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      Akkermansia muciniphila-derived extracellular vesicles influence gut permeability through the regulation of tight junctions

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          Abstract

          The gut microbiota has an important role in the gut barrier, inflammation and metabolic functions. Studies have identified a close association between the intestinal barrier and metabolic diseases, including obesity and type 2 diabetes (T2D). Recently, Akkermansia muciniphila has been reported as a beneficial bacterium that reduces gut barrier disruption and insulin resistance. Here we evaluated the role of A. muciniphila-derived extracellular vesicles (AmEVs) in the regulation of gut permeability. We found that there are more AmEVs in the fecal samples of healthy controls compared with those of patients with T2D. In addition, AmEV administration enhanced tight junction function, reduced body weight gain and improved glucose tolerance in high-fat diet (HFD)-induced diabetic mice. To test the direct effect of AmEVs on human epithelial cells, cultured Caco-2 cells were treated with these vesicles. AmEVs decreased the gut permeability of lipopolysaccharide-treated Caco-2 cells, whereas Escherichia coli-derived EVs had no significant effect. Interestingly, the expression of occludin was increased by AmEV treatment. Overall, these results imply that AmEVs may act as a functional moiety for controlling gut permeability and that the regulation of intestinal barrier integrity can improve metabolic functions in HFD-fed mice.

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          Most cited references37

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          Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication.

          Normal and malignant cells shed from their surface membranes as well as secrete from the endosomal membrane compartment circular membrane fragments called microvesicles (MV). MV that are released from viable cells are usually smaller in size compared to the apoptotic bodies derived from damaged cells and unlike them do not contain fragmented DNA. Growing experimental evidence indicates that MV are an underappreciated component of the cell environment and play an important pleiotropic role in many biological processes. Generally, MV are enriched in various bioactive molecules and may (i) directly stimulate cells as a kind of 'signaling complex', (ii) transfer membrane receptors, proteins, mRNA and organelles (e.g., mitochondria) between cells and finally (iii) deliver infectious agents into cells (e.g., human immuno deficiency virus, prions). In this review, we discuss the pleiotropic effects of MV that are important for communication between cells, as well as the role of MV in carcinogenesis, coagulation, immune responses and modulation of susceptibility/infectability of cells to retroviruses or prions.
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            Exosomes: secreted vesicles and intercellular communications

            Exosomes are small membrane vesicles of endocytic origin secreted by most cell types, and are thought to play important roles in intercellular communications. Although exosomes were originally described in 1983, interest in these vesicles has really increased dramatically in the last 3 years, after the finding that they contain mRNA and microRNA. This discovery sparked renewed interest for the general field of membrane vesicles involved in intercellular communications, and research on these structures has grown exponentially over the last few years, probing their composition and function, as well as their potential value as biomarkers.
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              Microbes inside--from diversity to function: the case of Akkermansia.

              The human intestinal tract is colonized by a myriad of microbes that have developed intimate interactions with the host. In healthy individuals, this complex ecosystem remains stable and resilient to stressors. There is significant attention on the understanding of the composition and function of this intestinal microbiota in health and disease. Current developments in metaomics and systems biology approaches allow to probe the functional potential and activity of the intestinal microbiota. However, all these approaches inherently suffer from the fact that the information on macromolecules (DNA, RNA and protein) is collected at the ecosystem level. Similarly, all physiological and other information collected from isolated strains relates to pure cultures grown in vitro or in gnotobiotic systems. It is essential to integrate these two worlds of predominantly chemistry and biology by linking the molecules to the cells. Here, we will address the integration of omics- and culture-based approaches with the complexity of the human intestinal microbiota in mind and the mucus-degrading bacteria Akkermansia spp. as a paradigm.
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                Author and article information

                Journal
                Exp Mol Med
                Exp. Mol. Med
                Experimental & Molecular Medicine
                Nature Publishing Group
                1226-3613
                2092-6413
                February 2018
                23 February 2018
                1 February 2018
                : 50
                : 2
                : e450
                Affiliations
                [1 ]Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology , Pohang, Republic of Korea
                [2 ]Department of Life Sciences, Pohang University of Science and Technology (POSTECH) , Pohang, Republic of Korea
                [3 ]NovaCell Technology Inc. , Pohang, Republic of Korea
                [4 ]Asan Institute of Life Sciences, University of Ulsan College of Medicine , Seoul, Republic of Korea
                [5 ]Department of Internal Medicine, Dankook University College of Medicine , Cheonan, Republic of Korea
                [6 ]Department of Allergy and Clinical Immunology, Ajou University School of Medicine , Suwon-si, Republic of Korea
                [7 ]MD Healthcare Inc. , Seoul, Republic of Korea
                Author notes
                [* ]MD Healthcare Inc., 9 World Cup buk-ro, 56-gil, Mapo-gu , Seoul 03923, Republic of Korea. E-mail: ykkim@ 123456mdhc.kr
                [* ]Department of Life Sciences, Pohang University of Science and Technology, POSTECH Biotech Center , Pohang, Gyeongbuk 37673, Republic of Korea. E-mail: sungho@ 123456postech.ac.kr
                [8]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0001-8413-5006
                http://orcid.org/0000-0003-3366-2345
                Article
                emm2017282
                10.1038/emm.2017.282
                5903829
                29472701
                59ba55fc-06e3-4f2a-bf6b-684371646b26
                Copyright © 2018 The Author(s)

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/

                History
                : 04 July 2017
                : 09 September 2017
                : 11 September 2017
                Categories
                Original Article

                Molecular medicine
                Molecular medicine

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