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      Engineered extracellular vesicle-based gene therapy for the treatment of discogenic back pain

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          Abstract

          Painful musculoskeletal disorders such as intervertebral disc (IVD) degeneration associated with chronic low back pain (termed “Discogenic back pain”, DBP), are a significant socio-economic burden worldwide and contribute to the growing opioid crisis. Yet there are very few if any successful interventions that can restore the tissue’s structure and function while also addressing the symptomatic pain. Here we have developed a novel non-viral gene therapy, using engineered extracellular vesicles (eEVs) to deliver the developmental transcription factor FOXF1 to the degenerated IVD in an in vivo model. Injured IVDs treated with eEVs loaded with FOXF1 demonstrated robust sex-specific reductions in pain behaviors compared to control groups. Furthermore, significant restoration of IVD structure and function in animals treated with FOXF1 eEVs were observed, with significant increases in disc height, tissue hydration, proteoglycan content, and mechanical properties. This is the first study to successfully restore tissue function while modulating pain behaviors in an animal model of DBP using eEV-based non-viral delivery of transcription factor genes. Such a strategy can be readily translated to other painful musculoskeletal disorders.

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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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            Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.

            Differentiated cells can be reprogrammed to an embryonic-like state by transfer of nuclear contents into oocytes or by fusion with embryonic stem (ES) cells. Little is known about factors that induce this reprogramming. Here, we demonstrate induction of pluripotent stem cells from mouse embryonic or adult fibroblasts by introducing four factors, Oct3/4, Sox2, c-Myc, and Klf4, under ES cell culture conditions. Unexpectedly, Nanog was dispensable. These cells, which we designated iPS (induced pluripotent stem) cells, exhibit the morphology and growth properties of ES cells and express ES cell marker genes. Subcutaneous transplantation of iPS cells into nude mice resulted in tumors containing a variety of tissues from all three germ layers. Following injection into blastocysts, iPS cells contributed to mouse embryonic development. These data demonstrate that pluripotent stem cells can be directly generated from fibroblast cultures by the addition of only a few defined factors.
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              RNA delivery by extracellular vesicles in mammalian cells and its applications

              The term ‘extracellular vesicles’ refers to a heterogeneous population of vesicular bodies of cellular origin that derive either from the endosomal compartment (exosomes) or as a result of shedding from the plasma membrane (microvesicles, oncosomes and apoptotic bodies). Extracellular vesicles carry a variety of cargo, including RNAs, proteins, lipids and DNA, which can be taken up by other cells, both in the direct vicinity of the source cell and at distant sites in the body via biofluids, and elicit a variety of phenotypic responses. Owing to their unique biology and roles in cell–cell communication, extracellular vesicles have attracted strong interest, which is further enhanced by their potential clinical utility. Because extracellular vesicles derive their cargo from the contents of the cells that produce them, they are attractive sources of biomarkers for a variety of diseases. Furthermore, studies demonstrating phenotypic effects of specific extracellular vesicle-associated cargo on target cells have stoked interest in extracellular vesicles as therapeutic vehicles. There is particularly strong evidence that the RNA cargo of extracellular vesicles can alter recipient cell gene expression and function. During the past decade, extracellular vesicles and their RNA cargo have become better defined, but many aspects of extracellular vesicle biology remain to be elucidated. These include selective cargo loading resulting in substantial differences between the composition of extracellular vesicles and source cells; heterogeneity in extracellular vesicle size and composition; and undefined mechanisms for the uptake of extracellular vesicles into recipient cells and the fates of their cargo. Further progress in unravelling the basic mechanisms of extracellular vesicle biogenesis, transport, and cargo delivery and function is needed for successful clinical implementation. This Review focuses on the current state of knowledge pertaining to packaging, transport and function of RNAs in extracellular vesicles and outlines the progress made thus far towards their clinical applications.
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                Author and article information

                Journal
                8100316
                1138
                Biomaterials
                Biomaterials
                Biomaterials
                0142-9612
                1878-5905
                29 May 2024
                July 2024
                01 April 2024
                01 July 2024
                : 308
                : 122562
                Affiliations
                [a ]Department of Biomedical Engineering, College of Engineering, The Ohio State University, USA
                [b ]Biophysics Graduate Program, The Ohio State University, USA
                [c ]Department of Mechanical Engineering, College of Engineering, The Ohio State University, USA
                [d ]Department of Biology, College of Arts and Sciences, The Ohio State University, USA
                [e ]Department of Orthopedics, The Ohio State University Wexner Medical Center, USA
                [f ]Small Animal Imaging Center Shared Resources, Wexner Medical Center, USA
                [g ]Department of Neuroscience, The Ohio State University, USA
                [h ]Institute for Behavioral Medicine Research, Neurological Institute, The Ohio State University, USA
                [i ]Leni and Peter W. May Department of Orthopaedics, Icahn School of Medicine at Mount Sinai, USA
                [j ]Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, The University of Manchester, Manchester, UK
                [k ]NIHR Manchester Musculoskeletal Biomedical Research Centre, Manchester University, NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK
                [l ]Department of Neurosurgery, The Ohio State University, USA
                [m ]Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, USA
                Author notes
                [* ]Corresponding author. The Ohio State University, 3016 Fontana Laboratories 140 W. 19th Ave., Columbus, OH, 43210, USA. Purmessurwalter.1@ 123456osu.edu (D. Purmessur)
                [** ]Corresponding author. The Ohio State University, 3002 Fontana Laboratories 140 W. 19th Ave., Columbus, OH, 43210, USA. Higuitacastro.1@ 123456osu.edu (N. Higuita-Castro)
                [1]

                Indicates equal contribution.

                Article
                NIHMS1994744
                10.1016/j.biomaterials.2024.122562
                11164054
                38583365
                444b89d7-1d1c-4231-91a9-c0490146c878

                This is an open access article under the CC BY-NC license ( http://creativecommons.org/licenses/by-nc/4.0/).

                History
                Categories
                Article

                Biomaterials & Organic materials
                engineered extracellular vesicles,cell reprogramming,low back pain,intervertebral disc,non-viral gene delivery,nanocarriers

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