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      Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies

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          Summary

          Authors review the major factors that hinder successful cell engraftment and the strategies that have been studied to enhance the beneficial effects of cell therapy for regenerative medicine. It also provides a perspective on whether mesenchymal stromal cell-derived extracellular vesicle delivery, as a cell-free regenerative approach, may circumvent current cell therapy limitations.

          Abstract

          Cell-based therapies have the potential to revolutionize current treatments for diseases with high prevalence and related economic and social burden. Unfortunately, clinical trials have made only modest improvements in restoring normal function to degenerating tissues. This limitation is due, at least in part, to the death of transplanted cells within a few hours after transplant due to a combination of mechanical, cellular, and host factors. In particular, mechanical stress during implantation, extracellular matrix loss upon delivery, nutrient and oxygen deprivation at the recipient site, and host inflammatory response are detrimental factors limiting long-term transplanted cell survival. The beneficial effect of cell therapy for regenerative medicine ultimately depends on the number of administered cells reaching the target tissue, their viability, and their promotion of tissue regeneration. Therefore, strategies aiming at improving viable cell engraftment are crucial for regenerative medicine. Here we review the major factors that hamper successful cell engraftment and the strategies that have been studied to enhance the beneficial effects of cell therapy. Moreover, we provide a perspective on whether mesenchymal stromal cell-derived extracellular vesicle delivery, as a cell-free regenerative approach, may circumvent current cell therapy limitations.

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          Most cited references123

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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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            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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              Paracrine mechanisms of mesenchymal stem cell-based therapy: current status and perspectives.

              Mesenchymal stem cells (MSCs) are one of a few stem cell types to be applied in clinical practice as therapeutic agents for immunomodulation and ischemic tissue repair. In addition to their multipotent differentiation potential, a strong paracrine capacity has been proposed as the principal mechanism that contributes to tissue repair. Apart from cytokine/chemokine secretion, MSCs also display a strong capacity for mitochondrial transfer and microvesicle (exosomes) secretion in response to injury with subsequent promotion of tissue regeneration. These unique properties of MSCs make them an invaluable cell type to repair damaged tissues/organs. Although MSCs offer great promise in the treatment of degenerative diseases and inflammatory disorders, there are still many challenges to overcome prior to their widespread clinical application. Particularly, their in-depth paracrine mechanisms remain a matter for debate and exploration. This review will highlight the discovery of the paracrine mechanism of MSCs, regulation of the paracrine biology of MSCs, important paracrine factors of MSCs in modulation of tissue repair, exosome and mitochondrial transfer for tissue repair, and the future perspective for MSC-based therapy.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                02 October 2017
                October 2017
                : 18
                : 10
                : 2087
                Affiliations
                [1 ]Department of Research, Advanced Diagnostic, and Technological Innovation, Regina Elena National Cancer Institute, via E. Chianesi 53, Rome 00144, Italy; silvia.baldari@ 123456ifo.gov.it (S.B.); giuliana.dirocco@ 123456ifo.gov.it (G.D.R.)
                [2 ]Stem Cells and Regenerative Medicine Laboratory, Foundation Institute of Pediatric Research “Città della Speranza”, corso Stati Uniti 4, Padova 35127, Italy; m.piccoli@ 123456irpcds.org
                [3 ]Department of Women’s and Children’s Health, University of Padova, Via Giustiniani 3, Padova 35128, Italy; m.pozzobon@ 123456irpcds.org (M.P.); muraca@ 123456unipd.it (M.M.)
                Author notes
                [* ]Correspondence: gabriele.toietta@ 123456ifo.gov.it ; Tel.: +39-06-5266-2604
                Author information
                https://orcid.org/0000-0001-6211-0051
                https://orcid.org/0000-0001-9213-402X
                https://orcid.org/0000-0003-4182-2468
                Article
                ijms-18-02087
                10.3390/ijms18102087
                5666769
                28974046
                13c81f5b-0ac6-44f3-8af2-01cdf68aad7e
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 31 August 2017
                : 28 September 2017
                Categories
                Review

                Transplantation,Surgery,Cell biology,Molecular biology,Human biology,Life sciences
                cell therapy,anoikis,cell survival,stem cells,regenerative medicine,extracellular vesicles,cell transplantation,hypoxia,mesenchymal stromal cells

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