7-Ketocholesterol Induces Inflammation and Angiogenesis In Vivo: A Novel Rat Model

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Abstract

Accumulation of 7-Ketocholesterol (7KCh) in lipid deposits has been implicated in a variety of chronic diseases including atherosclerosis, Alzheimer's disease and age-related macular degeneration. 7KCh is known to be pro-inflammatory and cytotoxic to various types of cultured cells but little is known about its effects in vivo. In this study we have investigated the effects of 7KCh in vivo by implanting biodegradable wafers into the anterior chamber of the rat eye. The wafers were prepared using a mixture of two biodegradable polymers with different amounts of 7KCh. The 7KCh-containing implants induced massive angiogenesis and inflammation. By contrast, no angiogenesis and very little inflammation were observed with cholesterol-containing implants. The neovessel growth was monitored by fluorescein angiography. Neovessels were observed 4 days post implantation and peaked between 7 to 10 days. The angiography and isolectin IB4 labeling demonstrated that the neovessels originated from the limbus and grew through the cornea. Immunolabeling with anti-CD68 suggested that the 7KCh-containing implants had extensive macrophage infiltration as well as other cell types. A significant increase in VEGF was also observed in 7KCh-containing implants by fluorescent immunolabeling and by immunoblot of the aqueous humor (AH). Direct measurement of VEGF, IL-1β and GRO/KC demonstrated a marked elevation of these factors in the AH of the 7KCh-implants. In summary this study demonstrates two important things: 1) 7KCh is pro-angiogenic and pro-inflammatory in vivo and 2) implants containing 7KCh may be used to create a novel angiogenesis model in rats.

Figures

  • Figure 1. Wafer implantation into the rat anterior chamber. A. A full thickness corneal incision was made parallel to the plane of the iris (arrows). Wafers were introduced to the anterior chamber using toothless forceps (dotted circle), and displaced to its temporal position (dotted arrow) in the anterior chamber. B. Side-view schematic showing the approximate location of the implant. C. The final position of all implants was an average of 0.8 mm from the limbus (dotted line). Ch = cholesterol, 7KCh = 7-ketocholesterol, n = number of wafers implants. doi:10.1371/journal.pone.0056099.g001
  • Figure 2. Angiogenesis in Ch versus 7KCh implants. Ch (20% w/w) and 7KCh (10% w/w) implants were placed in the anterior chamber of the rat eye as described in Fig. 1. Both implants were imaged 7 days post implantation with and without fluorescein angiography. Arrows mark the locations of the iris, limbus and implants. doi:10.1371/journal.pone.0056099.g002
  • Figure 3. Effects of time and 7KCh concentrations on angiogenesis. Wafers containing 5, 7, 10 and 15% 7KCh (w/w) were implanted into rats anterior chambers as described in Fig. 1 and representative images are shown at 7, 10, 14 and 21 days. The vessel volume for each panel is shown in Fig. 4b, in mm2. doi:10.1371/journal.pone.0056099.g003
  • Figure 4. Technique used to quantify neovessel formation.
  • Figure 5. Localization of corneal neovessels with isolectin IB4. Cryosections of temporal corneas were prepared 14 days after implantation with a 20% 7KCh wafer. The sections were labeled with AlexaFluor 568 Isolectin IB4 (red) and the nuclei stained with DAPI (blue). A. DAPI stained section demonstrating the location of the corneal stroma and epithelium. B. Isolectin IB4 labeling of neovessels, corneal epithelium and iris. C. Combined image. Arrows mark the different structures. doi:10.1371/journal.pone.0056099.g005
  • Figure 6. Histological comparison of Ch and 7KCh implants using isolectin IB4. Rat eyes were implanted with 20% Ch and 7KCh wafers and cryosections prepared 14 days post implantation. A. Ch implant labeled with isolectin IB4. B. Ch implant dual labeled with DAPI. C. 7KCh implant labeled with isolectin IB4. D. 7KCh implant dual labeled with DAPI. doi:10.1371/journal.pone.0056099.g006
  • Figure 7. Localization of CD68 positive cells and VEGF in Ch and 7KCh implants. Rat eyes were implanted with 20% Ch and 7KCh wafers and cryosections prepared 14 days post implantation. The sections were labeled with AlexaFluor 488 (green) for anti-CD68 or antiVEGF and the nuclei stained with DAPI (blue). A. Ch implant, anti-CD68. B. 7KCh implant, anti-CD68. C. Ch implant, anti-VEGF. D. 7KCh implant, anti-VEGF. doi:10.1371/journal.pone.0056099.g007
  • Table 1. Protein concentration of aqueous humor.

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CITATION STYLE

APA

Amaral, J., Lee, J. W., Chou, J., Campos, M. M., & Rodríguez, I. R. (2013). 7-Ketocholesterol Induces Inflammation and Angiogenesis In Vivo: A Novel Rat Model. PLoS ONE, 8(2). https://doi.org/10.1371/journal.pone.0056099

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