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      Extracellular Vesicles with Possible Roles in Gut Intestinal Tract Homeostasis and IBD

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          Abstract

          The intestinal tract consists of various types of cells, such as epithelial cells, Paneth cells, macrophages, and lymphocytes, which constitute the intestinal immune system and play a significant role in maintaining intestinal homeostasis by producing antimicrobial materials and controlling the host-commensal balance. Various studies have found that the dysfunction of intestinal homeostasis contributes to the pathogenesis of inflammatory bowel disease (IBD). As a novel mediator, extracellular vesicles (EVs) have been recognized as effective communicators, not only between cells but also between cells and the organism. In recent years, EVs have been regarded as vital characters for dysregulated homeostasis and IBD in either the etiology or the pathology of intestinal inflammation. Here, we review recent studies on EVs associated with intestinal homeostasis and IBD and discuss their source, cargo, and origin, as well as their therapeutic effects on IBD, which mainly include artificial nanoparticles and EVs derived from microorganisms.

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          Most cited references103

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          Biogenesis and secretion of exosomes.

          Although observed for several decades, the release of membrane-enclosed vesicles by cells into their surrounding environment has been the subject of increasing interest in the past few years, which led to the creation, in 2012, of a scientific society dedicated to the subject: the International Society for Extracellular Vesicles. Convincing evidence that vesicles allow exchange of complex information fuelled this rise in interest. But it has also become clear that different types of secreted vesicles co-exist, with different intracellular origins and modes of formation, and thus probably different compositions and functions. Exosomes are one sub-type of secreted vesicles. They form inside eukaryotic cells in multivesicular compartments, and are secreted when these compartments fuse with the plasma membrane. Interestingly, different families of molecules have been shown to allow intracellular formation of exosomes and their subsequent secretion, which suggests that even among exosomes different sub-types exist. Copyright © 2014 Elsevier Ltd. All rights reserved.
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            Annexin A1 and glucocorticoids as effectors of the resolution of inflammation.

            Glucocorticoids are widely used for the management of inflammatory diseases. Their clinical application stems from our understanding of the inhibitory effect of the corticosteroid hormone cortisol on several components of the immune system. Endogenous and exogenous glucocorticoids mediate their multiple anti-inflammatory effects through many effector molecules. In this Opinion article, we focus on the role of one such effector molecule, annexin A1, and summarize the recent studies that provide insight into its molecular and pharmacological functions in immune responses. In addition, we propose a model in which glucocorticoids regulate the expression and function of annexin A1 in opposing ways in innate and adaptive immune cells to mediate the resolution of inflammation.
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              Gram-positive bacteria produce membrane vesicles: proteomics-based characterization of Staphylococcus aureus-derived membrane vesicles.

              Although archaea, Gram-negative bacteria, and mammalian cells constitutively secrete membrane vesicles (MVs) as a mechanism for cell-free intercellular communication, this cellular process has been overlooked in Gram-positive bacteria. Here, we found for the first time that Gram-positive bacteria naturally produce MVs into the extracellular milieu. Further characterizations showed that the density and size of Staphylococcus aureus-derived MVs are both similar to those of Gram-negative bacteria. With a proteomics approach, we identified with high confidence a total of 90 protein components of S. aureus-derived MVs. In the group of identified proteins, the highly enriched extracellular proteins suggested that a specific sorting mechanism for vesicular proteins exists. We also identified proteins that facilitate the transfer of proteins to other bacteria, as well to eliminate competing organisms, antibiotic resistance, pathological functions in systemic infections, and MV biogenesis. Taken together, these observations suggest that the secretion of MVs is an evolutionally conserved, universal process that occurs from simple organisms to complex multicellular organisms. This information will help us not only to elucidate the biogenesis and functions of MVs, but also to develop therapeutic tools for vaccines, diagnosis, and antibiotics effective against pathogenic strains of Gram-positive bacteria.
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                Author and article information

                Contributors
                Journal
                Mediators Inflamm
                Mediators Inflamm
                MI
                Mediators of Inflammation
                Hindawi
                0962-9351
                1466-1861
                2020
                13 January 2020
                : 2020
                : 1945832
                Affiliations
                1Department of Gastroenterology, Gongli Hospital, The Second Military Medical University, Shanghai, China
                2Department of Gastroenterology, Changhai Hospital, Second Military Medical University/Naval Medical University, Shanghai, China
                3Department of Gastroenterology, The Second Clinical Medical College, Jinan University, Shenzhen, China
                Author notes

                Academic Editor: Soh Yamazaki

                Author information
                https://orcid.org/0000-0002-3472-1602
                https://orcid.org/0000-0003-0404-242X
                https://orcid.org/0000-0002-7577-6001
                Article
                10.1155/2020/1945832
                7201673
                b092f5a1-f4da-4949-8cf0-de040b4e7ad4
                Copyright © 2020 Xin Chang et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 September 2019
                : 17 December 2019
                : 24 December 2019
                Funding
                Funded by: Science and Technology Development Fund of Shanghai Pudong New Area
                Award ID: PKJ2016-Y15
                Funded by: Technical Research and Development Project of Shenzhen
                Award ID: JCYJ20170307100538697
                Award ID: JCYJ20150403101028164
                Funded by: Three Engineering Training Funds in Shenzhen
                Award ID: SYLY201718
                Funded by: Shanghai Education Development Foundation
                Award ID: 19SG30
                Funded by: Shanghai Municipal Education Commission
                Funded by: National Natural Science Foundation of China
                Award ID: 81800489
                Award ID: 81873546
                Award ID: 81670473
                Funded by: National Key R&D Program of China
                Award ID: 2018YFC1313103
                Award ID: 2017YFC1308800
                Categories
                Review Article

                Immunology
                Immunology

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