| 1. |
- Lira-Junior, Ronaldo, et al.
(författare)
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S100A12 Expression Is Modulated During Monocyte Differentiation and Reflects Periodontitis Severity
- 2020
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Ingår i: Frontiers in Immunology. - : Frontiers Media S.A.. - 1664-3224. ; 11
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Tidskriftsartikel (refereegranskat)abstract
- S100A12 is a calcium-binding protein of the S100 subfamily of myeloid-related proteins that acts as an alarmin to induce a pro-inflammatory innate immune response. It has been linked to several chronic inflammatory diseases, however its role in the common oral immunopathology periodontitis is largely unknown. Previous in vitro monoculture experiments indicate that S100A12 production decreases during monocyte differentiation stages, while the regulation within tissue is poorly defined. This study evaluated S100A12 expression in monocyte subsets, during monocyte-to-macrophage differentiation and following polarization, both in monoculture and in a tissue context, utilizing a three-dimensional co-culture oral tissue model. Further, we explored the involvement of S100A12 in periodontitis by analyzing its expression in peripheral circulation and gingival tissue, as well as in saliva. We found that S100A12 expression was higher in classical than in non-classical monocytes. S100A12 expression and protein secretion declined significantly during monocyte-to-macrophage differentiation, while polarization of monocyte-derived macrophages had no effect on either. Peripheral monocytes from periodontitis patients had higher S100A12 expression than monocytes from controls, a difference particularly observed in the intermediate and non-classical monocyte subsets. Further, monocytes from periodontitis patients displayed an increased secretion of S100A12 compared with monocytes from controls. In oral tissue cultures, monocyte differentiation resulted in increased S100A12 secretion over time, which further increased after inflammatory stimuli. Likewise, S100A12 expression was higher in gingival tissue from periodontitis patients where monocyte-derived cells exhibited higher expression of S100A12 in comparison to non-periodontitis tissue. In line with our findings, patients with severe periodontitis had significantly higher levels of S100A12 in saliva compared to non-periodontitis patients, and the levels correlated to clinical periodontal parameters. Taken together, S100A12 is predominantly secreted by monocytes rather than by monocyte-derived cells. Moreover, S100A12 is increased in inflamed tissue cultures, potentially as a result of enhanced production by monocyte-derived cells. This study implicates the involvement of S100A12 in periodontitis pathogenesis, as evidenced by increased S100A12 expression in inflamed gingival tissue, which may be due to altered circulatory monocytes in periodontitis.
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| 2. |
- Richards, David A, et al.
(författare)
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Integrating quantitative and qualitative data and findings when undertaking randomised controlled trials.
- 2019
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Ingår i: BMJ Open. - : BMJ Publishing Group Ltd. - 2044-6055. ; 9:11
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Tidskriftsartikel (refereegranskat)abstract
- It is common to undertake qualitative research alongside randomised controlled trials (RCTs) when evaluating complex interventions. Researchers tend to analyse these datasets one by one and then consider their findings separately within the discussion section of the final report, rarely integrating quantitative and qualitative data or findings, and missing opportunities to combine data in order to add rigour, enabling thorough and more complete analysis, provide credibility to results, and generate further important insights about the intervention under evaluation. This paper reports on a 2 day expert meeting funded by the United Kingdom Medical Research Council Hubs for Trials Methodology Research with the aims to identify current strengths and weaknesses in the integration of quantitative and qualitative methods in clinical trials, establish the next steps required to provide the trials community with guidance on the integration of mixed methods in RCTs and set-up a network of individuals, groups and organisations willing to collaborate on related methodological activity. We summarise integration techniques and go beyond previous publications by highlighting the potential value of integration using three examples that are specific to RCTs. We suggest that applying mixed methods integration techniques to data or findings from studies involving both RCTs and qualitative research can yield insights that might be useful for understanding variation in outcomes, the mechanism by which interventions have an impact, and identifying ways of tailoring therapy to patient preference and type. Given a general lack of examples and knowledge of these techniques, researchers and funders will need future guidance on how to undertake and appraise them.
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| 3. |
- Rudolph, D., et al.
(författare)
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Experimental and shell-model study of excited states in 55Fe29 and related notes on 55Cu26
- 2021
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Ingår i: Physical Review C. - : American Physical Society. - 2469-9985 .- 2469-9993. ; 104:4
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Tidskriftsartikel (refereegranskat)abstract
- The fusion-evaporation reaction 32S+28Si at 125-MeV beam energy was used to populate excited states in 55Fe. Combining the Gammasphere spectrometer with ancillary devices including the Microball CsI(Tl) array and a shell of neutron detectors, a comprehensive level scheme could be derived. The experimental results are compared with theoretical results from shell-model calculations. Taking into account isospin-symmetry breaking terms is found to considerably improve the shell-model description for 55Fe. This motivated a predictive case study of near-yrast states in the mirror nucleus 55Cu.
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| 4. |
- Rudolph, D., et al.
(författare)
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Single-particle and collective excitations in the N=28 isotones 54Fe and 53Mn
- 2020
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Ingår i: Physical Review C. - : American Physical Society. - 2469-9985. ; 102:1
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Tidskriftsartikel (refereegranskat)abstract
- The fusion-evaporation reaction 32S + 28Si at 125 MeV beam energy was used to populate high-spin states in the semimagic N = 28 nuclei 53Mn and 54Fe. With a combination of the Gammasphere spectrometer and ancillary devices including the Microball CsI(Tl) array, extensive high-spin level schemes are derived. They exhibit rotational-like collective structures and competing single-particle excitations. The experimental results are compared with predictions from shell-model calculations, for which the inclusion of isopin-symmetry-breaking terms is found to improve the description. An interpretation of the high-spin states is put forward using cranked Nilsson-Strutinsky calculations, indicative of contributions from collective excitations beyond some 8-MeV excitation energy and highlighting the importance of the g9/2 intruder orbital in this energy range.
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