September 2016
Volume 57, Issue 12
Open Access
ARVO Annual Meeting Abstract  |   September 2016
In vivo fluorescence retinal imaging following AAV2-mediated gene delivery in the rat retina
Author Affiliations & Notes
  • Joo Yong Lee
    Ophthalmology, Asan Medical Center, Seoul,
  • Heuiran Lee
    Department of Microbiology, Cellular Dysfunction Research Center, Asan Medical Center, Seoul, Korea (the Republic of)
  • Ji Hyun Kim
    Department of Microbiology, Cellular Dysfunction Research Center, Asan Medical Center, Seoul, Korea (the Republic of)
  • Footnotes
    Commercial Relationships   Joo Yong Lee, None; Heuiran Lee, None; Ji Hyun Kim, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science September 2016, Vol.57, 4036. doi:
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    • Get Citation

      Joo Yong Lee, Heuiran Lee, Ji Hyun Kim; In vivo fluorescence retinal imaging following AAV2-mediated gene delivery in the rat retina. Invest. Ophthalmol. Vis. Sci. 2016;57(12):4036.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To evaluate longitudinal gene expression patterns by retinal imaging using a modified custom-built confocal laser-scanning microscope in experimental rats after intravitreal injection of recombinant adeno-associated virus 2 (rAAV2-GFP).

Methods : Ten 9-week Wistar rats were divided into two groups: experimental group (group 1) that received a rAAV2-GFP intravitreal injection and control group (group 2) that received a vehicle. After anesthesia using a Zoletil intraperitoneal injection, 8 µL of rAAV2-GFP in group 1 or vehicle in group 2 was injected intravitreally using a 33-G Hamilton syringe. In vivo fluorescence retinal images were acquired under anesthesia at 2, 4, 6, and 13 days after rAAV or vehicle delivery.

Results : Differences in GFP fluorescence were identified starting from day 2 after the intravitreal injection of rAAV2-GFP in group 1. Between days 4 and 6, the intensity and area of fluorescence in the retina began to increase and peaked at day 13. Based on the pattern of GFP expression, the axon of the nerve fiber layer ganglion cell was identified. In group 2, eyes treated with the vehicle showed a small amount of autofluorescence in a limited area for up to 2 weeks, with no increase in intensity during this period.

Conclusions : In vivo retinal imaging confirmed gene expression within 2 weeks after the intravitreal injection of rAAV2-GFP. Gene transfer and expression in the rat retina occurs quickly and appears to peak within 2 weeks of gene delivery. In vivo retinal imaging may be a useful non-invasive tool to continuously monitor gene expression in the retina over time.

This is an abstract that was submitted for the 2016 ARVO Annual Meeting, held in Seattle, Wash., May 1-5, 2016.

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