Nano-enhanced Optical Gene Delivery to Retinal Degenerated Mice
Autor: | Weldon Wright, Sulagna Bhattacharya, Samarendra K. Mohanty, Subrata Batabyal, Sivakumar Gajjeraman |
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Rok vydání: | 2019 |
Předmět: |
Retinal degeneration
Opsin genetic structures 02 engineering and technology Nod Biology Gene delivery Retina Macular Degeneration Mice 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Drug Discovery Genetics medicine Animals Humans Molecular Biology Genetics (clinical) 030304 developmental biology 0303 health sciences Electroporation Retinal Degeneration Gene Transfer Techniques Retinal Genetic Therapy Transfection Macular degeneration 021001 nanoscience & nanotechnology medicine.disease eye diseases Cell biology Disease Models Animal HEK293 Cells medicine.anatomical_structure chemistry 030221 ophthalmology & optometry Nanoparticles Molecular Medicine sense organs Visual Fields 0210 nano-technology |
Zdroj: | Current Gene Therapy. 19:318-329 |
ISSN: | 1566-5232 |
Popis: | Background: The efficient and targeted delivery of genes and other impermeable therapeutic molecules into retinal cells is of immense importance for the therapy of various visual disorders. Traditional methods for gene delivery require viral transfection, or chemical methods that suffer from one or many drawbacks, such as low efficiency, lack of spatially targeted delivery, and can generally have deleterious effects, such as unexpected inflammatory responses and immunological reactions. Methods: We aim to develop a continuous wave near-infrared laser-based Nano-enhanced Optical Delivery (NOD) method for spatially controlled delivery of ambient-light-activatable Muti-Characteristic opsin-encoding genes into retina in-vivo and ex-vivo. In this method, the optical field enhancement by gold nanorods is utilized to transiently permeabilize cell membrane, enabling delivery of exogenous impermeable molecules to nanorod-binding cells in laser-irradiated regions. Results and Discussion: With viral or other non-viral (e.g. electroporation, lipofection) methods, gene is delivered everywhere, causing uncontrolled expression over the whole retina. This will cause complications in the functioning of non-degenerated areas of the retina. In the NOD method, the contrast in temperature rise in laser-irradiated nanorod-attached cells at nano-hotspots is significant enough to allow site-specific delivery of large genes. The in-vitro and in-vivo results using NOD, clearly demonstrate in-vivo gene delivery and functional cellular expression in targeted retinal regions without compromising the structural integrity of the eye or causing immune response. Conclusion: The successful delivery and expression of MCO in the targeted retina after in-vivo NOD in the mice models of retinal degeneration opens a new vista for re-photosensitizing retina with geographic atrophies, such as in dry age-related macular degeneration. |
Databáze: | OpenAIRE |
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