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dc.rights.licenseCC-BY-NC-ND
dc.contributor.advisorCaiazzo, Massimiliano
dc.contributor.authorBreejen, Anne den
dc.date.accessioned2025-07-31T00:01:18Z
dc.date.available2025-07-31T00:01:18Z
dc.date.issued2025
dc.identifier.urihttps://studenttheses.uu.nl/handle/20.500.12932/49438
dc.description.abstractCellular reprogramming is the conversion of a cell into another cell type by the forced expression of cell-lineage transcription factors. One example of cellular reprogramming is direct neuronal reprogramming, in which neurons or other neuronal cells are directly converted from fibroblasts or astrocytes. These induced neurons have significant potential for research and therapeutic applications, such as in cell replacement therapy. However, current delivery strategies of conversion factors have fundamental limitations. In this review, we outlined the current used delivery technologies in neuronal reprogramming and their limitations and advantages. The first employed delivery strategies were mainly viral systems, such as lentiviruses or adeno-associated viruses, yet these systems cause major safety concerns, including risk for insertional mutagenesis and inflammation. Several non-viral delivery systems, among which are physical and chemical methods, have been investigated as well. However, these systems exert inferior reprogramming efficiency. Emerging delivery technologies, such as lipid-based nanoparticles or particles derived by combinations of delivery materials, could provide new opportunities in safe and effective delivery for neuronal reprogramming. Employing target specific and efficient engineered delivery systems is essential to proceed neuronal reprogramming into clinical practice.
dc.description.sponsorshipUtrecht University
dc.language.isoEN
dc.subjectNeuronal reprogramming has potential for replacement or generation of neurons for clinical applications in neurodegenerative disorders and brain injury. However, the current-used technologies for the delivery of molecular determinants in neuronal reprogramming hamper the proceeding into clinical practice. In this review, I describe the current advancements and challenges of these delivery mechanisms and a prospective on future delivery technologies for clinical translation.
dc.titleOverview of Delivery Technologies for Molecular Determinants in Neuronal Reprogramming
dc.type.contentMaster Thesis
dc.rights.accessrightsOpen Access
dc.subject.courseuuDrug Innovation
dc.thesis.id42854


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