Dj. Bare et al., P59(FYN) IN RAT-BRAIN IS LOCALIZED IN DEVELOPING AXONAL TRACTS AND SUBPOPULATIONS OF ADULT NEURONS AND GLIA, Oncogene, 8(6), 1993, pp. 1429-1436
Expression of the c-fyn proto-oncogene was analysed in the developing
and adult rat brain by subcellular fractionation and immunocytochemist
ry using polyclonal antibodies specific for its protein product (p59fy
n). Immunoperoxidase staining revealed widespread localization of p59f
yn in developing axonal tracts throughout the fetal (E18) rat brain. f
yn immunoreactivity was not observed in most axon-rich regions of the
adult brain, but continued to be expressed at elevated levels in the a
dult olfactory and vomeronasal systems. At other sites in the adult ra
t brain, fyn immunoreactivity was restricted to cell bodies of neurona
l subpopulations, especially those in brain stem and hypothalamic nucl
ei, and to subpopulations of glial cells along axonal tracts in the me
dulla, optic nerve and white matter of the spinal cord. In the periphe
ral nervous system, fyn staining was also prominent in Schwann cells.
Subcellular fractionation of fetal and adult rat brain confirmed the i
mmunocytochemical localization, demonstrating an enrichment of p59fyn
in membranes from a fetal brain fraction containing nerve growth cones
, and lower levels in adult brain where there was only a small enrichm
ent in synaptosomal membranes. The developmental regulation of p59fyn
suggests that the fyn tyrosine kinase may serve separate cellular role
s in axonal growth and specialized functions of mature neurons and gli
a.