| First Author | Fischer MD | Year | 2010 |
| Journal | Invest Ophthalmol Vis Sci | Volume | 51 |
| Issue | 10 | Pages | 5254-9 |
| PubMed ID | 20445120 | Mgi Jnum | J:171407 |
| Mgi Id | MGI:4949836 | Doi | 10.1167/iovs.09-5139 |
| Citation | Fischer MD, et al. (2010) In vivo assessment of retinal vascular wall dimensions. Invest Ophthalmol Vis Sci 51(10):5254-9 |
| abstractText | PURPOSE: Retinal blood vessel diameter and arteriovenous ratio (AVR) are commonly used diagnostic parameters. Because vascular walls are typically not visible in funduscopy, clinical AVR estimation is based on the lumen rather than the entire vessel diameter. Here the authors used a transgenic mouse model to quantify AVR in vivo based on total vessel dimensions (wall and lumen). METHODS: Confocal scanning laser ophthalmoscopy (cSLO) and indocyanine green angiography of the retinal vasculature were performed in wild-type and transgenic mice expressing green fluorescent protein (GFP) under the transcriptional control of the smooth muscle type alpha-actin (alphaSMA) promoter. Spectral-domain-OCT and ERG were performed to control for integrity of retinal structure and function in vivo and histology to demonstrate the location of GFP expression. RESULTS: Native cSLO imaging and angiography yielded only inner vessel diameters similar to those observed through clinical funduscopy. In alphaSMA-GFP mice, autofluorescence imaging of the GFP-marked vascular walls also allowed the determination of outer vessel diameters. The mean AVR based on either inner diameter (AVR(id) = 0.72 +/- 0.08) or outer diameter (AVR(od) = 0.97 +/- 0.09) measurements were significantly different (P < 0.01). CONCLUSIONS: Transgenic alphaSMA-GFP expression in murine vessel wall components allowed quantification of retinal vessel outer diameters in vivo. Although arterioles and venules differ in lumen and vessel wall width, they share a common outer diameter, leading to an AVR(od) close to unity. Because vessel walls are primary targets in common hypertensive and metabolic diseases, alphaSMA-GFP transgenic mice may prove valuable in the detailed assessment of such disorders in vivo. |
