Genetic evidence for cell death mediated by nerve growth factor and the neurotrophin receptor p75 in the developing mouse retina and spinal cord

The role of nerve growth factor (NGF) and of the neurotrophin receptor p75 (p75(NTR)) in programmed cell death was investigated in the retina and the spinal cord of mouse embryos. Large numbers of cells express p75NTR in and along the developing optic nerve and in the mantle zone of the spinal cord. In embryos carrying deletions in the ngf or the p75(NTR) gene, cell death was reduced in the retina and in the spinal cord. Increased numbers of Isle t-1-immunoreactive cells were detected in the dorsal spinal cord, and the m antle zone was enlarged in both mutants. These results indicate that NGF/p7 5(NTR)-dependent mechanisms are used to remove cells when axonal tracts elo ngate in developing neuroepithelia.