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      Expanding applications of allogeneic platelets, platelet lysates, and platelet extracellular vesicles in cell therapy, regenerative medicine, and targeted drug delivery

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          Abstract

          Platelets are small anucleated blood cells primarily known for their vital hemostatic role. Allogeneic platelet concentrates (PCs) collected from healthy donors are an essential cellular product transfused by hospitals to control or prevent bleeding in patients affected by thrombocytopenia or platelet dysfunctions. Platelets fulfill additional essential functions in innate and adaptive immunity and inflammation, as well as in wound-healing and tissue-repair mechanisms. Platelets contain mitochondria, lysosomes, dense granules, and alpha-granules, which collectively are a remarkable reservoir of multiple trophic factors, enzymes, and signaling molecules. In addition, platelets are prone to release in the blood circulation a unique set of extracellular vesicles (p-EVs), which carry a rich biomolecular cargo influential in cell–cell communications. The exceptional functional roles played by platelets and p-EVs explain the recent interest in exploring the use of allogeneic PCs as source material to develop new biotherapies that could address needs in cell therapy, regenerative medicine, and targeted drug delivery. Pooled human platelet lysates (HPLs) can be produced from allogeneic PCs that have reached their expiration date and are no longer suitable for transfusion but remain valuable source materials for other applications. These HPLs can substitute for fetal bovine serum as a clinical grade xeno-free supplement of growth media used in the in vitro expansion of human cells for transplantation purposes. The use of expired allogeneic platelet concentrates has opened the way for small-pool or large-pool allogeneic HPLs and HPL-derived p-EVs as biotherapy for ocular surface disorders, wound care and, potentially, neurodegenerative diseases, osteoarthritis, and others. Additionally, allogeneic platelets are now seen as a readily available source of cells and EVs that can be exploited for targeted drug delivery vehicles. This article aims to offer an in-depth update on emerging translational applications of allogeneic platelet biotherapies while also highlighting their advantages and limitations as a clinical modality in regenerative medicine and cell therapies.

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          Microenvironmental regulation of tumor progression and metastasis.

          Cancers develop in complex tissue environments, which they depend on for sustained growth, invasion and metastasis. Unlike tumor cells, stromal cell types within the tumor microenvironment (TME) are genetically stable and thus represent an attractive therapeutic target with reduced risk of resistance and tumor recurrence. However, specifically disrupting the pro-tumorigenic TME is a challenging undertaking, as the TME has diverse capacities to induce both beneficial and adverse consequences for tumorigenesis. Furthermore, many studies have shown that the microenvironment is capable of normalizing tumor cells, suggesting that re-education of stromal cells, rather than targeted ablation per se, may be an effective strategy for treating cancer. Here we discuss the paradoxical roles of the TME during specific stages of cancer progression and metastasis, as well as recent therapeutic attempts to re-educate stromal cells within the TME to have anti-tumorigenic effects.
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            Biological properties of extracellular vesicles and their physiological functions

            In the past decade, extracellular vesicles (EVs) have been recognized as potent vehicles of intercellular communication, both in prokaryotes and eukaryotes. This is due to their capacity to transfer proteins, lipids and nucleic acids, thereby influencing various physiological and pathological functions of both recipient and parent cells. While intensive investigation has targeted the role of EVs in different pathological processes, for example, in cancer and autoimmune diseases, the EV-mediated maintenance of homeostasis and the regulation of physiological functions have remained less explored. Here, we provide a comprehensive overview of the current understanding of the physiological roles of EVs, which has been written by crowd-sourcing, drawing on the unique EV expertise of academia-based scientists, clinicians and industry based in 27 European countries, the United States and Australia. This review is intended to be of relevance to both researchers already working on EV biology and to newcomers who will encounter this universal cell biological system. Therefore, here we address the molecular contents and functions of EVs in various tissues and body fluids from cell systems to organs. We also review the physiological mechanisms of EVs in bacteria, lower eukaryotes and plants to highlight the functional uniformity of this emerging communication system.
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              Specificities of secretion and uptake of exosomes and other extracellular vesicles for cell-to-cell communication

              The ability of exosomes to transfer cargo from donor to acceptor cells, thereby triggering phenotypic changes in the latter, has generated substantial interest in the scientific community. However, the extent to which exosomes differ from other extracellular vesicles in terms of their biogenesis and functions remains ill-defined. Here, we discuss the current knowledge on the specificities of exosomes and other types of extracellular vesicles, and their roles as important agents of cell-to-cell communication.
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                Author and article information

                Contributors
                thburnouf@gmail.com
                Journal
                J Biomed Sci
                J Biomed Sci
                Journal of Biomedical Science
                BioMed Central (London )
                1021-7770
                1423-0127
                14 September 2023
                14 September 2023
                2023
                : 30
                : 79
                Affiliations
                [1 ]GRID grid.412896.0, ISNI 0000 0000 9337 0481, Graduate Institute of Biomedical Materials and Tissue Engineering, College of Biomedical Engineering, , Taipei Medical University, ; 250 Wu-Xing Street, Taipei, 11031 Taiwan
                [2 ]GRID grid.412896.0, ISNI 0000 0000 9337 0481, International Ph.D. Program in Biomedical Engineering, College of Biomedical Engineering, , Taipei Medical University, ; Taipei, Taiwan
                [3 ]GRID grid.412896.0, ISNI 0000 0000 9337 0481, International Ph.D. Program in Cell Therapy and Regenerative Medicine, College of Medicine, , Taipei Medical University, ; Taipei, Taiwan
                [4 ]GRID grid.25152.31, ISNI 0000 0001 2154 235X, Saskatoon Cancer Centre and College of Medicine, , University of Saskatchewan, ; Saskatchewan, Canada
                [5 ]GRID grid.260539.b, ISNI 0000 0001 2059 7017, Present Address: Institute of Clinical Medicine, , National Yang-Ming Chiao Tung University, ; Taipei, Taiwan
                Author information
                http://orcid.org/0000-0002-0507-9243
                http://orcid.org/0000-0002-6996-5332
                http://orcid.org/0000-0003-0848-3206
                http://orcid.org/0000-0002-1593-4573
                http://orcid.org/0000-0001-9446-4030
                http://orcid.org/0000-0003-1201-7275
                Article
                972
                10.1186/s12929-023-00972-w
                10500824
                37704991
                e6b88d6b-eb4b-4243-acdb-12ca85a2fb65
                © National Science Council of the Republic of China (Taiwan) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 6 March 2023
                : 23 August 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004737, National Health Research Institutes;
                Award ID: NHRI-EX111-10920E
                Award ID: NHRI-EX110-10920EI
                Award ID: NHRI-EX109-10920EI
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004663, Ministry of Science and Technology, Taiwan;
                Award ID: 111-2314-B-038-025
                Award ID: 112-2923-E-038-001
                Award Recipient :
                Categories
                Review
                Custom metadata
                © National Science Council of the Republic of China (Taiwan) 2023

                Molecular medicine
                platelet,allogeneic platelet concentrate,human platelet lysate,extracellular vesicles,regenerative medicine,cell therapy

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