of the Dentin sialophosphoprotein (Dspp) expression. Our approach mimics the biological processes underlying tooth development in nature and focuses on the activation of canonical Wnt signaling to trigger the natural process of dentinogenesis. The coronal portion of the dentin and the underlying pulp was removed from the first molars. We applied lithium chloride (LiCl), an activator of canonical Wnt signaling, on the amputated pulp surface to achieve transdifferentiation toward odontoblasts from the surrounding pulpal cells. MicroCT and microscopic analyses demonstrated that the topical application of LiCl induced dentin repair, including the formation of a complete dentin bridge. LiCl-induced dentin is a tubular dentin in which the pulp cells are not embedded within the matrix, as in primary dentin. In contrast, a dentin bridge was not induced in the control group treated with pulp capping with material carriers alone, although osteodentin without tubular formation was induced at a comparatively deeper position from the pulp exposure site. We also evaluated the influence of LiCl on differentiation toward odontoblasts in vitro. In the mDP odontoblast cell line, LiCl activated the mRNA expression of Dspp, Axin2 and Kallikrein 4 (Klk4) and downregulated the Osteopontin (Osp) expression. These results provide a scientific basis for the biomimetic regeneration of dentin using LiCl as a new capping material to activate dentine regeneration.

DOI： 10.1371/journal.pone.0121938

Web of Science

researchmap

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ELSEVIER SCIENCE INC  

Bone cells respond to mechanical stimuli by producing a variety of biological signals, and one of the earliest events is intracellular calcium ([Ca2+](i)) mobilization. Our recently developed ex vivo live [Ca2+](i) imaging system revealed that bone cells in intact bone explants showed autonomous [Ca2+](i) oscillations, and osteocytes specifically modulated these oscillations through gap junctions. However, the behavior and connectivity of the [Ca2+](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 [Ca2+](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 alpha-GA, a reversible inhibitor of gap junction, significantly blocked the [Ca2+](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 Gd3+, is less affected in the flow-induced [Ca2+](i) response. These findings indicated that flow-induced mechanical stimuli accompanied the activation of the autonomous [Ca2+](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 [Ca2+](i) mobilization could be involved as an early signaling event in mechanotransduction. (C) 2012 Elsevier Inc. All rights reserved.

DOI： 10.1016/j.bone.2012.12.002

Web of Science

researchmap

記述言語：日本語   出版者・発行元：中・四国矯正歯科学会  

researchmap

記述言語：日本語   出版者・発行元：(NPO)日本顎変形症学会  

researchmap

掲載種別：研究論文（学術雑誌）  

DOI： 10.1002/stem.722

Scopus

PubMed

researchmap

記述言語：日本語   出版者・発行元：(公社)日本矯正歯科学会  

researchmap

記述言語：日本語   出版者・発行元：(公社)日本矯正歯科学会  

researchmap

記述言語：日本語   出版者・発行元：(公社)日本矯正歯科学会  

researchmap

掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.diff.2009.10.005

Scopus

PubMed

researchmap

記述言語：日本語   出版者・発行元：(一社)歯科基礎医学会  

researchmap

記述言語：日本語   出版者・発行元：日本組織培養学会  

researchmap

記述言語：日本語   出版者・発行元：日本組織培養学会  

DOI： 10.11418/jtca.29.111

researchmap

記述言語：日本語   出版者・発行元：(公社)日本矯正歯科学会  

researchmap

記述言語：日本語   出版者・発行元：(公社)日本矯正歯科学会  

researchmap

開催年月日： 2022年10月5日 - 2022年10月7日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2022年10月5日 - 2022年10月7日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2022年10月5日 - 2022年10月7日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2022年6月30日 - 2022年7月2日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2022年6月9日 - 2022年6月10日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2022年5月26日 - 2022年5月27日

記述言語：英語   会議種別：口頭発表（一般）  

researchmap

開催年月日： 2021年8月7日 - 2022年8月8日

記述言語：日本語   会議種別：口頭発表（一般）  

researchmap

開催年月日： 2020年10月4日 - 2020年10月7日

記述言語：英語   会議種別：ポスター発表  

researchmap

開催年月日： 2020年7月4日 - 2020年7月5日

記述言語：日本語   会議種別：ポスター発表  

researchmap

開催年月日： 2019年11月20日 - 2019年11月22日

記述言語：英語   会議種別：ポスター発表  

researchmap

開催年月日： 2019年6月19日 - 2019年6月22日

記述言語：英語   会議種別：ポスター発表  

開催地：Vancouver, BC, Canada  

researchmap

開催年月日： 2019年6月17日 - 2019年6月22日

記述言語：英語   会議種別：ポスター発表  

researchmap

開催年月日： 2018年6月17日 - 2018年6月22日

記述言語：英語   会議種別：ポスター発表  

開催地：Edinburgh, U.K.  

researchmap

開催年月日： 2016年11月7日 - 2016年11月9日

記述言語：日本語   会議種別：ポスター発表  

開催地：徳島市あわぎんホール  

researchmap

開催年月日： 2014年2月3日

記述言語：日本語   会議種別：口頭発表（招待・特別）  

開催地：〒649-6493和歌山県紀の川市西三谷930 近畿大学大学院生物理工学研究科  

researchmap

researchmap