Identifying potential immuno-oncology targets in salivary gland mucoepidermoid carcinoma based on inflammatory status and treatment response.

BACKGROUND: Mucoepidermoid carcinoma is a rare salivary gland malignant tumour. This study aimed to investigate inflammatory and immune signatures of mucoepidermoid carcinoma by identifying potential proteo-transcriptomic biomarkers towards the development of precision immuno-oncology treatment strategies. METHODS: A total of 30 biopsies obtained from patients diagnosed with mucoepidermoid carcinoma between 2013 and 2022 were analysed after H&E staining for scoring of histological inflammatory stroma subtypes and inflammatory hotspots with QuPath. Multiplex immunofluorescence staining and NanoString nCounter PanCancer IO 360™ panel were used to assess stroma and tumour inflammation signatures in high grade mucoepidermoid carcinoma cases in the tumour microenvironment via proteomics and transcriptomics, respectively. RESULTS: Inflammatory cells within the histological inflammatory stroma inflammatory (HIS-INF/hot) tumour neighbourhoods were greater compared to the histological inflammatory stroma-immune desert (HIS-ID/cold) (p = 0.001). A similar trend was observed between treatment non-responders and responders in stroma neighbourhoods (p = 0.0625) and in stroma-to-interface inflammatory hotspots (p = 0.0081), indicating an augmented inflammatory response in hot tumours and non-responders. Furthermore, there were striking differences in the expression of pan-immune leukocyte marker CD45 between responders and non responders particularly in the tumour neighbourhoods (p = 0.0341), but such were not robust for PD-1 and macrophage fractions. Additionally, transcriptomic analysis revealed key differences in leukocyte activation profiles between responders and non-responders. CONCLUSION: This preliminary report unveils the importance of assessing immune leukocyte cellular fractions and pathways for future prognostic biomarker discoveries in mucoepidermoid carcinoma as per the involvement of CD45-driven inflammatory and immune mediators in high grade mucoepidermoid carcinoma in non-responders to treatment. These findings will potentially contribute to the development of novel personalised immunotherapies.

Mesenchymal stromal cell exosomes enhance dental pulp cell functions and promote pulp-dentin regeneration.

Mesenchymal stromal/stem cell (MSC) therapies are currently being explored for dental pulp regeneration. As the therapeutic effects of MSCs in tissue repair are mediated mainly through the release of extracellular vesicles (EVs) including exosomes, we investigated here the cellular processes and molecular mechanisms modulated by MSC exosomes in dental pulp regeneration. Using dental pulp cell (DPC) cultures, we demonstrated that MSC exosomes could increase DPC migration, proliferation, and odontogenic differentiation. The enhancement of these cellular processes was mediated through exosomal CD73-mediated adenosine receptor activation of AKT and ERK signaling. Consistent with these observations, MSC exosomes increased the expression of dentin matrix proteins and promoted the formation of dentin-like tissue and bridge-like structures in a rat pulp defect model. These effects were comparable to that of mineral trioxide aggregate (MTA) treatment. MSC exosomes also yielded recellularized pulp-dentin tissues in the root canal of endodontically-treated human premolars, following subcutaneous implantation in the mouse dorsum. Together, our findings suggest that MSC exosomes could exert a multi-faceted effect on DPC functions including migration, proliferation and odontogenic differentiation to promote dental pulp regeneration. This study provides the basis for development of MSC exosomes as a cell-free MSC therapeutic alternative for pulp-dentin regeneration.

Salivary gland regeneration: from salivary gland stem cells to three-dimensional bioprinting.

Hyposalivation and severe dry mouth syndrome are the most common complications in patients with head and neck cancer (HNC) after receiving radiation therapy. Conventional treatment for hyposalivation relies on the use of sialogogues such as pilocarpine; however, their efficacy is constrained by the limited number of remnant acinar cells after radiation. After radiotherapy, the salivary gland (SG) secretory parenchyma is largely destroyed, and due to the reduced stem cell niche, this gland has poor regenerative potential. To tackle this, researchers must be able to generate highly complex cellularized 3D constructs for clinical transplantation via technologies, including those that involve bioprinting of cells and biomaterials. A potential stem cell source with promising clinical outcomes to reserve dry mouth is adipose mesenchymal stem cells (AdMSC). MSC-like cells like human dental pulp stem cells (hDPSC) have been tested in novel magnetic bioprinting platforms using nanoparticles that can bind cell membranes by electrostatic interaction, as well as their paracrine signals arising from extracellular vesicles. Both magnetized cells and their secretome cues were found to increase epithelial and neuronal growth of in vitro and ex vivo irradiated SG models. Interestingly, these magnetic bioprinting platforms can be applied as a high-throughput drug screening system due to the consistency in structure and functions of their organoids. Recently, exogenous decellularized porcine ECM was added to this magnetic platform to stimulate an ideal environment for cell tethering, proliferation, and/or differentiation. The combination of these SG tissue biofabrication strategies will promptly allow for in vitro organoid formation and establishment of cellular senescent organoids for aging models, but challenges remain in terms of epithelial polarization and lumen formation for unidirectional fluid flow. Current magnetic bioprinting nanotechnologies can provide promising functional and aging features to in vitro craniofacial exocrine gland organoids, which can be utilized for novel drug discovery and/or clinical transplantation.

Two-Photon Fluorescence Microscopy and Applications in Angiogenesis and Related Molecular Events.

The role of angiogenesis in health and disease have gained considerable momentum in recent years. Visualizing angiogenic patterns and associated events of surrounding vascular beds in response to therapeutic and laboratory-grade biomolecules has become a commonplace in regenerative medicine and the biosciences. To achieve high-quality imaging for elucidating the molecular mechanisms of angiogenesis, the two-photon excitation fluorescence (2PEF) microscopy, or multiphoton fluorescence microscopy is increasingly utilized in scientific investigations. The 2PEF microscope confers several distinct imaging advantages over other fluorescence excitation microscopy techniques-for the observation of in-depth, three-dimensional vascularity in a variety of tissue formats, including fixed tissue specimens and in vivo vasculature in live specimens. Understanding morphological and subcellular changes that occur in cells and tissues during angiogenesis will provide insights to behavioral responses in diseased states, advance the engineering of physiologically relevant tissue models, and provide biochemical clues for the design of therapeutic strategies. We review the applicability and limitations of the 2PEF microscope on the biophysical and molecular-level signatures of angiogenesis in various tissue models. Imaging techniques and strategies for best practices in 2PEF microscopy will be reviewed. Impact Statement Deep live tissue imaging provides unique opportunities to study angiogenesis and associated events in real-time. In contrast to cross-sectional data provided by conventional methods, two-photon microscopy enables high-resolution tissue imaging, data acquisition over time, real-time visualization of angiogenic events, and reduces the number of animal models used in scientific research. This review provides insights on different two-photon microscopy methods and its application in live and deep tissue imaging of angiogenesis on in vitro and in vivo tissues. We believe that the current trends in imaging can transform the investigation of angiogenesis, cancer research, and biofabrication of vascularized tissues.

Graphene nanocoating provides superb long-lasting corrosion protection to titanium alloy.

OBJECTIVE: The presence of metallic species around failed implants raises concerns about the stability of titanium alloy (Ti-6Al-4V). Graphene nanocoating on titanium alloy (GN) has promising anti-corrosion properties, but its long-term protective potential and structural stability remains unknown. The objective was to determine GN's anti-corrosion potential and stability over time. METHODS: GN and uncoated titanium alloy (Control) were challenged with a highly acidic fluorinated corrosive medium (pH 2.0) for up to 240 days. The samples were periodically tested using potentiodynamic polarization curves, electrochemical impedance spectroscopy and inductively coupled plasma-atomic emission spectroscopy (elemental release). The integrity of samples was determined using Raman spectroscopy, X-ray photoelectron spectroscopy, atomic force microscopy and scanning electron microscopy. Statistical analyses were performed with one-sample t-test, paired t-test and one-way ANOVA with Tukey post-hoc test with a pre-set significance level of 5%. RESULTS: There was negligible corrosion and elemental loss on GN. After 240 days of corrosion challenge, the corrosion rate and roughness increased by two and twelve times for the Control whereas remained unchanged for GN. The nanocoating presented remarkably high structural integrity and coverage area (>98%) at all time points tested. SIGNIFICANCE: Graphene nanocoating protects titanium alloy from corrosion and dissolution over a long period while maintaining high structural integrity. This coating has promising potential for persistent protection of titanium and potentially other metallic alloys against corrosion.

New Surgical Model for Bone-Muscle Injury Reveals Age and Gender-Related Healing Patterns in the 5 Lipoxygenase (5LO) Knockout Mouse.

Signaling lipid mediators released from 5 lipoxygenase (5LO) pathways influence both bone and muscle cells, interfering in their proliferation and differentiation capacities. A major limitation to studying inflammatory signaling pathways in bone and muscle healing is the inadequacy of available animal models. We developed a surgical injury model in the vastus lateralis (VL) muscle and femur in 129/SvEv littermates mice to study simultaneous musculoskeletal (MSK) healing in male and female, young (3 months) and aged (18 months) WT mice compared to mice lacking 5LO (5LOKO). MSK defects were surgically created using a 1-mm punch device in the VA muscle followed by a 0.5-mm round defect in the femur. After days 7 and 14 post-surgery, the specimens were removed for microtomography (microCT), histopathology, and immunohistochemistry analyses. In addition, non-injured control skeletal muscles along with femur and L5 vertebrae were analyzed. Bones were microCT phenotyped, revealing that aged female WT mice presented reduced BV/TV and trabecular parameters compared to aged males and aged female 5LOKO mice. Skeletal muscles underwent a customized targeted lipidomics investigation for profiling and quantification of lipid signaling mediators (LMs), evidencing age, and gender related-differences in aged female 5LOKO mice compared to matched WT. Histological analysis revealed a suitable bone-healing process with osteoid deposition at day 7 post-surgery, followed by woven bone at day 14 post-surgery, observed in all young mice. Aged WT females displayed increased inflammatory response at day 7 post-surgery, delayed bone matrix maturation, and increased TRAP immunolabeling at day 14 post-surgery compared to 5LOKO females. Skeletal muscles of aged animals showed higher levels of inflammation in comparison to young controls at day 14 post-surgery; however, inflammatory process was attenuated in aged 5LOKO mice compared to aged WT. In conclusion, this new model shows that MSK healing is influenced by age, gender, and the 5LO pathway, which might serve as a potential target to investigate therapeutic interventions and age-related MSK diseases. Our new model is suitable for bone-muscle crosstalk studies.

Biomechanics of alloplastic mandible reconstruction using biomaterials: The effect of implant design on stress concentration influences choice of material.

INTRODUCTION: Mandibular endoprostheses have been explored extensively as potential methods of alloplastic reconstruction. Studies, however, have demonstrated that for segmental mandibular defects, there are challenges associated with loosening. Another method recently introduced in clinical settings is popular as a design for patient-specific implants for segmental mandibular defect and involves a tray (filled with bone) over the defect with wings on both sides secured with screws. Our aim was to investigate which design better withstands the forces of function since studies have presented favourable results with regard to the wing design. MATERIALS AND METHODS: Two designs, an endoprosthesis with stems and wings were modelled. Finite element analysis was performed, and geometric data obtained from a human-sized mandible. A continuity defect of 20 mm was created digitally at the right mandibular molar region and the modelled segments combined with the endoprosthesis. Boundary conditions were set, and 300-N vertical loads applied in the incisor region. The stress concentrations and displacements were evaluated for the titanium alloy (Group 1-Stem) (Group 2-Wing) and the polycaprolactone (PCL) (Group 3 with stem, Group 4 wing design). RESULTS: For the titanium stem (Group 1), the stress values were in the 557-803 MPa range. The titanium wing (Group 2) design showed markedly reduced stress values in the 20-68 MPa range. The stresses observed for the PCL(Group 3) were in the 66-110 MPa range, and the stress concentration in the PCL wing (Group 4) was observed in the wing and body regions of the scaffolds in the 8-42 MPa range. CONCLUSION: The wing design decreased the areas of stress concentrations significantly compared to an endoprosthesis. PCL alone did not have adequate strength to withstand forces applied even in a design that reduced stress concentrations significantly.

Effect of a calcium hydroxide-based intracanal medicament containing N-2-methyl pyrrolidone as a vehicle against Enterococcus faecalis biofilm

Abstract This study investigated the effect of a calcium hydroxide (CH) paste (CleaniCal®) containing N-2-methyl pyrrolidone (NMP) as a vehicle on Enterococcus faecalis (E. faecalis) biofilms compared with other products containing saline (Calasept Plus™) or propylene glycol (PG) (Calcipex II®). Methodology Standardized bovine root canal specimens were used. The antibacterial effects were measured by colony-forming unit counting. The thickness of bacterial microcolonies and exopolysaccharides was assessed using confocal laser scanning microscopy. Morphological features of the biofilms were observed using field-emission scanning electron microscopy (FE-SEM). Bovine tooth blocks covered with nail polish were immersed into the vehicles and dispelling was observed. The data were analyzed using one-way analysis of variance and Tukey tests (p<0.05). Results CleaniCal® showed the highest antibacterial activity, followed by Calcipex II® (p<0.05). Moreover, NMP showed a higher antibacterial effect compared with PG (p<0.05). The thickness of bacteria and EPS in the CleaniCal® group was significantly lower than that of other materials tested (p<0.05). FE-SEM images showed the specimens treated with Calasept Plus™ were covered with biofilms, whereas the specimens treated with other medicaments were not. Notably, the specimen treated with CleaniCal® was cleaner than the one treated with Calcipex II®. Furthermore, the nail polish on the bovine tooth block immersed in NMP was completely dispelled. Conclusions CleaniCal® performed better than Calasept Plus™ and Calcipex II® in the removal efficacy of E. faecalis biofilms. The results suggest the effect might be due to the potent dissolving effect of NMP on organic substances.

Antibiotics Used in Regenerative Endodontics Modify Immune Response of Macrophages to Bacterial Infection.

INTRODUCTION: Ciprofloxacin, amoxicillin, and metronidazole are antibiotics used in regenerative endodontic therapy (RET). Although their antimicrobial properties are well-documented, there is a lack of information on the effects of these antibiotics on the immune response by host macrophages and periapical healing. Thus, this study had 2 objectives: (1) to determine the immune response of macrophages to bacterial infection in response to the combination of ciprofloxacin or amoxicillin and metronidazole and (2) using conditioned media produced by these macrophages to simulate the periapical microenvironment, to determine the impact on the expression of extracellular matrix (ECM) components by periodontal fibroblasts. METHODS: Macrophages were treated with ciprofloxacin and metronidazole or amoxicillin and metronidazole at 10-1000 µg/mL. The treated macrophages were exposed to lipopolysaccharide, and the pro- and anti-inflammatory cytokines produced were quantified with enzyme-linked immunosorbent assay. Periodontal fibroblasts were treated with conditioned media from these treated macrophages, and the expression of ECM genes was determined by quantitative polymerase chain reaction. RESULTS: Lipopolysaccharides elicited the production of proinflammatory cytokines interleukin 1 beta and tumor necrosis factor alpha by macrophages, but this was suppressed by ciprofloxacin and metronidazole. Moreover, only conditioned media from macrophages treated with ciprofloxacin and metronidazole rescued microbial-induced down-regulation of ECM genes by periodontal fibroblasts. Specifically, ciprofloxacin was the antibiotic responsible for these observations. In contrast, these effects were not observed with amoxicillin and metronidazole. CONCLUSIONS: Apart from disinfection of the root canal system, the combination of ciprofloxacin and metronidazole also exerts an immunomodulatory effect, which may aid in periapical healing.

Graphene-Induced Osteogenic Differentiation Is Mediated by the Integrin/FAK Axis.

Graphene is capable of promoting osteogenesis without chemical induction. Nevertheless, the underlying mechanism(s) remain largely unknown. The objectives here were: (i) to assess whether graphene scaffolds are capable of supporting osteogenesis in vivo and; (ii) to ascertain the participation of the integrin/FAK mechanotransduction axis during the osteogenic differentiation induced by graphene. MSC-impregnated graphene scaffolds (n = 6) were implanted into immunocompromised mice (28 days). Alternatively, MSCs were seeded onto PDMS substrates (modulus of elasticity = 130, 830 and 1300 kPa) coated with a single monomolecular layer of graphene and cultured in basal medium (10 days). The ensuing expressions of FAK-p397, integrin, ROCK1, F-actin, Smad p1/5, RUNX2, OCN and OPN were evaluated by Western blot (n = 3). As controls, MSCs were plated onto uncoated PDMS in the presence of mechanotransduction inhibitors (echistatin, Y27632 and DMH1). MSC-impregnated graphene scaffolds exhibited positive immunoexpression of bone-related markers (RUNX2 and OPN) without the assistance of osteogenic inducers. In vitro, regardless of the stiffness of the underlying PDMS substrate, MSCs seeded onto graphene-coated PDMS substrates demonstrated higher expressions of all tested osteogenic and integrin/FAK proteins tested compared to MSCs seeded onto PDMS alone. Hence, graphene promotes osteogenesis via the activation of the mechanosensitive integrin/FAK axis.

Role of extracellular DNA in Enterococcus faecalis biofilm formation and its susceptibility to sodium hypochlorite

Abstract Objective This study investigated the role of extracellular deoxyribonucleic acid (eDNA) on Enterococcus faecalis ( E. faecalis ) biofilm and the susceptibility of E. faecalis to sodium hypochlorite (NaOCl). Methodology E. faecalis biofilm was formed in bovine tooth specimens and the biofilm was cultured with or without deoxyribonuclease (DNase), an inhibitor of eDNA. Then, the role of eDNA in E. faecalis growth and biofilm formation was investigated using colony forming unit (CFUs) counting, eDNA level assay, crystal violet staining, confocal laser scanning microscopy, and scanning electron microscopy. The susceptibility of E. faecalis biofilm to low (0.5%) or high (5%) NaOCl concentrations was also analyzed by CFU counting. Results CFUs and biofilm formation decreased significantly with DNase treatment (p<0.05). The microstructure of DNase-treated biofilms exhibited less structured features when compared to the control. The volume of exopolysaccharides in the DNase-treated biofilm was significantly lower than that of control (p<0.05). Moreover, the CFUs, eDNA level, biofilm formation, and exopolysaccharides volume were lower when the biofilm was treated with DNase de novo when compared to when DNase was applied to matured biofilm (p<0.05). E. faecalis in the biofilm was more susceptible to NaOCl when it was cultured with DNase (p<0.05). Furthermore, 0.5% NaOCl combined with DNase treatment was as efficient as 5% NaOCl alone regarding susceptibility (p>0.05). Conclusions Inhibition of eDNA leads to decrease of E. faecalis biofilm formation and increase of susceptibility of E. faecalis to NaOCl even at low concentrations. Therefore, our results suggest that inhibition of eDNA would be beneficial in facilitating the efficacy of NaOCl and reducing its concentration.

Influência da condição sistêmica e de hábitos no perfil periodontal: Estudo retrospectivo / The influence of systemic condition and habits in periodontal profile: a retrospective study

Objetivo: avaliar a influência do perfil sistêmico e de hábitos parafuncionais, apertamento e bruxismo no perfil periodontal da população atendida nas clínicas de Periodontia da Universidade do Sagrado Coração (USC). Material e métodos: a coleta de dados foi realizada na Universidade do Sagrado Coração, no período de agosto de 2015 a junho de 2016. Foram avaliados 230 prontuários, dos quais 88 foram incluídos na pesquisa segundo os critérios de inclusão e de exclusão adotados, chegando-se à inclusão de 38,2% dos prontuários. Resultados: as análises mostraram que pacientes diabéticos (n=11) apresentam significativamente mais sítios com profundidades de sondagem (PS) ≥ 8 mm do que pacientes não diabéticos (n=77 | p=0,01); pacientes não hipertensos (n=65) tiveram significativamente mais sítios com recessões gengivais (RG) entre 4 mm e 5 mm do que pacientes hipertensos (n=24 | p=0,049); e pacientes sem hábitos parafuncionais de apertar ou ranger os dentes (n=75) tiveram significativamente mais sítios com perda de nível de inserção clínica (NIC) entre 6 mm e 7 mm do que pacientes sem hábitos parafuncionais de apertar ou ranger os dentes (n=13 | p=0,023). Conclusão: dentro dos limites do presente estudo, pôde-se concluir que o diabetes foi confirmado como fator de risco para doenças periodontais, constatando-se maior a quantidade de sítios com grandes PS e que hábitos parafuncionais de apertamento ou bruxismo não contribuem para o aumento do NIC.

Objective: to evaluate the influence of systemic profile and parafunctional habits, clenching and bruxism on periodontal profile of the population treated in Periodontics clinics at Universidade do Sagrado Coração (USC). Material and methods: data collection was performed at the USC, in the period from August 2015 to June 2016. We evaluated 230 records in which 88 were included in the study according to the inclusion criteria and exclusion criteria, coming to the inclusion 38.2% of the records. Results: diabetic patients (n=11) showed significantly more sites with probing depths (PD) ≥ 8 mm than non-diabetic patients (n=77 | p=0.01), non-hypertensive (n=65) had significantly more sites with gingival recession (GR) between 4-5 mm than hypertensive patients (n=24) | p=0.049) and patients without parafunctional habits of clenching or grinding teeth (n=75) had significantly more sites with loss of clinical attachment level (CAL) between 6-7 mm than patients without parafunctional habits of clenching and bruxism (n=13 | p=0.023). Conclusion: within the limits of this study, it can be concluded that diabetes was confirmed as a risk factor for periodontal disease, with a greater quantity of sites with deeper PD and parafunctional habits of clenching or bruxism did not contribute to increase CAL.

Reliability, failure probability, and strength of resin-based materials for CAD/CAM restorations

ABSTRACT Objective: This study investigated the Weibull parameters and 5% fracture probability of direct, indirect composites, and CAD/CAM composites. Material and Methods: Discshaped (12 mm diameter x 1 mm thick) specimens were prepared for a direct composite [Z100 (ZO), 3M-ESPE], an indirect laboratory composite [Ceramage (CM), Shofu], and two CAD/CAM composites [Lava Ultimate (LU), 3M ESPE; Vita Enamic (VE), Vita Zahnfabrik] restorations (n=30 for each group). The specimens were polished, stored in distilled water for 24 hours at 37°C. Weibull parameters (m= modulus of Weibull, σ0= characteristic strength) and flexural strength for 5% fracture probability (σ5%) were determined using a piston-on-three-balls device at 1 MPa/s in distilled water. Statistical analysis for biaxial flexural strength analysis were performed either by both one-way ANOVA and Tukey's post hoc (α=0.05) or by Pearson's correlation test. Results: Ranking of m was: VE (19.5), LU (14.5), CM (11.7), and ZO (9.6). Ranking of σ0 (MPa) was: LU (218.1), ZO (210.4), CM (209.0), and VE (126.5). σ5% (MPa) was 177.9 for LU, 163.2 for CM, 154.7 for Z0, and 108.7 for VE. There was no significant difference in the m for ZO, CM, and LU. VE presented the highest m value and significantly higher than ZO. For σ0 and σ5%, ZO, CM, and LU were similar but higher than VE. Conclusion: The strength characteristics of CAD/ CAM composites vary according to their composition and microstructure. VE presented the lowest strength and highest Weibull modulus among the materials.

Bioactivity, physical and chemical properties of MTA mixed with propylene glycol

AbstractObjective To investigate the physical (setting time, hardness, flowability, microstructure) and chemical (pH change, calcium release, crystallinity) properties and the biological outcomes (cell survival and differentiation) of mineral trioxide aggregate (MTA) mixed using different proportions of propylene glycol (PG) and water.Material and Methods White MTA was mixed with different water/PG ratios (100/0, 80/20 and 50/50). Composition (XRD), microstructure (SEM), setting time (ASTM C266-13), flowability (ANSI/ADA 57-2000), Knoop hardness (100 g/10 s) and chemical characteristics (pH change and Ca2+ release for 7 days) were evaluated. Cell proliferation, osteo/odontoblastic gene expression and mineralization induced by MTA mixed with PG were evaluated. MTA discs (5 mm in diameter, 2 mm thick) were prepared and soaked in culture medium for 7 days. Next, the discs were removed and the medium used to culture dental pulp stem cells (DPSC) for 28 days. Cells survival was evaluated using MTS assay (24, 72 and 120 h) and differentiation with RT-PCR (ALP, OCN, Runx2, DSPP and MEPE) and alizarin red staining (7 and 14 days). Data were analysed using one-way ANOVA and Tukey’s post-hoc analysis (a=0.05).Results The addition of PG significantly increased setting time, flowability and Ca2+ release, but it compromised the hardness of the material. SEM showed that 50/50 group resulted porous material after setting due to the incomplete setting reaction, as shown by XRD analysis. The addition of PG (80/20 and 50/50) was not capable to improve cell proliferation or to enhance gene expression, and mineralized deposition of DPSC after 7 and 14 days as compared to the 100/0.Conclusion Except for flowability, the addition of PG did not promote further improvements on the chemical and physical properties evaluated, and it was not capable of enhancing the bioactivity of the MTA.

Inducing pluripotency for disease modeling, drug development and craniofacial applications.

INTRODUCTION: The induced pluripotent stem cells (iPSCs) have characteristics similar to embryonic stem cells, including the capability of self-renewal and large-scale expansion and the ability to differentiate into all types of cells including germ cells, which defines pluripotency. Using iPSC avoids problems of immunological rejection and ethical controversy. The possible future uses of iPSC are diverse and go beyond the differentiation into somatic cells for regeneration of damaged tissues. AREAS COVERED: A unique feature of iPSC is the potential to generate patient disease-specific tissues. Thus, cells from patients can be differentiated into relevant cells of interest for drug screening, characterization of drug effects and cytotoxic assays. This review presents key aspects related to iPSC, such as their generation, potential for disease modeling, treatment, drug development and future contributions to the craniofacial complex. EXPERT OPINION: It is undisputable that the evolution in iPSC knowledge will improve the approaches for drug screening and development, help to understand and treat disease origins and mechanisms and provide new strategies to clinical treatment. However, it is necessary to fine-tune protocols to establish iPSCs that are cost-effective and safe for clinical use.

Use of assisted reproductive technology to separate sperm from human immunodeficiency virus infected men resulting in pregnancy among serodiscordant couples

Due to HIV care improvement, discordant couples more frequently seek help in order to conceive their own biological child. Besides the advance of antiretroviral therapy, unprotected intercourse is not a complete safe option, carrying a low but still present risk of HIV transmission. We report 10 serodiscordant couples in whom the male partner is HIV positive, submitted to sperm washing and intrauterine insemination. The procedure resulted in four pregnancies and no HIV transmission to mother or child was observed. Techniques of assisted reproduction can help HIV discordant couples to conceive biological offspring and is a safer option than unprotected intercourse.

Engenharia de tecidos com células-tronco de dentes decíduos e scaffolds injetáveis e a formação de polpa dental funcional / Stem cells from exfoliated deciduous teeth and self-assembling nanofiber and recombinant human collagen I scaffolds allows for the engineering of a functional dental pulp

A translação da regeneração pulpar com células tronco para a clinica requerirá o uso de scaffolds injetáveis. O objetivo foi estudar o comportamento de células tronco obtidas de dentes decíduos exfoliados (SHED) injetados em canais radiculares de pré-molares humanos com ápice aberto com scaffold de colágeno recombinante humano tipo I (rhC-I) e a base de nanofibras auto-organizáveis (SA). Para determinar a viabilidade e potencial de diferenciação de SHED in vitro, raízes nao instrumentadas foram posicionadas com o ápice em meio de cultura. SHED ressuspendida em rhC e SA foram injetadas nos canais (n=24, 5X105 células/mL). Os controles foram SHED e scaffolds sozinhos. Marcadores para diferenciação odontoblastica (DSPP, DMP-1 e MEPE) foram avaliados semanalmente por RT-PCR por 28 dias. Para avaliar a diferenciação odontoblástica e formação de tecido in vivo, SHED transuzida com GFP foram injetadas em canais radiculares (n=8, 106 célulass/mL) utilizando os mesmos grupos e implantadas subcutaneamente em camundongos imunodeprimidos. O controle (C+) foi um pré-molar humano extraído. Analise estatística foi feita com ANOVA (=0.05). Os marcadores de diferenciação odontoblástica aumentaram para SA e rhC-I mas nao nos controles. Crescimento de tecido pulpar-símile ( do que 60% do comprimento da raiz) foi observado em 75% dos implantes para SA e rhC-I e 0% nos controles. Analise de imunohistoquimica para GFP confirmou a origem tecidual a partir de SHED. PCNA e ensaio de TUNEL mostraram alta ativiade proliferativa e poucas células apoptóticas. Injeções de tetraciclina evidenciaram neoformação de dentina. A densidade microvascular e nomero de odontoblastos delineando a dentinta foi similar em rhC-I, SA e C+. A associação de SHED com scaffolds injetáveis foi capaz de originar um tecido pulpar capaz de produzir dentina e constitui um passo a mais frente ao objetivo de regeneração pulpar em pacientes humanos

The translation of dental pulp regeneration with stem cells to the clinic will require the use of injectable scaffolds. The aim was to study the behavior of stem cells from exfoliated deciduous teeth (SHED) injected in the root canal of opened-apex human premolars with either recombinant human collagen I (rhC-I) or selfassembling nanofiber (SA) scaffolds. To assess in vitro SHED viability and differentiative potential, non-instrumented roots were set with the apex in culture media. SHED were mixed in rhC-I or SA and injected into canals (n=24, 5X105 cells/mL). Controls were SHED or scaffolds alone. Odontoblastic differentiation markers (DSPP, DMP-1 and MEPE) were assessed weekly by RT-PCR for 28 days. To evaluate odontoblast differentiation and tissue formation in vivo, SHED transduced with GFP were injected in canals (n=8, 106 cells/mL) using same groups and implanted subcutaneously in immunodeficient mice. Positive control (C+) was extracted premolar. Statistic was done with ANOVA (=0.05). Odontoblastic differentiation markers increased in SA and rhC-I but not in controls. Pulp-like tissue growth ( than 60% of root length) was observed in 75% of implants for SA and rhC-I and 0% in controls. GFP staining confirmed SHEDs tissue origin. PCNA staining and TUNEL assay showed high proliferative activity and few apoptotic cells. Tetracycline injections showed newly formed dentin. Microvessel density and odontoblastic-like cell number lining dentin were similar in rhC-I, SA and C+. Injectable scaffolds and SHED allowed for the engineering of a pulp-like tissue and constitute one step forward towards the goal of dental p ulp regeneration in human patients

Engenharia de tecidos com células-tronco de dentes decíduos e scaffolds injetáveis e a formação de polpa dental funcional / Stem cells from exfoliated deciduous teeth and self-assembling nanofiber and recombinant human collagen I scaffolds allows for the engineering of a functional dental pulp

A translação da regeneração pulpar com células tronco para a clinica requerirá o uso de scaffolds injetáveis. O objetivo foi estudar o comportamento de células tronco obtidas de dentes decíduos exfoliados (SHED) injetados em canais radiculares de pré-molares humanos com ápice aberto com scaffold de colágeno recombinante humano tipo I (rhC-I) e a base de nanofibras auto-organizáveis (SA). Para determinar a viabilidade e potencial de diferenciação de SHED in vitro, raízes nao instrumentadas foram posicionadas com o ápice em meio de cultura. SHED ressuspendida em rhC e SA foram injetadas nos canais (n=24, 5X105 células/mL). Os controles foram SHED e scaffolds sozinhos. Marcadores para diferenciação odontoblastica (DSPP, DMP-1 e MEPE) foram avaliados semanalmente por RT-PCR por 28 dias. Para avaliar a diferenciação odontoblástica e formação de tecido in vivo, SHED transuzida com GFP foram injetadas em canais radiculares (n=8, 106 célulass/mL) utilizando os mesmos grupos e implantadas subcutaneamente em camundongos imunodeprimidos. O controle (C+) foi um pré-molar humano extraído. Analise estatística foi feita com ANOVA (=0.05). Os marcadores de diferenciação odontoblástica aumentaram para SA e rhC-I mas nao nos controles. Crescimento de tecido pulpar-símile ( do que 60% do comprimento da raiz) foi observado em 75% dos implantes para SA e rhC-I e 0% nos controles. Analise de imunohistoquimica para GFP confirmou a origem tecidual a partir de SHED. PCNA e ensaio de TUNEL mostraram alta ativiade proliferativa e poucas células apoptóticas. Injeções de tetraciclina evidenciaram neoformação de dentina. A densidade microvascular e nomero de odontoblastos delineando a dentinta foi similar em rhC-I, SA e C+. A associação de SHED com scaffolds injetáveis foi capaz de originar um tecido pulpar capaz de produzir dentina e constitui um passo a mais frente ao objetivo de regeneração pulpar em pacientes humanos.

The translation of dental pulp regeneration with stem cells to the clinic will require the use of injectable scaffolds. The aim was to study the behavior of stem cells from exfoliated deciduous teeth (SHED) injected in the root canal of opened-apex human premolars with either recombinant human collagen I (rhC-I) or self assembling nanofiber (SA) scaffolds. To assess in vitro SHED viability and differentiative potential, non-instrumented roots were set with the apex in culture media. SHED were mixed in rhC-I or SA and injected into canals (n=24, 5X105 cells/mL). Controls were SHED or scaffolds alone. Odontoblastic differentiation markers (DSPP, DMP-1 and MEPE) were assessed weekly by RT-PCR for 28 days. To evaluate odontoblast differentiation and tissue formation in vivo, SHED transduced with GFP were injected in canals (n=8, 106 cells/mL) using same groups and implanted subcutaneously in immunodeficient mice. Positive control (C+) was extracted premolar. Statistic was done with ANOVA (=0.05). Odontoblastic differentiation markers increased in SA and rhC-I but not in controls. Pulp-like tissue growth ( than 60% of root length) was observed in 75% of implants for SA and rhC-I and 0% in controls. GFP staining confirmed SHEDs tissue origin. PCNA staining and TUNEL assay showed high proliferative activity and few apoptotic cells. Tetracycline injections showed newly formed dentin. Microvessel density and odontoblastic-like cell number lining dentin were similar in rhC-I, SA and C+. Injectable scaffolds and SHED allowed for the engineering of a pulp-like tissue and constitute one step forward towards the goal of dental p ulp regeneration in human patients.

Effect of acid etching of glass ionomer cement surface on the microleakage of sandwich restorations

The purposes of this study were to evaluate the sealing ability of different glass ionomer cements (GICs) used for sandwich restorations and to assess the effect of acid etching of GIC on microleakage at GIC-resin composite interface. Forty cavities were prepared on the proximal surfaces of 20 permanent human premolars (2 cavities per tooth), assigned to 4 groups (n=10) and restored as follows: Group CIE - conventional GIC (CI) was applied onto the axial and cervical cavity walls, allowed setting for 5 min and acid etched (E) along the cavity margins with 35 percent phosphoric acid for 15 s, washed for 30 s and water was blotted; the adhesive system was applied and light cured for 10 s, completing the restoration with composite resin light cured for 40 s; Group CIN - same as Group CIE, except for acid etching of the CI surface; Group RME - same as CIE, but using a resin modified GIC (RMGIC); Group RMN - same as Group RME, except for acid etching of the RMGIC surface. Specimens were soaked in 1 percent methylene blue dye solution at 24°C for 24 h, rinsed under running water for 1 h, bisected longitudinally and dye penetration was measured following the ISO/TS 11405-2003 standard. Results were statistically analyzed by Kruskal-Wallis and chi-square tests (a=0.05). Dye penetration scores were as follow: CIE - 2.5; CIN - 2.5; RME - 0.9; and RMN - 0.6. The results suggest that phosphoric acid etching of GIC prior to the placement of composite resin does not improve the sealing ability of sandwich restorations. The RMGIC was more effective in preventing dye penetration at the GIC-resin composite-dentin interfaces than CI.

Effect of acid etching of glass ionomer cement surface on the microleakage of sandwich restorations.

The purposes of this study were to evaluate the sealing ability of different glass ionomer cements (GICs) used for sandwich restorations and to assess the effect of acid etching of GIC on microleakage at GIC-resin composite interface. Forty cavities were prepared on the proximal surfaces of 20 permanent human premolars (2 cavities per tooth), assigned to 4 groups (n=10) and restored as follows: Group CIE - conventional GIC (CI) was applied onto the axial and cervical cavity walls, allowed setting for 5 min and acid etched (E) along the cavity margins with 35% phosphoric acid for 15 s, washed for 30 s and water was blotted; the adhesive system was applied and light cured for 10 s, completing the restoration with composite resin light cured for 40 s; Group CIN - same as Group CIE, except for acid etching of the CI surface; Group RME - same as CIE, but using a resin modified GIC (RMGIC); Group RMN - same as Group RME, except for acid etching of the RMGIC surface. Specimens were soaked in 1% methylene blue dye solution at 24 degrees C for 24 h, rinsed under running water for 1 h, bisected longitudinally and dye penetration was measured following the ISO/TS 11405-2003 standard. Results were statistically analyzed by Kruskal-Wallis and chi-square tests (a=0.05). Dye penetration scores were as follow: CIE - 2.5; CIN - 2.5; RME - 0.9; and RMN - 0.6. The results suggest that phosphoric acid etching of GIC prior to the placement of composite resin does not improve the sealing ability of sandwich restorations. The RMGIC was more effective in preventing dye penetration at the GIC-resin composite-dentin interfaces than CI.