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A Thy1-CFP DBA/2J mouse line with cyan fluorescent protein expression in retinal ganglion cells

Published online by Cambridge University Press:  23 November 2009

IONA D. RAYMOND ,
ANGELA L. POOL ,
ALEJANDRO VILA  and
NICHOLAS C. BRECHA
IONA D. RAYMOND*
Affiliation:
Departments of Neurobiology & Medicine, David Geffen UCLA School of Medicine, Los Angeles, California
ANGELA L. POOL
Affiliation:
Departments of Neurobiology & Medicine, David Geffen UCLA School of Medicine, Los Angeles, California
ALEJANDRO VILA
Affiliation:
Department of Neurobiology and Anatomy, University of Texas Medical School at Houston, Houston, Texas
NICHOLAS C. BRECHA
Affiliation:
Departments of Neurobiology & Medicine, David Geffen UCLA School of Medicine, Los Angeles, California CURE, Division of Digestive Diseases, David Geffen UCLA School of Medicine, Los Angeles, California Jules Stein Eye Institute, David Geffen UCLA School of Medicine, Los Angeles, California VAGLAHS, Los Angeles, California
*
*Address correspondence and reprint requests to: Iona D. Raymond, Department of Neurobiology, David Geffen School of Medicine at UCLA, 10833 Le Conte Avenue, Box 951763, Los Angeles, CA 90095-1763. E-mail: [email protected]
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Abstract

A DBA/2J (D2) transgenic mouse line with cyan fluorescent protein (CFP) reporter expression in ganglion cells was developed for the analysis of ganglion cells during progressive glaucoma. The Thy1-CFP D2 (CFP-D2) line was created by congenically breeding the D2 line, which develops pigmentary glaucoma, and the Thy1-CFP line, which expresses CFP in ganglion cells. Microsatellite marker analysis of CFP-D2 progeny verified the genetic inclusion of the D2 isa and ipd loci. Specific mutations within these loci lead to dysfunctional melanosomal proteins and glaucomatous phenotype in D2 mice. Polymerase chain reaction analysis confirmed the inclusion of the Thy1-CFP transgene. CFP-fluorescent ganglion cells, 6–20 μm in diameter, were distributed in all retinal regions, CFP processes were throughout the inner plexiform layer, and CFP-fluorescent axons were in the fiber layer and optic nerve head. Immunohistochemistry with antibodies to ganglion cell markers NF-L, NeuN, Brn3a, and SMI32 was used to confirm CFP expression in ganglion cells. Immunohistochemistry with antibodies to amacrine cell markers HPC-1 and ChAT was used to confirm weak CFP expression in cholinergic amacrine cells. CFP-D2 mice developed a glaucomatous phenotype, including iris disease, ganglion cell loss, attrition of the fiber layer, and elevated intraocular pressure. A CFP-D2 transgenic line with CFP-expressing ganglion cells was developed, which has (1) a predominantly D2 genetic background, (2) CFP-expressing ganglion cells, and (3) age-related progressive glaucoma. This line will be of value for experimental studies investigating ganglion cells and their axons in vivo and in vitro during the progressive development of glaucoma.

Keywords

GlaucomaDBA/2JGanglion cellsFluorescent proteinTransgenic mouse
Type
Research Articles
Information
Visual Neuroscience , Volume 26 , Issue 5-6 , November 2009 , pp. 453 - 465
Copyright
Copyright © Cambridge University Press 2009

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