March 1998
Volume 39, Issue 3
Free
Articles  |   March 1998
Protection of mouse photoreceptors by survival factors in retinal degenerations.
Author Affiliations
  • M M LaVail
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • D Yasumura
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • M T Matthes
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • C Lau-Villacorta
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • K Unoki
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • C H Sung
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
  • R H Steinberg
    Department of Anatomy, University of California, San Francisco 94143-0730, USA.
Investigative Ophthalmology & Visual Science March 1998, Vol.39, 592-602. doi:https://doi.org/
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      M M LaVail, D Yasumura, M T Matthes, C Lau-Villacorta, K Unoki, C H Sung, R H Steinberg; Protection of mouse photoreceptors by survival factors in retinal degenerations.. Invest. Ophthalmol. Vis. Sci. 1998;39(3):592-602. doi: https://doi.org/.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: To examine the protective effect of a number of survival factors on degenerating photoreceptors in mutant mice with naturally occurring inherited retinal degenerations, including retinal degeneration (rd/rd), retinal degeneration slow (rds/rds), nervous (nr/nr), and Purkinje cell degeneration (pcd/pcd), in three different forms of mutant rhodopsin transgenic mice and in light damage in albino mice. METHODS: Various survival factors were injected intravitreally into one eye of mice at or soon after the beginning of photoreceptor degeneration, with the opposite eye serving as the control, and the eyes were examined histologically at later ages. The survival factors included brain-derived neurotrophic factor (BDNF), neurotrophin-3, neurotrophin-4, ciliary neurotrophic factor (CNTF), Axokine (a mutein of CNTF), leukemia inhibitory factor, basic fibroblast growth factor, and nerve growth factor and insulin-like growth factor II, either alone or in various combinations. RESULTS: Photoreceptor degeneration was slowed in rd/rd and nr/nr mutant mice and in Q344ter mutant rhodopsin mice by certain forms of CNTF; the degeneration in Q344ter mice was slowed by Axokine and by leukemia inhibitory factor; and the degeneration in a few nr/nr mice was slowed by BDNF. The other agents were ineffective in these mice, and none of the agents were effective in the other mutants and other mutant rhodopsin transgenic mice. However, light damage experiments that compared agent effectiveness in albino mice versus rats suggested a significant delivery problem with the very small mouse eye, thereby making the interpretation of negative findings equivocal in mutant mice. Basic fibroblast growth factor failed to protect the mouse retina from the damaging effects of constant light, whereas it showed a strong protective effect in the rat, indicating an important species difference. CONCLUSIONS: The slowing of degeneration in the rd/rd and Q344ter mutant mice demonstrated that intraocularly injected survival factors can protect photoreceptors from degenerating in animal models with the same or similar genetic defects as those in human inherited retinal degenerations.

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