R. Bernard et al., NSE-BCL-2 TRANSGENIC MICE, A MODEL SYSTEM FOR STUDYING NEURONAL DEATHAND SURVIVAL, Developmental neuroscience, 19(1), 1997, pp. 79-85
Bcl-2 is a crucial regulator of cell survival and death. We have recen
tly demonstrated that transgenic mice overexpressing the human Bcl-2 p
rotein specifically in their neurons have an increased number of neuro
nal cells which can survive in tissue culture in the absence of neurot
rophic factors. In order to understand why only some neurons can be re
scued from developmental and neurotrophic factor deprivation-induced d
eath, we have studied the expression pattern of the transgene during e
mbryonic development and in adulthood. We have demonstrated that trans
gene expression starts in embryos at E12.5 and that only half of the s
ensory neurons of the dorsal root ganglia expressed detectable levels
of the human Bcl-2. These results may explain why only 40% of the sens
ory neurons survived in tissue culture in the absence of neurotrophic
factors.