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Nanotechnologically reprogrammed cellular medicines
16th national competition for scientific and technical research
Gene and regenerative therapy
Research Centre or Institution : Centro Singular en Medicina Molecular y Enfermedades Crónicas. Universidad de Santiago de Compostela
Abstract
The use of stem cells as therapeutic tools is associated with the regeneration of complex tissues and organs. However, these applications are currently restricted in clinical terms due to the lack of availability of stem cells, together with the difficulty of inducing conversion to target lines safely and efficiently. This proposal involves a cellular medicine platform based on priming lines with the potential characteristics of efficacy, safety and logistic convenience, turning them into tools for clinical use. The technology presented is based on the concept of directly reprogramming target cell lines, without going through a previous state of pluripotency ("line priming"). To achieve these aims, line priming will take place using a population of cells that are accessible and available in sufficient amounts, using synthetic nanovectors with a high level of biosafety. Finally, the primed cells will be integrated within biomimetic scaffolding able to direct the association of cells for the formation of structural tissues. This project is intended to achieve an initial proof of concept by priming functional human chondrocytes and neurons and then studying the possibility of assembling these cells for the formation of hyaline cartilage and layers of interconnected neurons.
During these first months of the project, work is being undertaken to optimise gene transfer methodology for line priming. More specifically, work is taking place on optimising the gene sequences using several synthetic and biosynthetic methods to promote the maximum expression of the transgenes introduced. Using these methods, up to 70% of adult stem cells express the transgene. This work will be complemented by another nanotechnological approach: the design of high transfectability synthetic nanovectors. Additionally, during these first months, a genetic sequence is being designed that is able to prime chondrogenic lines based on adult stem cells.
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23
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Panel Discussion Nanomedicina: liberación de fármacos con terapia focalizada, diagnosis y nanodispositivos Madrid, Monday, 23 January 2023, 17:00 hours
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6
Feb
2024
Conference NANOMEDICINA: del laboratorio a la clínica Madrid, Martes, 06 de febrero de 2024, 19:00 horas
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9
May
2024
Conference Genes de mosca y genes humanos: una comparación Madrid, Jueves 09 de mayo de 2024, 19:00 horas
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- Extracellular vesicles biomarkers for the diagnosis and prognosis of post-surgical septic shock 2018 Senior Researcher : Eduardo Tamayo Gómez Research Centre or Institution : Hospital Clínico Universitario de Valladolid
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Eric D. Green: “La genómica debe integrarse en la medicina convencional”
Published on 03/12/2021
Stem cells and organoids. Unlocking their potential to understand and treat disease
Febrero 2018 Nature PapersEnd of main content