Axonal Target Choice and Dendritic Development of Ferret Beta Retinal Ganglion Cells

TY - JOUR

T1 - Axonal Target Choice and Dendritic Development of Ferret Beta Retinal Ganglion Cells

AU - Wingate, R J

AU - Thompson, I D

AU - Wingate, Richard

PY - 1995/4/1

Y1 - 1995/4/1

N2 - We have investigated the relationship between axon targeting and dendritic morphology in beta retinal ganglion cells in the postnatal ferret. Axonal projections were assessed by making separate injections of different fluorescent retrograde tracers into either the superior colliculus or lateral geniculate nucleus in vivo. The dendritic morphology of retrogradely labelled cells was revealed by the in vitro intracellular injection of lucifer yellow in fixed retina. In this way, 405 retinal ganglion cells were triple- or double-labelled and characterized by their dendritic branching styles. Both the distinct dendritic morphology of beta cells and the characteristic restriction of their adult axonal terminals to the lateral geniculate nucleus emerge postnatally. Beta cell dendritic morphology is established between postnatal days 5 and 9. As in the cat (Ramoa et al., 1989), beta cells extend and then retract a projection to the superior colliculus as part of their normal development. Transient beta axonal collaterals to the superior colliculus persist beyond the period of cell death, but nearly all are withdrawn by postnatal day 15. No dendritically distinct beta cell projects to the superior colliculus alone, at any age. Heterochronic injections of different colours of retrograde tracer into the superior colliculus were used to study changes in the complement of the retinocollicular projection over time. A significant proportion of cells (58%) labelled at postnatal day 0 from the superior colliculus, which subsequently survived the period of cell death, were found to be beta cells that could no longer be demonstrated to have a retinocollicular axon.(ABSTRACT TRUNCATED AT 250 WORDS)

AB - We have investigated the relationship between axon targeting and dendritic morphology in beta retinal ganglion cells in the postnatal ferret. Axonal projections were assessed by making separate injections of different fluorescent retrograde tracers into either the superior colliculus or lateral geniculate nucleus in vivo. The dendritic morphology of retrogradely labelled cells was revealed by the in vitro intracellular injection of lucifer yellow in fixed retina. In this way, 405 retinal ganglion cells were triple- or double-labelled and characterized by their dendritic branching styles. Both the distinct dendritic morphology of beta cells and the characteristic restriction of their adult axonal terminals to the lateral geniculate nucleus emerge postnatally. Beta cell dendritic morphology is established between postnatal days 5 and 9. As in the cat (Ramoa et al., 1989), beta cells extend and then retract a projection to the superior colliculus as part of their normal development. Transient beta axonal collaterals to the superior colliculus persist beyond the period of cell death, but nearly all are withdrawn by postnatal day 15. No dendritically distinct beta cell projects to the superior colliculus alone, at any age. Heterochronic injections of different colours of retrograde tracer into the superior colliculus were used to study changes in the complement of the retinocollicular projection over time. A significant proportion of cells (58%) labelled at postnatal day 0 from the superior colliculus, which subsequently survived the period of cell death, were found to be beta cells that could no longer be demonstrated to have a retinocollicular axon.(ABSTRACT TRUNCATED AT 250 WORDS)

KW - Animals

KW - Animals, Newborn

KW - Autoradiography

KW - Axons

KW - Cell Death

KW - Cerebral Decortication

KW - Dendritic Cells

KW - Ferrets

KW - Geniculate Bodies

KW - Retinal Ganglion Cells

KW - Superior Colliculi

KW - Visual Pathways

M3 - Article

C2 - 7620621

SN - 0953-816X

VL - 7

SP - 723

EP - 731

JO - European Journal of Neuroscience

JF - European Journal of Neuroscience

IS - 4

ER -