June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Interleukin-18 induced retinal pigment eithelium cell death, but did not suppress choroidal neovascularization in mice
Author Affiliations & Notes
  • Ryo Ijima
    Ophthalmology, Nagoya Univ Grad School of Med, Nagoya, Japan
  • Hiroki Kaneko
    Ophthalmology, Nagoya Univ Grad School of Med, Nagoya, Japan
  • Shu Kachi
    Ophthalmology, Nagoya Univ Grad School of Med, Nagoya, Japan
  • Hiroko Terasaki
    Ophthalmology, Nagoya Univ Grad School of Med, Nagoya, Japan
  • Footnotes
    Commercial Relationships Ryo Ijima, None; Hiroki Kaneko, None; Shu Kachi, None; Hiroko Terasaki, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 321. doi:
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      Ryo Ijima, Hiroki Kaneko, Shu Kachi, Hiroko Terasaki; Interleukin-18 induced retinal pigment eithelium cell death, but did not suppress choroidal neovascularization in mice. Invest. Ophthalmol. Vis. Sci. 2013;54(15):321.

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

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Abstract

Purpose: To examine the biological effect of interleukin-18 (IL-18) on retinal pigment epithelium (RPE) cell viability and choroidal neovascularization (CNV) in mice.

Methods: Mouse recombinant (rIL-18) and neutralizing antibody for IL-18 were commercially purchased and resuspended with PBS. Subretinally mouse rIL-18 was injected. PBS injected eyes were used as control. Seven days after subretinal injection, fundus was checked and RPE was collected to examined cleaved caspase-3 expression in ELISA. Laser-induced choroidal neovascularizations (CNVs) were performed in the eyes of 6 week-old male C57Bl/6J mice, followed by intravitreous injection of 1ug rIL-18. The eyes injected with PBS after laser-CNVs were used as control. Neutralizing antibody for IL-18 (0.3ug) was also injected intravitreously after inducing laser-CNV. The eye injected with isotype control (0.3ug) was used as control. Seven days after laser and intravitreous injection, eyes were fixed with 4% paraformaldehyde, and stained with isolection B4. CNV volumes were analyzed using confocal microscope (Nikon).

Results: The caspase-3 expression in the RPE of the eye injected with rIL-18 showed significantly higher than those injected with PBS. However, CNV volume in the eyes injected with rIL-18 did not show significant difference compared with those injected with PBS. Furthermore, CNV volume in the eyes injected with IL-18 antibody did not show significant difference compared with those injected with isotype control.

Conclusions: These results indicated that IL-18 induced RPE cell death after subretinal injection, but did not show pro- or anti-angiogenic effects on laser-induced CNV in mice.

Keywords: 453 choroid: neovascularization • 701 retinal pigment epithelium  
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