13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Immunostimulatory Effects Triggered by Enterococcus faecalis CECT7121 Probiotic Strain Involve Activation of Dendritic Cells and Interferon-Gamma Production

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Probiotics can modulate the immune system, conferring beneficial effects on the host. Understanding how these microorganisms contribute to improve the health status is still a challenge. Previously, we have demonstrated that Enterococcus faecalis CECT7121 implants itself and persists in the murine gastrointestinal tract, and enhances and skews the profile of cytokines towards the Th1 phenotype in several biological models. Given the importance of dendritic cells (DCs) in the orchestration of immunity, the aim of this work was to elucidate the influence of E. faecalis CECT7121 on DCs and the outcome of the immune responses. In this work we show that E. faecalis CECT7121 induces a strong dose-dependent activation of DCs and secretion of high levels of IL-12, IL-6, TNFα, and IL-10. This stimulation is dependent on TLR signaling, and skews the activation of T cells towards the production of IFNγ. The influence of this activation in the establishment of Th responses in vivo shows the accumulation of specific IFNγ-producing cells. Our findings indicate that the activation exerted by E. faecalis CECT7121 on DCs and its consequence on the cellular adaptive immune response may have broad therapeutic implications in immunomodulation.

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: not found

          Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function.

          MyD88, originally isolated as a myeloid differentiation primary response gene, is shown to act as an adaptor in interleukin-1 (IL-1) signaling by interacting with both the IL-1 receptor complex and IL-1 receptor-associated kinase (IRAK). Mice generated by gene targeting to lack MyD88 have defects in T cell proliferation as well as induction of acute phase proteins and cytokines in response to IL-1. Increases in interferon-gamma production and natural killer cell activity in response to IL-18 are abrogated. In vivo Th1 response is also impaired. Furthermore, IL-18-induced activation of NF-kappaB and c-Jun N-terminal kinase (JNK) is blocked in MyD88-/- Th1-developing cells. Taken together, these results demonstrate that MyD88 is a critical component in the signaling cascade that is mediated by IL-1 receptor as well as IL-18 receptor.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Defective TCR expression in transgenic mice constructed using cDNA-based alpha- and beta-chain genes under the control of heterologous regulatory elements.

            We describe the generation of ovalbumin (OVA)-specific, MHC class II-restricted alpha beta T cell receptor (TCR) transgenic mice. Initial attempts at generating these transgenic mice utilized heterologous regulatory elements to drive the expression of cDNA genes encoding the separate alpha- and beta-chains of the TCR. Unexpectedly, T cells bearing the transgenic alpha beta TCR failed to emerge from the thymus in these mice, although the transgenes did modify endogenous TCR expression. However, subsequent modification of the approach which enabled expression of the TCR beta-chain under the control of its natural regulatory elements generated mice whose peripheral T cells expressed the transgenic TCR and were capable of antigen-dependent proliferation. These results show that successful generation of MHC class II-restricted, OVA-specific alpha beta TCR transgenic mice was dependent upon combining cDNA- and genomic DNA-based constructs for expression of the respective alpha- and beta-chains of the TCR.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Differential antigen processing by dendritic cell subsets in vivo.

              Dendritic cells (DCs) process and present self and foreign antigens to induce tolerance or immunity. In vitro models suggest that induction of immunity is controlled by regulating the presentation of antigen, but little is known about how DCs control antigen presentation in vivo. To examine antigen processing and presentation in vivo, we specifically targeted antigens to two major subsets of DCs by using chimeric monoclonal antibodies. Unlike CD8+ DCs that express the cell surface protein CD205, CD8- DCs, which are positive for the 33D1 antigen, are specialized for presentation on major histocompatibility complex (MHC) class II. This difference in antigen processing is intrinsic to the DC subsets and is associated with increased expression of proteins involved in MHC processing.
                Bookmark

                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                15 May 2015
                2015
                : 10
                : 5
                : e0127262
                Affiliations
                [1 ]Laboratorio de Modulación de la Respuesta Inmune, IDEHU (CONICET-UBA). Ciudad Autónoma de Buenos Aires, Argentina
                [2 ]Institute of Infection Immunology, TWINCORE, Centre for Experimental and Clinical Infection Research, a Joint Venture between the Medical School Hanover (MHH) and the Helmholtz Centre for Infection Research (HZI), Hannover, Germany
                [3 ]Instituto de Inmunología, Genética y Metabolismo, INIGEM (CONICET-UBA). Ciudad Autónoma de Buenos Aires, Argentina
                [4 ]Laboratorio de Anticuerpos Asimétricos e Inmunología de la Reproducción, IDEHU (CONICET-UBA). Ciudad Autónoma de Buenos Aires, Argentina
                Institut National de la Santé et de la Recherche Médicale (INSERM), FRANCE
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MAM TS LB MSC MarAM. Performed the experiments: MAM AMD CH WG MVG GGN AMC MSC. Analyzed the data: MAM LB MSC. Contributed reagents/materials/analysis tools: TS MSC MarAM. Wrote the paper: MAM CH WG GGN TS LB MSC MarAM.

                Article
                PONE-D-14-54768
                10.1371/journal.pone.0127262
                4433276
                25978357
                df1b0e0c-d1aa-4bce-b2e0-a9ab96b490ad
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 6 December 2014
                : 14 April 2015
                Page count
                Figures: 9, Tables: 3, Pages: 20
                Funding
                Our work was partly supported by University of Buenos Aires, Argentina (grant number 20020100101002) to MarAM and institutional funding from the Institute of Infection Immunology (Twincore, Hannover, Germany). This work was done in the frame of a scientific collaborative program (PROALAR DA/10/05) between the Institute of Infection Immunology (Twincore, Hannover, Germany) and the Laboratorio de Modulación de la Respuesta Inmune, (IDEHU,CONICET-UBA, Argentina) granted to TDS and MarAM by the Ministry of Science, Technology and Productive Innovation (MINCyT, Argentina) and the German Academic Exchange Service (DAAD, Germany). The funds granted by this program were exclusively aimed to cover the costs of travel and accommodations for travel between Germany and Argentina for the researchers involved to specific project tasks. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
                Categories
                Research Article
                Custom metadata
                All relevant data are within the paper.

                Uncategorized
                Uncategorized

                Comments

                Comment on this article