PURPOSE. Ectopic expression of Bcl-2 in photoreceptors of mice with retinal
degenerative disease slows progression of the disease. BAG-1 has previousl
y been shown to augment the inhibitory effect of Bcl-2 on programmed cell d
eath in cultured cell systems. This study was designed to determine whether
the coexpression of BAG-1 and Bcl-2 in the photoreceptors of mice with an
autosomal dominant form of retinitis pigmentosa (RP) would enhance the prot
ective effect provided by Bcl-2 alone.
METHODS. An expression vector using the 5' regulatory region of the murine
opsin gene was used to target the expression of BAG-1 specifically to photo
receptor cells of mice. The BAG-1 transgenic mice were crossed to Bcl-2 tra
nsgenics to obtain animals that coexpress the two transgenes in photorecept
or cells. BAG-1/Bcl-2 animals were then crossed to an RP mouse model (a tra
nsgenic line overexpressing the S334ter rhodopsin mutant) to assess the eff
ect of coexpression of BAG-1 and Bcl-2 on retinal degeneration. Morphologic
analysis was performed on retinas isolated at various times after birth to
monitor disease progression.
RESULTS. High levels of BAG-1 expression resulted in retinal degeneration t
hat was not prevented by Bcl-2 expression. However, coexpression of appropr
iate levels of BAG-1 and Bcl-2 was found to have a profound inhibitory effe
ct on retinal degeneration caused by overexpression of a mutant rhodopsin t
ransgene. Whereas expression of Bcl-2 alone was previously found to delay d
egeneration of the retina from 2 weeks to approximately 4 weeks of age, coe
xpression of BAG-1 and Bcl-2 inhibited photoreceptor cell death for as long
as 7 to 3 weeks.
CONCLUSIONS. The synergistic effect against photoreceptor cell death produc
ed by the coexpression of Bcl-2 and BAG-1 indicates that these proteins can
function in concert to prevent cell death. At the correct dosage, coexpres
sion of Bcl-2 and BAG-1 may serve as a potential means to treat retinal deg
enerative diseases.