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      Polysaccharide from wheat bran induces cytokine expression via the toll-like receptor 4-mediated p38 MAPK signaling pathway and prevents cyclophosphamide-induced immunosuppression in mice

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          ABSTRACT

          Wheat bran-derived polysaccharides have attracted particular attention due to their immunomodulatory effects. However, the molecular mechanisms underlying their functions are poorly understood. The current study was designed to examine the effect of wheat bran polysaccharide (WBP) on RAW 264.7 cells and the underlying signaling pathways, which have not been explored. In addition, we also investigated the immuno-enhancement effects of WBP on cyclophosphamide (CTX)-induced immunosuppression in mice. WBP significantly increased the concentrations of intracellular nitric oxide (NO) and cytokines such as prostaglandin E 2 (PGE 2) and tumor necrosis factor-α (TNF-α) in RAW 264.7 cells. The result of RT-PCR analysis indicated that WBP also enhanced inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and TNF-α expression. Further analyses demonstrated that WBP rapidly activated phosphorylated p38 mitogen-activated protein kinase (MAPK) and the transcriptional activities of activator protein-1 (AP-1) and nuclear factor (NF)-κB via toll-like receptor 4 (TLR4). Furthermore, in vivo experiments revealed that WBP increased the spleen and thymus indices significantly, and markedly promoted the production of the serum cytokines IL-2 and IFN-γ in CTX-induced immunosuppressed mice. Taken together, these results suggest that WBP can improve immunity by enhancing immune function, and could be explored as a potential immunomodulatory agent in functional food.

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          Immunogenic cell death in cancer and infectious disease

          Initiation of an adaptive immune response depends on the detection of both antigenic epitopes and adjuvant signals. Infectious pathogens and cancer cells often avoid immune detection by limiting the release of danger signals from dying cells. When is cell death immunogenic and what are the pathophysiological implications of this process?
            Bookmark
            • Record: found
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            • Article: not found

            Inflammatory and immune pathways in the pathogenesis of periodontal disease.

            The pathogenesis of periodontitis involves a complex immune/inflammatory cascade that is initiated by the bacteria of the oral biofilm that forms naturally on the teeth. The susceptibility to periodontitis appears to be determined by the host response; specifically, the magnitude of the inflammatory response and the differential activation of immune pathways. The purpose of this review was to delineate our current knowledge of the host response in periodontitis. The role of innate immunity, the failure of acute inflammation to resolve (thus becoming chronic), the cytokine pathways that regulate the activation of acquired immunity and the cells and products of the immune system are considered. New information relating to regulation of both inflammation and the immune response will be reviewed in the context of susceptibility to, and perhaps control of, periodontitis. © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
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              • Abstract: found
              • Article: not found

              A review of the molecular aspects of melatonin's anti-inflammatory actions: recent insights and new perspectives.

              Melatonin is a highly evolutionary conserved endogenous molecule that is mainly produced by the pineal gland, but also by other nonendocrine organs, of most mammals including man. In the recent years, a variety of anti-inflammatory and antioxidant effects have been observed when melatonin is applied exogenously under both in vivo and in vitro conditions. A number of studies suggest that this indole may exert its anti-inflammatory effects through the regulation of different molecular pathways. It has been documented that melatonin inhibits the expression of the isoforms of inducible nitric oxide synthase and cyclooxygenase and limits the production of excessive amounts of nitric oxide, prostanoids, and leukotrienes, as well as other mediators of the inflammatory process such as cytokines, chemokines, and adhesion molecules. Melatonin's anti-inflammatory effects are related to the modulation of a number of transcription factors such as nuclear factor kappa B, hypoxia-inducible factor, nuclear factor erythroid 2-related factor 2, and others. Melatonin's effects on the DNA-binding capacity of transcription factors may be regulated through the inhibition of protein kinases involved in signal transduction, such as mitogen-activated protein kinases. This review summarizes recent research data focusing on the modulation of the expression of different inflammatory mediators by melatonin and the effects on cell signaling pathways responsible for the indole's anti-inflammatory activity. Although there are a numerous published reports that have analyzed melatonin's anti-inflammatory properties, further studies are necessary to elucidate its complex regulatory mechanisms in different cellular types and tissues. © 2012 John Wiley & Sons A/S.
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                Author and article information

                Journal
                Food Nutr Res
                Food Nutr Res
                ZFNR
                zfnr20
                Food & Nutrition Research
                Taylor & Francis
                1654-661X
                2017
                9 July 2017
                : 61
                : 1
                : 1344523
                Affiliations
                [ a ] Jiangsu Collaborative Innovation Center of Regional Modern Agriculture & Environmental protection/Jiangsu Key Laboratory for Eco-Agricultural Biotechnology around Hongze Lake, Huaiyin Normal University , Huaian, PR China
                [ b ] Department of Urology, Huai’an First People’s Hospital, Nanjing Medical University , Huaian, PR China
                [ c ] School of Life Science and Engineering, Lanzhou University of Technology , Lanzhou, PR China
                [ d ] Huaiyin Institute of Agricultural Science of Xuhuai Region , Huaian, PR China
                Author notes
                CONTACT Xiangxiang Zhao xxzhao2013@ 123456163.com
                [*]

                These authors contributed equally to this work

                Article
                1344523
                10.1080/16546628.2017.1344523
                5510218
                fd16cd7c-e6e3-4b9b-871d-ffe028b84d28
                © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 March 2017
                : 15 June 2017
                Page count
                Figures: 6, Tables: 5, References: 53, Pages: 13
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 31600281
                Funded by: Natural Science Foundation of Jiangsu Province 10.13039/501100004608
                Award ID: BK20150414
                Funded by: Top-notch Academic Programs Project of Jiangsu Higher Education Institutions
                Award ID: PPZY2015A018
                Funded by: Natural Science Foundation of the Higher Education Institutions of Jiangsu Province
                Award ID: 15KJB550001
                Funded by: Natural Science Foundation of the Higher Education Institutions of Jiangsu Province
                Award ID: 14KJB550002
                Funded by: Qing Lan Project of Jiangsu Province
                Award ID: 2016
                This study was supported financially by Natural Science Foundation of Jiangsu Province [BK20150414], Natural Science Foundation of the Higher Education Institutions of Jiangsu Province [14KJB550002 and 15KJB550001], National Natural Science Foundation of China [31600281], Top-notch Academic Programs Project of Jiangsu Higher Education Institutions [PPZY2015A018], and Qing Lan Project of Jiangsu Province.
                Categories
                Article
                Original Article

                Nutrition & Dietetics
                wheat bran polysaccharide,immunomodulatory activity,raw 264.7 macrophages,toll-like receptor 4

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