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Träfflista för sökning "WFRF:(Konttinen J) "

Search: WFRF:(Konttinen J)

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  • Kouri, V. P., et al. (author)
  • Neutrophils produce interleukin-17B in rheumatoid synovial tissue
  • 2014
  • In: Rheumatology. - : Oxford University Press (OUP). - 1462-0324 .- 1462-0332. ; 53:1, s. 39-47
  • Journal article (peer-reviewed)abstract
    • Objective: T helper 17 (Th17) and mast cells produce IL-17A in RA and critically contribute to the pathogenesis of RA. However, the complete IL-17 cytokine profile in RA is unknown. The aim of the study was to systematically study the expression of IL-17 family cytokines in RA. Methods: The expression of all IL-17 cytokines in RA synovium and pannus as well as in the synovium of OA was determined using quantitative RT-PCR (qRT-PCR). IL-17A and IL-17B were immunostained. Peripheral blood neutrophils were analysed for IL-17B. The effect of IL-17B alone or in combination with TNF-α was tested in vitro on fibroblasts and endothelial cells. Results: In all tissues IL-17B was the most expressed IL-17 family cytokine, found in lining but most strongly expressed in human neutrophil elastase containing polymorphonuclear cells. This pattern was distinct from that of IL-17A, which was found in mast cell tryptase immunoreactive cells. Circulating neutrophils contained IL-17B, verifying the in vivo results. Fibroblasts up-regulated the expression of IL-17RB, a putative receptor of IL-17B, after TNF-α stimulation. IL-17B significantly enhanced TNF-α-induced production of G-CSF and IL-6 in fibroblasts. Conclusion: IL-17B, which is present in synovium, may contribute to the pathogenesis of RA. IL-17B can enhance the effects of TNF-α on the production of cytokines and chemokines that control immune cell trafficking and neutrophil homeostasis in the inflamed tissues. © The Author 2013. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
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  • Mackiewicz, Z, et al. (author)
  • Receptor activator of nuclear factor kappa B ligand in an experimental intervertebral disc degeneration.
  • 2009
  • In: Clinical and experimental rheumatology. - 0392-856X. ; 27:2, s. 299-306
  • Journal article (peer-reviewed)abstract
    • This study was designed to clarify the role of the receptor activator of nuclear factor kappa B ligand (RANKL) in the process of discus degeneration and spondylarthrosis. It was hypothesized that experimental discus lesion would initiate not only local bone remodelling but also increased osteoclast formation on a location remote to the injury site due to altered spinal biomechanics. It was speculated that these changes in vertebral bone remodelling could be reflected in an increased RANKL expression.
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  • van Osch, G. J., et al. (author)
  • Cartilage repair: past and future--lessons for regenerative medicine
  • 2009
  • In: Journal of Cellular and Molecular Medicine. - 1582-4934. ; 13:5, s. 792-810
  • Journal article (peer-reviewed)abstract
    • Since the first cell therapeutic study to repair articular cartilage defects in the knee in 1994, several clinical studies have been reported. An overview of the results of clinical studies did not conclusively show improvement over conventional methods, mainly because few studies reach level I of evidence for effects on middle or long term. However, these explorative trials have provided valuable information about study design, mechanisms of repair and clinical outcome and have revealed that much is still unknown and further improvements are required. Furthermore, cellular and molecular studies using new technologies such as cell tracking, gene arrays and proteomics have provided more insight in the cell biology and mechanisms of joint surface regeneration. Besides articular cartilage, cartilage of other anatomical locations as well as progenitor cells are now considered as alternative cell sources. Growth Factor research has revealed some information on optimal conditions to support cartilage repair. Thus, there is hope for improvement. In order to obtain more robust and reproducible results, more detailed information is needed on many aspects including the fate of the cells, choice of cell type and culture parameters. As for the clinical aspects, it becomes clear that careful selection of patient groups is an important input parameter that should be optimized for each application. In addition, the study outcome parameters should be improved. Although reduced pain and improved function are, from the patient's perspective, the most important outcomes, there is a need for more structure/tissue-related outcome measures. Ideally, criteria and/or markers to identify patients at risk and responders to treatment are the ultimate goal for these more sophisticated regenerative approaches in joint surface repair in particular, and regenerative medicine in general.
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  • Kallio, S., et al. (author)
  • Sensitivity study of fluid dynamic effects on nitric oxide formation in CFB combustion of wood
  • 2002
  • In: Proc. of the 7th International Circulating Fluidized Bed. - 0920804985 ; , s. 757-764
  • Book chapter (other academic/artistic)abstract
    • The paper presents results from simulations by a 1.5D numerical model developed to study the formation of the NO and N2O emissions in a circulating fluidized bed combustor (CFBC) under different operating conditions and burning different fuels. A comprehensive kinetic scheme for the homogeneous chemistry and a single particle model for char combustion are used. Fluiddynamic factors, including gas mixing and release of volatiles, are investigated in the case of wood combustion under normal air staging conditions. The pattern of release of volatiles, the mixing of secondary air, and the lateral mixing of gas are observed to play significant roles in the formation of the relatively high NO emissions from combustion of wood. Comparisons are made with measurement data and also with coal combustion.
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  • Kilpi, F, et al. (author)
  • The Authors Respond
  • 2018
  • In: Epidemiology (Cambridge, Mass.). - 1531-5487. ; 29:4, s. E37-E37
  • Journal article (other academic/artistic)
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  • Kilpinen, P., et al. (author)
  • Towards a quantitative understanding of NOx and N2O emission formation in full-scale circulating fluidised bed combustors
  • 2001
  • In: In Proceedings of the 16th International Conference on Fluidized Bed Combustion--FBC01, held in Reno, Nevada, USA, May 13-16, 2001.
  • Conference paper (peer-reviewed)abstract
    • A mathematical tool is being developed for studying the nitrogen oxide emission formation in circulating fluidised bed combustors. The model is based on detailed homogeneous and heterogeneous chemical kinetics and a simplified, reasonable description of CFB hydrodynamics with presumed temperature distribution (Kilpinen et al, 1999a). With the model different fuels and fuel mixtures can be compared in regard to their nitrogen oxide emission formation tendency at typical CFBC conditions. In this paper the structure of the CFBC model and its submodels are shortly described in present form. The CFBC model is tested for nitrogen oxide prediction at normal air staging conditions in a 12 MW CFB with bituminous coal and wood chips as the fuel, respectively. Comparisons of modelling results with detailed gas concentration profiles measured inside the furnace are made. The relative importance of homogeneous and heterogeneous reactions on NO and N2O concentration profiles is illustrated based on a quantitative reaction rate analysis at different parts in the combustor. The importance of effects of radical removal on particle surfaces, and thus, a decreased CO burnout and, simultaneously, enhanced rates of catalytic bed/char reactions on nitrogen oxides’ destruction are discussed.
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  • Laukkanen, P, et al. (author)
  • Electronic and structural properties of GaAs(100)(2x4) and InAs(100)(2x4) surfaces studied by core-level photoemission and scanning tunneling microscopy
  • 2005
  • In: Physical Review B (Condensed Matter and Materials Physics). - 1098-0121. ; 72:4
  • Journal article (peer-reviewed)abstract
    • Electronic and structural properties of GaAs(100)(2x4), InAs(100)(2x4), and Sb/InAs(100)(2x4) reconstructed surfaces have been studied by synchrotron-radiation photoelectron spectroscopy and scanning tunneling microscopy (STM). Based on the difference spectrum of As 3d core-level spectra of III-As(100)(2x4), measured in different surface-sensitivity conditions, as well as the line shape of the As 3d emission from the Sb-induced (2x4) surface, we give evidence that the As 3d spectra of GaAs(100)(2x4) and InAs(100)(2x4) consist of two surface-core-level-shifted components. One of them is shifted about 0.2 eV to the lower kinetic energy from the bulk component. On the basis of the relative component intensities, this surface-shifted As 3d component is assigned to the emission from the first-layer As dimers in the established model of the (2x4) surface. The other component, shifted about 0.3 eV to the higher kinetic energy, is connected to the third-layer As-dimer site. The comparison of the core-level results between GaAs(100)(2x4) and InAs(100)(2x4) suggests that the alpha 2 phase, which has one As dimer in both the first and third atomic layers per unit cell, exists on GaAs(100)(2x4), similarly to the case of InAs(100)(2x4), as predicted in theory but not observed to date. Furthermore, the STM observation of the GaAs(100)(2x4)alpha 2 phase is reported.
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  • Pöllänen, E., et al. (author)
  • Differential influence of peripheral and systemic sex steroids on skeletal muscle quality in pre- and postmenopausal women
  • 2011
  • In: Aging Cell. - : Wiley. - 1474-9718. ; 10:4, s. 650-660
  • Journal article (peer-reviewed)abstract
    • Aging is associated with gradual decline of skeletal muscle strength and mass often leading to diminished muscle quality. This phenomenon is known as sarcopenia and affects about 30% of the over 60-year-old population. Androgens act as anabolic agents regulating muscle mass and improving muscle performance. The role of female sex steroids as well as the ability of skeletal muscle tissue to locally produce sex steroids has been less extensively studied. We show that despite the extensive systemic deficit of sex steroid hormones in postmenopausal compared to premenopausal women, the hormone content of skeletal muscle does not follow the same trend. In contrast to the systemic levels, muscle tissue of post- and premenopausal women had similar concentrations of dehydroepiandrosterone and androstenedione, while the concentrations of estradiol and testosterone were significantly higher in muscle of the postmenopausal women. The presence of steroidogenetic enzymes in muscle tissue indicates that the elevated postmenopausal steroid levels in skeletal muscle are because of local steroidogenesis. The circulating sex steroids were associated with better muscle quality while the muscle concentrations reflected the amount of infiltrated fat within muscle tissue. We conclude that systemically delivered and peripherally produced sex steroids have distinct roles in the regulation of neuromuscular characteristics during aging.
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  • Vasara, Anna I, et al. (author)
  • Subchondral bone reaction associated with chondral defect and attempted cartilage repair in goats.
  • 2004
  • In: Calcified tissue international. - : Springer Science and Business Media LLC. - 0171-967X .- 1432-0827. ; 74:1, s. 107-14
  • Journal article (peer-reviewed)abstract
    • Repair of cartilage damage with autologous chondrocyte transplantation (ACT) has become popular in clinical use during the past few years. Although clinical results have mostly been successful, several unanswered questions remain regarding the biological mechanism of the repair process. The aim of this study was to develop a goat model for ACT. The repair was not successful due to the graft delamination, but we characterize the subchondral changes seen after the procedure. A chondral lesion was created in 14 goat knees, operated on 1 month later with ACT, and covered with periosteum or a bioabsorbable poly-L/D-lactide scaffold. After 3 months, only two of the five lesions repaired with ACT showed partly hyaline-like repair tissue, and all lesions (n = 4) with the scaffold failed. Even though the lesions did not extend through the calcified cartilage, the bone volume and collagen organization of bone structure were decreased when assessed by quantitative polarized light microscopy. There was a significant loss of bone matrix and distortion of the trabecular structure of subchondral bone, which extended several millimeters into the bone. The subchondral bone demonstrated strong hyaluronan staining in the bone marrow and cartilaginous areas with signs of endochondral ossification, suggesting structural remodeling of the bone. The goat model used here proved not to be an optimal model for ACT. The changes in subchondral bone may alter the biomechanical properties of the subchondral plate and thus the long-term survival of the repair tissue after ACT.
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  • Virtanen, Ismo, et al. (author)
  • Blood vessels of human islets of Langerhans are surrounded by a double basement membrane
  • 2008
  • In: Diabetologia. - : Springer Science and Business Media LLC. - 0012-186X .- 1432-0428. ; 51:7, s. 1181-91
  • Journal article (peer-reviewed)abstract
    • AIMS/HYPOTHESIS: Based on mouse study findings, pancreatic islet cells are supposed to lack basement membrane (BM) and interact directly with vascular endothelial BM. Until now, the BM composition of human islets has remained elusive. METHODS: Immunohistochemistry with specific monoclonal and polyclonal antibodies as well as electron microscopy were used to study BM organisation and composition in human adult islets. Isolated islet cells and function-blocking monoclonal antibodies and recombinant soluble Lutheran peptide were further used to study islet cell adhesion to laminin (Lm)-511. Short-term cultures of islets were used to study Lutheran and integrin distribution. RESULTS: Immunohistochemistry revealed a unique organisation for human Lm-511/521 as a peri-islet BM, which co-invaginated into islets with vessels, forming an outer endocrine BM of the intra-islet vascular channels, and was distinct from the vascular BM that additionally contained Lm-411/421. These findings were verified by electron microscopy. Lutheran glycoprotein, a receptor for the Lm alpha5 chain, was found prominently on endocrine cells, as identified by immunohistochemistry and RT-PCR, whereas alpha(3) and beta(1) integrins were more diffusely distributed. High Lutheran content was also found on endocrine cell membranes in short-term culture of human islets. The adhesion of dispersed beta cells to Lm-511 was inhibited equally effectively by antibodies to integrin and alpha(3) and beta(1) subunits, and by soluble Lutheran peptide. CONCLUSIONS/INTERPRETATION: The present results disclose a hitherto unrecognised BM organisation and adhesion mechanisms in human pancreatic islets as distinct from mouse islets.
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