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Publication : Preservation of retinoid influx into eye tissues of ABCR-deficient mice.

First Author  Qtaishat NM Year  2007
Journal  Curr Eye Res Volume  32
Issue  12 Pages  1073-82
PubMed ID  18085472 Mgi Jnum  J:130834
Mgi Id  MGI:3772409 Doi  10.1080/02713680701715933
Citation  Qtaishat NM, et al. (2007) Preservation of retinoid influx into eye tissues of ABCR-deficient mice. Curr Eye Res 32(12):1073-82
abstractText  Using an in vivo radiolabeling technique, we investigated the movement of retinoid into the retinal pigment epithelium (RPE) of the abcr-/- mouse, which lacks the photoreceptor ABCR protein and is a model for Stargardt disease. Eye tissues and serum obtained from dark-adapted, 5- to 8-month-old abcr-/- and control mice following the intraperitoneal injection of all-trans ((3)H)retinol were analyzed to determine the inferred influx of retinoid from the serum into the RPE. At 4.5 hr post-injection, the inferred all-trans retinol influx in abcr-/- mice, which possess the leucine 450 variant of RPE65 protein, was 0.011 +/- 0.004 nmol (n = 3). This value did not differ significantly from that determined in age-matched controls possessing the methionine 450 variant of RPE65 (0.015 +/- 0.003 nmol; n = 3) or from 3-month-old wildtype mice that possess the leucine 450 RPE65 variant (0.020 +/- 0.007; n = 4). Thus, the absence of ABCR does not significantly compromise the passage of retinoid from the serum into the RPE under dark-adapted conditions.
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