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      Guidelines for the purification and characterization of extracellular vesicles of parasites

      1 , 2 , 3 , 4 , 5 , 6 , 1 , 7 , 8 , 1 , 4 , 1 , 5 , 4 , 4 , 9 , 10 , 11 , 8 , 12 , 13 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 1 , 2 , 21 , 5 , 22 , 23 , 6 , 4
      Journal of Extracellular Biology
      Wiley

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          Abstract

          Parasites are responsible for the most neglected tropical diseases, affecting over a billion people worldwide (WHO, 2015) and accounting for billions of cases a year and responsible for several millions of deaths. Research on extracellular vesicles (EVs) has increased in recent years and demonstrated that EVs shed by pathogenic parasites interact with host cells playing an important role in the parasite's survival, such as facilitation of infection, immunomodulation, parasite adaptation to the host environment and the transfer of drug resistance factors. Thus, EVs released by parasites mediate parasite‐parasite and parasite‐host intercellular communication. In addition, they are being explored as biomarkers of asymptomatic infections and disease prognosis after drug treatment. However, most current protocols used for the isolation, size determination, quantification and characterization of molecular cargo of EVs lack greater rigor, standardization, and adequate quality controls to certify the enrichment or purity of the ensuing bioproducts. We are now initiating major guidelines based on the evolution of collective knowledge in recent years. The main points covered in this position paper are methods for the isolation and molecular characterization of EVs obtained from parasite‐infected cell cultures, experimental animals, and patients. The guideline also includes a discussion of suggested protocols and functional assays in host cells

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          Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

          ABSTRACT The last decade has seen a sharp increase in the number of scientific publications describing physiological and pathological functions of extracellular vesicles (EVs), a collective term covering various subtypes of cell-released, membranous structures, called exosomes, microvesicles, microparticles, ectosomes, oncosomes, apoptotic bodies, and many other names. However, specific issues arise when working with these entities, whose size and amount often make them difficult to obtain as relatively pure preparations, and to characterize properly. The International Society for Extracellular Vesicles (ISEV) proposed Minimal Information for Studies of Extracellular Vesicles (“MISEV”) guidelines for the field in 2014. We now update these “MISEV2014” guidelines based on evolution of the collective knowledge in the last four years. An important point to consider is that ascribing a specific function to EVs in general, or to subtypes of EVs, requires reporting of specific information beyond mere description of function in a crude, potentially contaminated, and heterogeneous preparation. For example, claims that exosomes are endowed with exquisite and specific activities remain difficult to support experimentally, given our still limited knowledge of their specific molecular machineries of biogenesis and release, as compared with other biophysically similar EVs. The MISEV2018 guidelines include tables and outlines of suggested protocols and steps to follow to document specific EV-associated functional activities. Finally, a checklist is provided with summaries of key points.
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            An improved technique for determining hardness and elastic modulus using load and displacement sensing indentation experiments

            The indentation load-displacement behavior of six materials tested with a Berkovich indenter has been carefully documented to establish an improved method for determining hardness and elastic modulus from indentation load-displacement data. The materials included fused silica, soda–lime glass, and single crystals of aluminum, tungsten, quartz, and sapphire. It is shown that the load–displacement curves during unloading in these materials are not linear, even in the initial stages, thereby suggesting that the flat punch approximation used so often in the analysis of unloading data is not entirely adequate. An analysis technique is presented that accounts for the curvature in the unloading data and provides a physically justifiable procedure for determining the depth which should be used in conjunction with the indenter shape function to establish the contact area at peak load. The hardnesses and elastic moduli of the six materials are computed using the analysis procedure and compared with values determined by independent means to assess the accuracy of the method. The results show that with good technique, moduli can be measured to within 5%.
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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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                Journal
                Journal of Extracellular Biology
                J of Extracellular Bio
                Wiley
                2768-2811
                2768-2811
                October 2023
                October 19 2023
                October 2023
                : 2
                : 10
                Affiliations
                [1 ] ISGlobal, Barcelona Institute for Global Health Hospital Clínic‐Universitat de Barcelona Barcelona Spain
                [2 ] IGTP Institut d'Investigació Germans Trias i Pujol Badalona (Barcelona) Spain
                [3 ] CIBERINFEC ISCIII‐CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III Madrid Spain
                [4 ] Departamento de Ciências Farmacêuticas Laboratório de Imunologia Celular e Bioquímica de Fungos e Protozoários Departamento de Ciências Farmacêuticas Instituto de Ciências Ambientais Químicas e Farmacêuticas Universidade Federal de São Paulo (UNIFESP) São Paulo Brazil
                [5 ] Department of Biomolecular Sciences Weizmann Institute of Science (WIS) Rehovot Israel
                [6 ] The Research Institute of the McGill University Health Centre McGill University Montréal Québec Canada
                [7 ] Department of Chemical Research Support WIS Rehovot Israel
                [8 ] Department of Immunotherapy and Leishmania Vaccine Research Pasteur Institute of Iran Tehran Iran
                [9 ] Flow Cytometry Unit Life Sciences Core Facilities, WIS Rehovot Israel
                [10 ] Instituto René Rachou/FIOCRUZ – MG Belo Horizonte Minas Gerais Brazil
                [11 ] Departamento de Análises Clínicas e Toxicológicas Faculdade de Farmácia, Universidade Federal de Minas Gerais (UFMG) Belo Horizonte Minas Gerais Brasil
                [12 ] Host‐Parasite Interactions Group Institute of Research and Innovation in Health University of Porto Porto Portugal
                [13 ] Department of Biological Sciences Faculty of Pharmacy University of Porto Porto Portugal
                [14 ] Faculty of Veterinary Medicine Université de Montréal Québec Canada
                [15 ] EVAHPI ‐ Extracellular Vesicles and Host‐Parasite Interactions Research Group Laboratório de Biologia Molecular e Sistemática de Tripanossomatideos Instituto Carlos Chagas‐Fiocruz Curitiba Paraná Brasil
                [16 ] Departament de Bioquímica i Biologia Molecular, Facultat de Ciències Biològiques Universitat de València Burjassot Valencia Spain
                [17 ] Àrea de Parasitologia, Departament de Farmàcia i Tecnologia Farmacèutica i Parasitologia Universitat de València Burjassot Valencia Spain
                [18 ] Laboratório de Biologia Molecular de Parasitas e Fungos, Centro de Parasitologia e Micologia Instituto Adolfo Lutz (IAL) São Paulo Brasil
                [19 ] Laboratório de Regulação da Expressão Gênica Instituto Carlos Chagas Fiocruz Paraná Curitiba Brazil
                [20 ] Research Center in Infectious Diseases Division of Infectious Disease and Immunity CHU de Quebec Research Center Department of Microbiology Infectious Disease and Immunology Faculty of Medicine University Laval Quebec City Quebec Canada
                [21 ] ICREA Institució Catalana de Recerca i Estudis Avanc¸ats (ICREA) Barcelona Spain
                [22 ] Department of Biological Sciences Border Biomedical Research Center The University of Texas at El Paso El Paso Texas USA
                [23 ] Departamento de Microbiologia Imunologia e Parasitologia, UNIFESP São Paulo Brazil
                Article
                10.1002/jex2.117
                0c5c7e0a-3374-48ce-b435-691cf3eb5fda
                © 2023

                http://creativecommons.org/licenses/by-nc-nd/4.0/

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