In Vivo Laser-Mediated Retinal Ganglion Cell Optoporation Using KV1.1 Conjugated Gold Nanoparticles.
Ariel M WilsonJavier MazzaferriÉric BergeronSergiy PatskovskyPaule Marcoux-ValiquetteSantiago CostantinoPrzemyslaw SapiehaMichel MeunierPublished in: Nano letters (2018)
Vision loss caused by retinal diseases affects hundreds of millions of individuals worldwide. The retina is a delicate central nervous system tissue stratified into layers of cells with distinct roles. Currently, there is a void in treatments that selectively target diseased retinal cells, and current therapeutic paradigms present complications associated with off-target effects. Herein, as a proof of concept, we introduce an in vivo method using a femtosecond laser to locally optoporate retinal ganglion cells (RGCs) targeted with functionalized gold nanoparticles (AuNPs). We provide evidence that AuNPs functionalized with an antibody toward the cell-surface voltage-gated K+ channel subunit KV1.1 can selectively deliver fluorescently tagged siRNAs or fluorescein isothiocyanate-dextran dye into retinal cells when irradiated with an 800 nm 100 fs laser. Importantly, neither AuNP administration nor irradiation resulted in RGC death. This system provides a novel, non-viral-based approach that has the potential to selectively target retinal cells in diseased regions while sparing healthy areas and may be harnessed in future cell-specific therapies for retinal degenerative diseases.
Keyphrases
- induced apoptosis
- gold nanoparticles
- cell cycle arrest
- diabetic retinopathy
- optical coherence tomography
- endoplasmic reticulum stress
- magnetic resonance imaging
- optic nerve
- stem cells
- quantum dots
- cell death
- single cell
- radiation therapy
- cell surface
- cell proliferation
- climate change
- risk factors
- mesenchymal stem cells
- risk assessment
- image quality
- bone marrow
- human health
- current status
- pi k akt
- contrast enhanced
- tandem mass spectrometry