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Bulletin du Groupement international pour la recherche scientifique en stomatologie & odontologie最新文献

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O34-pathogen sensing by human odontoblasts. 人成牙细胞o34病原感知。
J-C Fargues, J-F Keller, F Carrouel, T A Kufer, C Baudouin, P Msika, F Bleicher, M-J Staquet

Human odontoblasts are neural crest-derived, dentin-producing mesenchymal cells aligned at the periphery of the dental pulp. They become exposed to cariogenic oral bacteria as these progressively demineralise enamel then dentin to gain access to the pulp. Due to their situation at the dentin-pulp interface, odontoblasts are the first cells encountered by invading pathogens and/or their released components, and represent, in the tooth, the first line of defence for the host. Previous studies have shown that odontoblasts are able to sense pathogens and elicit innate immunity. In particular, they express several pathogen recognition receptors of the Toll-like receptor (TLR) and nucleotide-binding oligomerisation domain (NOD) families, which allow them to recognize specific bacterial and viral components. So far, most studies aiming at elucidating the role of odontoblasts in the dental pulp innate response have focused on Gram-positive bacteria, as these largely dominate the carious microflora in initial and moderate dentin caries lesions. In vitro, odontoblasts were found to be sensitive to Gram-positive bacteria-derived components, mainly lipoteichoic acid which is recognized through cell membrane TLR2. Our studies have shown that engagement of odontoblast TLR2 by LTA triggers TLR2 and NOD2 up-regulation, NF-B nuclear translocation, production of various chemokines including CCL2, CXCL1, CXCL2, CXCL8 and CXCL10, while promoting immature dendritic cell recruitment. Conversely, LTA down-regulates major dentin matrix components, including collagen type I and dentin sialophosphoprotein, as well as TGF-b1, a known inducer of dentin formation. We provide here additional data showing the fine localization of NOD2 in healthy dental pulps, as well as differential regulation of TLR2, TLR4, NOD2, CCL2 and CXCL8 genes by LTA and the synthetic TLR2 agonists Pam2CSK4 and Pam3CSK4. It appears from the aforementioned data that odontoblast-triggered immune events constitute potential targets for interrupting the signaling cascades which lead to excessive immune response and necrosis in the dental pulp tissue challenged with cariogenic bacteria. In particular, preventing Gram-positive bacteria recognition or signal transduction by pattern recognition receptors may represent a valuable strategy to achieve this goal. Future studies in the field will pave the way for designing novel therapeutic agents which modulate odontoblast behaviour to promote pulp healing and repair.

人成牙细胞是神经嵴衍生的,牙本质产生的间充质细胞排列在牙髓的外围。当这些细菌逐渐使牙釉质和牙本质脱矿,从而进入牙髓时,他们就会接触到致龋口腔细菌。由于它们位于牙本质-牙髓界面,成牙细胞是入侵病原体和/或其释放的成分遇到的第一个细胞,并且在牙齿中代表宿主的第一道防线。先前的研究表明,成牙细胞能够感知病原体并引发先天免疫。特别是,它们表达toll样受体(TLR)和核苷酸结合寡聚化结构域(NOD)家族的几种病原体识别受体,这使它们能够识别特定的细菌和病毒成分。到目前为止,大多数旨在阐明成牙本质细胞在牙髓先天反应中的作用的研究都集中在革兰氏阳性细菌上,因为这些细菌在初始和中度牙本质龋齿病变中主要是龋菌群。体外实验发现成牙细胞对革兰氏阳性细菌来源的成分敏感,主要是通过细胞膜TLR2识别的脂磷胆酸。我们的研究表明,LTA参与成牙细胞TLR2可触发TLR2和NOD2上调,NF-B核易位,产生各种趋化因子,包括CCL2、CXCL1、CXCL2、CXCL8和CXCL10,同时促进未成熟树突状细胞募集。相反,LTA下调主要牙本质基质成分,包括I型胶原和牙本质唾液磷酸蛋白,以及已知的牙本质形成诱导剂TGF-b1。我们在此提供了额外的数据,显示了NOD2在健康牙髓中的精细定位,以及LTA和合成的TLR2激动剂Pam2CSK4和Pam3CSK4对TLR2、TLR4、NOD2、CCL2和CXCL8基因的差异调节。从上述数据看来,成牙细胞触发的免疫事件构成了中断信号级联的潜在目标,导致过度的免疫反应和牙髓组织坏死受到致龋细菌的攻击。特别是,通过模式识别受体阻止革兰氏阳性细菌识别或信号转导可能是实现这一目标的有价值的策略。该领域的未来研究将为设计新型治疗剂铺平道路,这些治疗剂可以调节成牙髓细胞的行为,促进牙髓的愈合和修复。
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引用次数: 0
P44-expression pattern of APIN and amelotin during formation and regeneration of the junctional epithelium. p44在结膜上皮形成和再生过程中APIN和amelotin的表达谱。
C Nishio, R Wazen, S Kuroda, P Moffatt, A Nanci
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引用次数: 0
P32-distribution and structure of the initial dental enamel formed in incisors of young wild-type and Tabby mice. p32 -野生型和虎斑幼鼠门牙初始牙釉质的分布和结构。
A Sehic, R Peterkova, H Lesot, S Risnes
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引用次数: 0
P9-reduced expression of tight junction proteins ZO-1 and Claudin-1 in ameloblasts and odontoblasts of Epiprofin/Sp6 deficient mice. p9降低epepprofin /Sp6缺陷小鼠成釉细胞和成牙细胞紧密连接蛋白ZO-1和Claudin-1的表达。
L Jiménez, M Aurrekoetxea, G Ibarretxe, P Garcia, S de-Vega, F J Unda
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引用次数: 0
P33-fine structural and immunohistochemical observations of the collar enamel in Lepisosteus and Polypterus, actinopterygian fish. p33 -放光鳍鱼Lepisosteus和polyterus颈釉质精细结构和免疫组化观察。
I Sasagawa, M Ishiyama, H Yokosuka, M Mikami, T Uchida
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引用次数: 0
P8-alteration of tooth development in two-phase organotypic cultures by transient glycogen synthase kinase-3 (GSK-3) inhibition. p8 -瞬时糖原合成酶激酶-3 (GSK-3)抑制对两期器官型培养牙齿发育的影响。
M Aurrekoetxea, G Ibarretxe, P García-Gallastegui, F Unda
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引用次数: 0
P43-implantation of odontoblast progenitors in the rat molar pulp leads to the formation of reparative osteodentin. p43在大鼠磨牙髓内植入成牙细胞祖细胞可形成修复性骨牙素。
Y Harichane, S Dimitrova-Nakov, A Poliard, M Goldberg, O Kellermann
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引用次数: 0
P50-53 prenatal formation of the maxillary and mandibular alveolar bone in humans. 人类上颌和下颌牙槽骨的产前形成。
R J Radlansky, H Renz, U Kalinke, N Tsengelsaikhan, M Konietzny, F Schuster, S Ditscher, C Zimmermann
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引用次数: 0
O40-responses of BrdU-label-retaining dental pulp cells to allogenic tooth transplantation into mouse maxilla. 保留brdu标签的牙髓细胞对同种异体牙移植小鼠上颌的反应。
N Mutoh, M Nakatomi, H Ida-Yonemochi, E Nakagawa, N Tani-Ishii, H Ohshima
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引用次数: 0
O24-induction of human keratinocytes into enamel -secreting ameloblasts. 诱导人角质形成细胞成为分泌珐琅的成釉细胞。
B Wang, L Li, S Du, C Liu, X Hu, Y Chen, Y Zhang
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引用次数: 0
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Bulletin du Groupement international pour la recherche scientifique en stomatologie & odontologie
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