Previously we described a transgenic mouse model in which neurofilaments ar
e sequestered in neuronal cell bodies and withheld from the axonal compartm
ent. This model and other transgenic models with disrupted neurofilaments a
re used widely to investigate the role of the neurofilament cytoskeleton in
normal neurons and in inherited or acquired diseases. To interpret such st
udies, it is important to establish whether the maldistribution of neurofil
aments has major secondary consequences on the cell biology of the affected
neurons. Notably, multiple perturbations of the nervous system simultaneou
sly affect both the neuronal cytoskeleton and neurotrophin expression. To d
etermine whether the expression of neurotrophic factors or their receptors
is perturbed by a primary disruption in neurofilaments, we compared the acc
umulated mRNA levels for ciliary neuroptrophic factor (CNTF), nerve growth
factor, neurotrophin 3, and the alpha CNTF receptor in mature transgenic mi
ce and their littermate controls. Consistently with the prolonged survival
of neurons expressing atypical or abnormally distributed neurofilaments, no
obvious changes were observed for any of the mRNA species examined. (C) 20
01 Wiley-Liss, Inc.