20 research outputs found

    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

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    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

    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

    Get PDF
    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

    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

    Get PDF

    Protective effect of the naturally occurring, biologically active compound S-methylmethionine in maize seedlings exposed to a short period of cold

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    The work was aimed at investigating short-term metabolic changes caused by S-methylmethionine (SMM) and at clarifying the gene expression background of these changes in order to gain a better understanding of the protective effect of SMM against stress. When examining the expression of genes coding for the enzymes responsible for the biosynthesis of polyamines, which play an important role in responses to low temperature stress, and that of the C-repeat binding transcription factor (CBF1) gene, it was found that both SMM and cold treatment increased the expression of genes responsible for the polyamine synthesis pathway starting from arginine. It caused only a slight increase when applied alone, but when SMM pre-treatment was followed by cold stress, it resulted in a considerable extent of up-regulation. SMM caused a similar increase in the expression of CBF1. The changes in the expression of genes responsible for the polyamine synthesis were clearly reflected in changes in the putrescine and agmatine contents, while the greater increase in the spermidine content was indicative of the role of SMM as a direct precursor in spermidine biosynthesis. The results demonstrated that, in addition to its direct effect on the sulphur metabolism and on polyamine biosynthesis, the protective effect of exogenous SMM was chiefly manifested in its influence on the expression of genes responsible for the biosynthesis of the polyamines important for stress responses and on the CBF1 transcription factor gene that acts as a regulator in cold stress
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