Growth of dendrites in the optic tectum of the chick embryo following destruction of the eye primordium.

The consequences of depriving the optic tectum of axons from the contralateral eye have been studied in Golgi-impregnated brains from a staged series of chick embryos. Following enucleation at 2–5 days of age, measurements of dendritic length and the numbers of branches at all orders for three cell types were performed with an automated three-dimensional tracking system at various survival times. Dendritic lengths and the number of middle order branches of neurons from control animals, aged 12–14 days (stages 38–40), are greater than those from non-innervated embryos of the same ages. However, by Day 18 (stage 44), no significant differences in length or branching are seen between neurons from control and experimental embryos. Observations of these neurons revealed qualitative differences between experimental and control embryos. Growth cones, varicosities and filopodia, indicators of dendritic differentiation, are more commonly associated with neurons from control Day 12 and 14 embryos, than operated embryos of the same stages. However, at Days 16 and 18 these growth characteristics are more usually seen on neurons from deafferented embryos than from controls.The deleterious effects observed in experimental animals between Days 12 and 14 are presumably caused by the absence of optic fibers. The eventual growth during late embryogenesis, of the cells deprived of optic input, may reflect a trophic influence not acting in the earlier period.