|
|
||||||||
Investigative Ophthalmology & Visual Science, Vol 38, 2545-2553, Copyright © 1997 by Association for Research in Vision and Ophthalmology
ARTICLES AND REPORTS |
LA Levin, CL Schlamp, RL Spieldoch, KM Geszvain and RW Nickells
Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison 53792, USA. Llevin@macc.wisc.edu
PURPOSE: Retinal ganglion cells die by apoptosis after axotomy, and this process may reflect altered expression of cell-death genes. Several of these genes, including bcl-2, bcl-x, and bax, share homology at the amino acid level in the BH1 and BH2 domains, through which they also interact. To understand their role in the neuronal response to axotomy, the authors studied their expression in the adult rat retina and after optic nerve crush. METHODS: An initial survey was conducted with reverse transcription-polymerase chain reaction (RT-PCR), using oligonucleotides against identified members of this family and against the conserved BH1 and BH2 domains. Retinal bcl-xl expression at the messenger RNA (mRNA) and protein level was studied by RT-PCR, Northern blotting, RNase protection analysis, in situ hybridization, Western blotting, and immunofluorescence staining. The effect of retinal ganglion cell axotomy on the steady-state level of bcl-x mRNA was investigated. RESULTS: RT-PCR results indicated that rat retinal cells predominantly express the long form of bcl-x. Both clonal analysis and quantitative measurements using RNase protection assays demonstrated that bcl-xL message was at least 16 times more abundant than that of bcl-2. In situ hybridization and indirect immunofluorescence demonstrated that nearly all neuronal cells of the retina express bcl- x. Northern and RNase protection analyses showed a moderate decrease in bcl-xL message shortly after optic nerve crush. CONCLUSIONS: These findings suggest that the antideath gene bcl-xL is the predominant member of the bcl-2 family in the adult retina, and that its level decreases after optic nerve crush. Changes in bcl-xL expression may correlate with increased retinal ganglion cell apoptosis after axotomy.
This article has been cited by other articles:
![]() |
T Oshitari, S Yamamoto, N Hata, and S Roy Mitochondria- and caspase-dependent cell death pathway involved in neuronal degeneration in diabetic retinopathy Br. J. Ophthalmol., April 1, 2008; 92(4): 552 - 556. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. de Gooyer, K. A. Stevenson, P. Humphries, D. A. C. Simpson, T. A. Gardiner, and A. W. Stitt Retinopathy Is Reduced during Experimental Diabetes in a Mouse Model of Outer Retinal Degeneration Invest. Ophthalmol. Vis. Sci., December 1, 2006; 47(12): 5561 - 5568. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Zheng, R. E. Anderson, M.-P. Agbaga, E. B. Rucker III, and Y.-Z. Le Loss of BCL-XL in Rod Photoreceptors: Increased Susceptibility to Bright Light Stress Invest. Ophthalmol. Vis. Sci., December 1, 2006; 47(12): 5583 - 5589. [Abstract] [Full Text] [PDF] |
||||
![]() |
P Georges, E E Cornish, J M Provis, and M C Madigan Muller cell expression of glutamate cycle related proteins and anti-apoptotic proteins in early human retinal development Br. J. Ophthalmol., February 1, 2006; 90(2): 223 - 228. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. I. Swanson, C. R. Schlieve, C. J. Lieven, and L. A. Levin Neuroprotective Effect of Sulfhydryl Reduction in a Rat Optic Nerve Crush Model Invest. Ophthalmol. Vis. Sci., October 1, 2005; 46(10): 3737 - 3741. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. L. Schlamp, A. T. Thliveris, Y. Li, L. P. Kohl, C. Knop, J. A. Dietz, I. V. Larsen, P. Imesch, L. H. Pinto, and R. W. Nickells Insertion of the {beta}Geo Promoter Trap into the Fem1c Gene of ROSA3 Mice Mol. Cell. Biol., May 1, 2004; 24(9): 3794 - 3803. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Vrabec, C. J. Lieven, and L. A. Levin Cell-Type-Specific Opening of the Retinal Ganglion Cell Mitochondrial Permeability Transition Pore Invest. Ophthalmol. Vis. Sci., June 1, 2003; 44(6): 2774 - 2782. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Oshitari, M. Dezawa, S. Okada, M. Takano, H. Negishi, H. Horie, H. Sawada, T. Tokuhisa, and E. Adachi-Usami The Role of c-fos in Cell Death and Regeneration of Retinal Ganglion Cells Invest. Ophthalmol. Vis. Sci., July 1, 2002; 43(7): 2442 - 2449. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. McKinnon, D. M. Lehman, L. A. Kerrigan-Baumrind, C. A. Merges, M. E. Pease, D. F. Kerrigan, N. L. Ransom, N. G. Tahzib, H. A. Reitsamer, H. Levkovitch-Verbin, et al. Caspase Activation and Amyloid Precursor Protein Cleavage in Rat Ocular Hypertension Invest. Ophthalmol. Vis. Sci., April 1, 2002; 43(4): 1077 - 1087. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Kortuem, L. K. Geiger, and L. A. Levin Differential Susceptibility of Retinal Ganglion Cells to Reactive Oxygen Species Invest. Ophthalmol. Vis. Sci., September 1, 2000; 41(10): 3176 - 3182. [Abstract] [Full Text] |
||||
![]() |
I. Nir, W. Kedzierski, J. Chen, and G. H. Travis Expression of Bcl-2 Protects against Photoreceptor Degeneration in retinal degeneration slow (rds) Mice J. Neurosci., March 15, 2000; 20(6): 2150 - 2154. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Katai and N. Yoshimura Apoptotic Retinal Neuronal Death by Ischemia-Reperfusion Is Executed by Two Distinct Caspase Family Proteases Invest. Ophthalmol. Vis. Sci., October 1, 1999; 40(11): 2697 - 2705. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |