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J. Lipid Res.
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Journal of Lipid Research, Vol. 43, 590-597, April 2002
Copyright © 2002 by Lipid Research, Inc.

Targeted disruption of the mouse cis-retinol dehydrogenase gene: visual and nonvisual functions

Enyuan Shanga, Katherine Laib, Alan I. Packerc, Jisun Paikb, William S. Blanera,b, Milena de Morais Vieirab, Peter Gourasd, and Debra J. Wolgemutha,c,e,f,g
a The Institute of Human Nutrition, Columbia University College of Physicians and Surgeons, New York, NY 10032
b Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY 10032
c Department of Genetics and Development, Columbia University College of Physicians and Surgeons, New York, NY 10032
d Department of Ophthalmology, Columbia University College of Physicians and Surgeons, New York, NY 10032
e Center for Reproductive Sciences, Columbia University College of Physicians and Surgeons, New York, NY 10032
f Department of Obstetrics and Gynecology, Columbia University College of Physicians and Surgeons, New York, NY 10032
g Herbert Irving Comprehensive Cancer Center, Columbia University College of Physicians and Surgeons, New York, NY 10032

Correspondence to: William S. Blaner, at the Department of Medicine, Columbia University College of Physicians and Surgeons, Hammer Building, Room 502, 701 West 168th Street, New York, NY 10032.

It has been proposed that cis-retinol dehydrogenase (cRDH) acts within the body to catalyze the oxidation of 9-cis-retinol, an oxidative step needed for 9-cis-retinoic acid synthesis, the oxidation of 11-cis-retinol [an oxidative step needed for 11-cis-retinal (visual chromophore) synthesis], and 3{alpha}-hydroxysteroid transformations. To assess in vivo the physiological importance of each of these proposed actions of cRDH, we generated cRDH-deficient (cRDH-/-) mice. The cRDH-/- mice reproduce normally and appear to be normal. However, the mutant mice do have a mild visual phenotype of impaired dark adaptation. This phenotype is evidenced by electroretinagram analysis of the mice and by biochemical measures of eye levels of retinoid intermediates during recovery from an intense photobleach. Although it is thought that cRDH is expressed in the eye almost solely in retinal pigment epithelial cells, we detected cRDH expression in other retinal cells, including ganglion cells, amacrine cells, horizontal cells, and the inner segments of the rod photoreceptor cells. Aside from the eye, there are no marked differences in retinoid levels in other tissues throughout the body for cRDH-/- compared with cRDH+/+ mice. Moreover, we did not detect any non-visual phenotypic changes for cRDH-/- mice, suggesting that these mice do not have problems in metabolizing 3{alpha}-hydroxysteroids.

Thus, cRDH may act essentially in the visual cycle but is redundant for catalyzing 9-cis-retinoic acid formation and 3{alpha}-hydroxysteroid metabolism.—Shang, E., K. Lai, A. I. Packer, J. Paik, W. S. Blaner, M. de Morais Vieira, P. Gouras, and D. J. Wolgemuth. Targeted disruption of the mouse cis-retinol dehydrogenase gene: visual and nonvisual functions. J. Lipid Res. 2002. 43: 590–597.

Supplementary key words: vitamin A, retinoid, vision, knockout mice, 11-cis-retinol, steroid, retinol, eye


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