Bcl-2 Overexpression Does Not EnhanceIn Vivo Axonal Regeneration of Retinal Ganglion Cells after Peripheral Nerve Transplantation in Adult Mice

Abstract

Optic nerve (ON) injury in adult mammals causes retinal ganglion cell (RGC) death and subsequent visual loss. Recovery of vision requires both rescuing axotomized RGCs and inducing their axonal regeneration. Axotomized RGCs are significantly rescued by overexpression of <i>bcl-2</i>, an anti-apoptotic gene. However, whether <i>bcl-2</i> affects axonal regeneration is controversial. In neonatal <i>bcl-2</i> transgenic mice (<i>bcl-2</i> mice), optic tract regeneration after tectal lesion was promoted (Chen et al., 1997), whereas ON regeneration after ON crush was not (Lodovichi et al., 2001). These conflicting results may be attributable to different environments between tectum and ON. We tested here whether <i>bcl-2</i> overexpression enhances<i>in vivo</i> RGC axonal regeneration in adult mice through a permissive environment in the peripheral nerve (PN) graft. Four weeks after PN transplantation to the proximal ON stump, we assessed the number of surviving and regenerating RGCs by retrograde labeling. Although the survival rate in <i>bcl-2</i> mice was significantly enhanced compared with that in wild-type (wt) mice, the regeneration rate was not enhanced. In both <i>bcl-2</i> and wt mice, RT97 immunostaining of the PN-grafted retinas revealed some RGC axons regrowing intraretinally but repulsed at the optic disk. To circumvent this repulsive barrier, we directly transplanted the PN graft to the partially injured retina and compared regeneration rates between these mice. Here again the regeneration rate in<i>bcl-2</i> mice did not exceed that in wt mice. These findings indicate that <i>bcl-2</i> overexpression enhances survival but not axonal regeneration of adult RGCs even within a permissive environment.