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      Exogenous nitric oxide stimulates the odontogenic differentiation of rat dental pulp stem cells

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          Abstract

          Nitric oxide (NO) is thought to play a pivotal regulatory role in dental pulp tissues under both physiological and pathological conditions. However, little is known about the NO functions in dental pulp stem cells (DPSCs). We examined the direct actions of a spontaneous NO gas-releasing donor, NOC-18, on the odontogenic capacity of rat DPSCs (rDPSCs). In the presence of NOC-18, rDPSCs were transformed into odontoblast-like cells with long cytoplasmic processes and a polarized nucleus. NOC-18 treatment increased alkaline phosphatase activity and enhanced dentin-like mineralized tissue formation and the expression levels of several odontoblast-specific genes, such as runt related factor 2, dentin matrix protein 1 and dentin sialophosphoprotein, in rDPSCs. In contrast, carboxy-PTIO, a NO scavenger, completely suppressed the odontogenic capacity of rDPSCs. This NO-promoted odontogenic differentiation was activated by tumor necrosis factor-NF-κB axis in rDPSCs. Further in vivo study demonstrated that NOC-18-application in a tooth cavity accelerated tertiary dentin formation, which was associated with early nitrotyrosine expression in the dental pulp tissues beneath the cavity. Taken together, the present findings indicate that exogenous NO directly induces the odontogenic capacity of rDPSCs, suggesting that NO donors might offer a novel host DPSC-targeting alternative to current pulp capping agents in endodontics.

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          Stem cell properties of human dental pulp stem cells.

          In this study, we characterized the self-renewal capability, multi-lineage differentiation capacity, and clonogenic efficiency of human dental pulp stem cells (DPSCs). DPSCs were capable of forming ectopic dentin and associated pulp tissue in vivo. Stromal-like cells were reestablished in culture from primary DPSC transplants and re-transplanted into immunocompromised mice to generate a dentin-pulp-like tissue, demonstrating their self-renewal capability. DPSCs were also found to be capable of differentiating into adipocytes and neural-like cells. The odontogenic potential of 12 individual single-colony-derived DPSC strains was determined. Two-thirds of the single-colony-derived DPSC strains generated abundant ectopic dentin in vivo, while only a limited amount of dentin was detected in the remaining one-third. These results indicate that single-colony-derived DPSC strains differ from each other with respect to their rate of odontogenesis. Taken together, these results demonstrate that DPSCs possess stem-cell-like qualities, including self-renewal capability and multi-lineage differentiation.
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            Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens

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              Stem/progenitor cell-mediated de novo regeneration of dental pulp with newly deposited continuous layer of dentin in an in vivo model.

              The ultimate goal of this study is to regenerate lost dental pulp and dentin via stem/progenitor cell-based approaches and tissue engineering technologies. In this study, we tested the possibility of regenerating vascularized human dental pulp in emptied root canal space and producing new dentin on existing dentinal walls using a stem/progenitor cell-mediated approach with a human root fragment and an immunocompromised mouse model. Stem/progenitor cells from apical papilla and dental pulp stem cells were isolated, characterized, seeded onto synthetic scaffolds consisting of poly-D,L-lactide/glycolide, inserted into the tooth fragments, and transplanted into mice. Our results showed that the root canal space was filled entirely by a pulp-like tissue with well-established vascularity. In addition, a continuous layer of dentin-like tissue was deposited onto the canal dentinal wall. This dentin-like structure appeared to be produced by a layer of newly formed odontoblast-like cells expressing dentin sialophosphoprotein, bone sialoprotein, alkaline phosphatase, and CD105. The cells in regenerated pulp-like tissue reacted positively to anti-human mitochondria antibodies, indicating their human origin. This study provides the first evidence showing that pulp-like tissue can be regenerated de novo in emptied root canal space by stem cells from apical papilla and dental pulp stem cells that give rise to odontoblast-like cells producing dentin-like tissue on existing dentinal walls.
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                Author and article information

                Contributors
                yamazata@dent.kyushu-u.ac.jp
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                21 February 2018
                21 February 2018
                2018
                : 8
                : 3419
                Affiliations
                [1 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Department of Molecular Cell Biology and Oral Anatomy, Division of Oral Sciences, , Kyushu University Graduate School of Dental Science, ; Fukuoka, Japan
                [2 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Section of Periodontology, Division of Oral Rehabilitation, Faculty of Dental Science, , Kyushu University, ; Fukuoka, Japan
                [3 ]ISNI 0000 0004 0614 710X, GRID grid.54432.34, Research Fellow of Japan Society for the Promotion of Science, ; Tokyo, Japan
                [4 ]ISNI 0000 0000 9255 8984, GRID grid.89957.3a, Key Laboratory of Oral Diseases of Jiangsu Province and Stomatological School of Nanjing Medical University, ; Nanjing, Jiangsu China
                [5 ]ISNI 0000 0000 9255 8984, GRID grid.89957.3a, Department of Pediatric and Preventive Dentistry, , The Affiliated Stomatological Hospital of Nanjing Medical University, ; Nanjing, Jiangsu China
                [6 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Section of Implant and Rehabilitative Dentistry, Division of Oral Rehabilitation, , Faculty of Dental Science, Kyushu University, ; Fukuoka, Japan
                [7 ]ISNI 0000 0001 1172 4459, GRID grid.412339.e, Department of Oral and Maxillofacial Surgery, , Faculty of Medicine, Saga University, ; Saga, Japan
                [8 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Department of Pediatric Dentistry, Division of Oral Health, Growth & Development, , Kyushu University Graduate School of Dental Science, ; Fukuoka, Japan
                [9 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Kyushu University School of Dentistry, ; Fukuoka, Japan
                Author information
                http://orcid.org/0000-0003-1138-3943
                Article
                21183
                10.1038/s41598-018-21183-6
                5821879
                29467418
                8cf96229-f450-43dd-bdf2-e1023def360c
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 7 December 2017
                : 31 January 2018
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