Jw. Sechrist et al., AGE-DEPENDENT NEUROTRANSMITTER PLASTICITY OF CILIARY GANGLION NEURONS, Molecular and cellular neurosciences (Print), 12(4-5), 1998, pp. 311-323
We have examined neurotransmitter plasticity in postmitotic cholinergi
c neurons isolated from 6.5- to 11-day-old embryonic quail ciliary gan
glia. Purified neurons were labeled with Dil, transplanted into the tr
unk of young chick embryos, and assayed for catecholamine content and
[H-3]thymidine uptake 4 to 5 days later. For ciliary neurons derived f
rom 6.5- to 8-day-old embryos, as many as 25% (average of 9% overall)
expressed catecholamines in the host sympathetic ganglia, migratory st
ream, aortic plexuses, and adrenal medulla. In contrast, neurons from
>8-day-old ganglia did not acquire or produce detectable catecholamine
s, indicating a limited time period over which phenotypic conversion c
an occur in vivo. As a control, ciliary neurons were also injected int
o the head mesenchyme of young embryos; no catecholamine expression wa
s observed. Interestingly, after transplantation some Dil-labeled post
mitotic ciliary neurons took up [H-3]thymidine with or without phenoty
pic change. These results suggest that phenotypic plasticity in ciliar
y neurons is age-dependent, is location-dependent, and may involve res
umption of DNA replication, a characteristic feature of some different
iating adrenergic sympathetic neurons. Apoptosis of a few proliferatin
g transplanted cells may be induced independently or in association wi
th transmitter change.