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      Exosomes in brain diseases: Pathogenesis and therapeutic targets

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          Abstract

          Exosomes are extracellular vesicles with diameters of about 100 nm that are naturally secreted by cells into body fluids. They are derived from endosomes and are wrapped in lipid membranes. Exosomes are involved in intracellular metabolism and intercellular communication. They contain nucleic acids, proteins, lipids, and metabolites from the cell microenvironment and cytoplasm. The contents of exosomes can reflect their cells’ origin and allow the observation of tissue changes and cell states under disease conditions. Naturally derived exosomes have specific biomolecules that act as the “fingerprint” of the parent cells, and the contents changed under pathological conditions can be used as biomarkers for disease diagnosis. Exosomes have low immunogenicity, are small in size, and can cross the blood–brain barrier. These characteristics make exosomes unique as engineering carriers. They can incorporate therapeutic drugs and achieve targeted drug delivery. Exosomes as carriers for targeted disease therapy are still in their infancy, but exosome engineering provides a new perspective for cell‐free disease therapy. This review discussed exosomes and their relationship with the occurrence and treatment of some neuropsychiatric diseases. In addition, future applications of exosomes in the diagnosis and treatment of neuropsychiatric disorders were evaluated in this review.

          Abstract

          Exosomes from neural cells can cross the blood–brain barrier, which can be used for diagnosis. Meanwhile, exosomes can be modified and engineered by loading specific nucleic acids, proteins, and drugs, which can be peripherally injected and play a therapeutic role to restore the health of the brain.

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          The biology, function, and biomedical applications of exosomes

          The study of extracellular vesicles (EVs) has the potential to identify unknown cellular and molecular mechanisms in intercellular communication and in organ homeostasis and disease. Exosomes, with an average diameter of ~100 nanometers, are a subset of EVs. The biogenesis of exosomes involves their origin in endosomes, and subsequent interactions with other intracellular vesicles and organelles generate the final content of the exosomes. Their diverse constituents include nucleic acids, proteins, lipids, amino acids, and metabolites, which can reflect their cell of origin. In various diseases, exosomes offer a window into altered cellular or tissue states, and their detection in biological fluids potentially offers a multicomponent diagnostic readout. The efficient exchange of cellular components through exosomes can inform their applied use in designing exosome-based therapeutics.
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            Shedding light on the cell biology of extracellular vesicles

            Extracellular vesicles are a heterogeneous group of cell-derived membranous structures comprising exosomes and microvesicles, which originate from the endosomal system or which are shed from the plasma membrane, respectively. They are present in biological fluids and are involved in multiple physiological and pathological processes. Extracellular vesicles are now considered as an additional mechanism for intercellular communication, allowing cells to exchange proteins, lipids and genetic material. Knowledge of the cellular processes that govern extracellular vesicle biology is essential to shed light on the physiological and pathological functions of these vesicles as well as on clinical applications involving their use and/or analysis. However, in this expanding field, much remains unknown regarding the origin, biogenesis, secretion, targeting and fate of these vesicles.
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              Extracellular vesicles: Exosomes, microvesicles, and friends

              Cells release into the extracellular environment diverse types of membrane vesicles of endosomal and plasma membrane origin called exosomes and microvesicles, respectively. These extracellular vesicles (EVs) represent an important mode of intercellular communication by serving as vehicles for transfer between cells of membrane and cytosolic proteins, lipids, and RNA. Deficiencies in our knowledge of the molecular mechanisms for EV formation and lack of methods to interfere with the packaging of cargo or with vesicle release, however, still hamper identification of their physiological relevance in vivo. In this review, we focus on the characterization of EVs and on currently proposed mechanisms for their formation, targeting, and function.
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                Author and article information

                Contributors
                jiangpeicsu@sina.com
                Journal
                MedComm (2020)
                MedComm (2020)
                10.1002/(ISSN)2688-2663
                MCO2
                MedComm
                John Wiley and Sons Inc. (Hoboken )
                2688-2663
                11 June 2023
                June 2023
                : 4
                : 3 ( doiID: 10.1002/mco2.v4.3 )
                : e287
                Affiliations
                [ 1 ] Department of Endocrinology Tengzhou Central People's Hospital Tengzhou China
                [ 2 ] Department of Oncology Tengzhou Central People's Hospital Tengzhou China
                [ 3 ] Translational Pharmaceutical Laboratory Jining First People's Hospital Shandong First Medical University Jining China
                [ 4 ] Institute of Translational Pharmacy Jining Medical Research Academy Jining China
                Author notes
                [*] [* ] Correspondence

                Pei Jiang, Translational Pharmaceutical Laboratory, Jining First People's Hospital, Shandong First Medical University, Jining 272000, China; Institute of Translational Pharmacy, Jining Medical Research Academy, Jining 272000, China.

                Email: jiangpeicsu@ 123456sina.com

                [#]

                Qingying Si and Linlin Wu contributed equally to this work.

                Article
                MCO2287
                10.1002/mco2.287
                10258444
                37313330
                0e0da86d-93c5-4697-acae-157ae76b86da
                © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 April 2023
                : 19 December 2022
                : 08 May 2023
                Page count
                Figures: 5, Tables: 3, Pages: 26, Words: 16783
                Funding
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: 81602846
                Award ID: 82272253
                Funded by: Natural Science Foundation of Shandong Province , doi 10.13039/501100007129;
                Award ID: ZR2021MH145
                Funded by: Taishan Scholar Project of Shandong Province , doi 10.13039/501100010040;
                Award ID: tsqn201812159
                Funded by: China International Medical Foundation , doi 10.13039/501100014764;
                Award ID: Z‐2018‐35‐2002
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                June 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.9 mode:remove_FC converted:12.06.2023

                biomarker,diagnosis,exosomes,neuropsychiatric diseases,treatment

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