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PMID: 9237863 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Variability in rate of cone degeneration in the retinal degeneration (rd/rd) mouse.

Experimental eye research ·Vol. 65 ·No. 1 ·1997-07-00 ·Pages 45-50

LaVail MM, Matthes MT, Yasumura D, Steinberg RH

Abstract

The retinas of rd/rd mice with inherited retinal degeneration were examined histologically at postnatal days 60-66, an age when most rod cells already have degenerated and disappeared but when a significant number of cones are still present. We observed an unexpected hemispheric asymmetry and large variability in the number of surviving cones. Significantly more cones survived in the inferior than in the superior hemisphere in most retinas, although in about 15% of animals the hemispheric asymmetry was absent or was reversed. The number of surviving cones was highly variable from animal to animal, ranging from 3-30, a factor of 10, within the superior hemisphere, and from 7-51, a factor greater than 7, in the inferior hemisphere. If the specific hemisphere was ignored, the number ranged from 3-51, a factor of 17. These findings have significance for the examination of cone survival in the late stages of degeneration in this widely studied mutant, including therapeutic studies using transplantation, gene therapy or survival factors, as well as for the identification of surviving cells using cone-specific markers.

MeSH Terms
Animals Mice Mice, Mutant Strains Retinal Cone Photoreceptor Cells/pathology Retinal Degeneration/pathology
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
LaVail M M
Department of Anatomy, University of California, San Francisco, CA, 94143-0730, USA.
Matthes M T
Yasumura D
Steinberg R H
Article Info
Journal
Experimental eye research
Abbr.
Exp Eye Res
ISSN
0014-4835
Published
1997-07-00
Pages
45-50
Language
English
Region
England
NLM ID
0370707
Subset
IM
Grants
NEI NIH HHS · EY01429 · United States
NEI NIH HHS · EY01919 · United States
NEI NIH HHS · EY06842 · United States
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