47 research outputs found

    Regulatory T cell-derived extracellular vesicles modify dendritic cell function

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    Regulatory T cells (Treg) are a subpopulation of T cells that maintain tolerance to self and limit other immune responses. They achieve this through different mechanisms including the release of extracellular vesicles (EVs) such as exosomes as shown by us, and others. One of the ways that Treg derived EVs inhibit target cells such as effector T cells is via the transfer of miRNA. Another key target for the immunoregulatory function of Tregs is the dendritic cells (DCs). In this study we demonstrate directly, and for the first time, that miRNAs are transferred from Tregs to DCs via Treg derived EVs. In particular two miRNAs, namely miR-150-5p and miR-142-3p, were increased in DCs following their interaction with Tregs and Treg derived exosomes. One of the consequences for DCs following the acquisition of miRNAs contained in Treg derived EVs was the induction of a tolerogenic phenotype in these cells, with increased IL-10 and decreased IL-6 production being observed following LPS stimulation. Altogether our findings provide data to support the idea that intercellular transfer of miRNAs via EVs may be a novel mechanism by which Tregs regulate DC function and could represent a mechanism to inhibit immune reactions in tissues

    Therapeutic application of T regulatory cells in composite tissue allotransplantation

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    Emulsion Templated Scaffolds with Tunable Mechanical Properties for Bone Tissue Engineering

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    Polymerised High Internal Phase Emulsions (PolyHIPEs) are manufactured via emulsion templating and exhibit a highly interconnected microporosity. These materials are commonly used as thin membranes for 3D cell culture. This study uses emulsion templating in combination with microstereolithography to fabricate PolyHIPE scaffolds with a tightly controlled and reproducible architecture. This combination of methods produces hierarchical structures, where the microstructural properties can be independently controlled from the scaffold macrostructure. PolyHIPEs were fabricated with varying ratios of two acrylate monomers (2-ethylhexyl acrylate (EHA) and isobornyl acrylate (IBOA)) and varying nominal porosity to tune mechanical properties. Young's modulus, ultimate tensile stress (UTS) and elongation at failure were determined for twenty EHA/IBOA compositions. Moduli ranged from 63.01±9.13 to 0.36±0.04MPa, UTS from 2.03±0.33 to 0.11±0.01MPa and failure strain from 21.86±2.87% to 2.60±0.61%. Selected compositions were fabricated into macro-porous woodpile structures, plasma treated with air or acrylic acid and seeded with human embryonic stem-cell derived mesenchymal progenitor cells (hES-MPs). Confocal and two-photon microscopy confirmed cell proliferation and penetration into the micro- and macro-porous architecture. The scaffolds supported osteogenic differentiation of mesenchymal cells and interestingly, the stiffest IBOA-based scaffolds that were plasma treated with acrylic acid promoted osteogenesis more strongly than the other scaffolds

    What Is Direct Allorecognition?

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    Direct allorecognition is the process by which donor-derived major histocompatibility complex (MHC)-peptide complexes, typically presented by donor-derived ‘passenger’ dendritic cells, are recognised directly by recipient T cells. In this review, we discuss the two principle theories which have been proposed to explain why individuals possess a high-precursor frequency of T cells with direct allospecificity and how self-restricted T cells recognise allogeneic MHCpeptide complexes. These theories, both of which are supported by functional and structural data, suggest that T cells recognising allogeneic MHC-peptide complexes focus either on the allopeptides bound to the allo-MHC molecules or the allo-MHC molecules themselves. We discuss how direct alloimmune responses may be sustained long term, the consequences of this for graft outcome and highlight novel strategies which are currently being investigated as a potential means of reducing rejection mediated through this pathway

    Generation of optimized datapaths: bit-slice versus standard cells

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    INTERNATIONAL STANDARD SERIAL NUMBERS (Translation and Original): 0926-5473In some CAD systems, the implementation of regular or semi-regular datapaths is eased by providing specific tools, called `datapath compilers'. These tools take advantage of the regularity in the datapath specification and generally use a bit-slice structure for the implementation. In other systems, no specific tool is provided and the datapaths are implemented using classical standard cell place and route tools. The authors propose metrics for both evaluating the interest of using datapath compilers and comparing the effectiveness of different tools. Some experiments on a commercially available datapath compiler demonstrate that a standard cell implementation is less efficient, at least for two-level metal technologies

    Clocking scheme selection for circuits made up of a controller and a datapath

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    Various optimizations and trade-offs have been implemented in synthesis systems. However, the clocking scheme selection was generally not considered. Several schemes are presented to address the different types of circuits made up of a controller and a datapath. The selection of one of these schemes, according to the characteristics of the two blocks, is discussed and a practical example demonstrates the impact that this selection has on the final circuit characteristics

    Taking advantage of high level functional information to refine timing analysis and timing information

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    ISBN: 0818654104High level functional information, available in a circuit specification, can be used to refine timing analysis or modeling. The notion of functional false path is first introduced. Then, the principles of an accurate timing analysis are presented for circuits made up of a controller and a datapath. The approach takes advantage of the circuit hierarchy to reduce the computation complexity and avoids reporting functional false paths
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