R. Martinezmurillo et al., SUBCELLULAR-LOCALIZATION OF LOW-AFFINITY NERVE GROWTH-FACTOR RECEPTOR-IMMUNOREACTIVE PROTEIN IN ADULT-RAT PURKINJE-CELLS FOLLOWING TRAUMATIC INJURY, Experimental Brain Research, 119(1), 1998, pp. 47-57
Cerebellar Purkinje cells in the rat express low-affinity nerve growth
factor receptor (p75 NGFR) antigen during development, but rarely in
normal adult animals. In striking contrast, re-expression of p75 NGFR-
immunoreactive protein was reported by light microscopy immunocytochem
istry in adult rat Purkinje cells as early as I day after traumatic ax
otomy. Characteristically, varicose axons through the infraganglionic
zone were also stained. To date, however, there is no information on t
he subcellular location of the antigenic re-expression. To address thi
s, a pre-embedding immunocytochemical ultrastructural study using affi
nity-purified monoclonal 192-IgG was carried out after an experimental
ly induced traumatic lesion of the rat cerebellum. At the electron mic
roscopic level, immunostaining was intense in Purkinje cells. In these
cells, the immunoreactivity was always associated with the internal f
ace of the membranes of the rough endoplasmic reticulum, Golgi apparat
us and nuclear envelope. Patches of immunoreactivity were also associa
ted with the outer surface of the plasma membrane of the cell body, de
ndritic processes and axons. It is noteworthy that receptor immunoreac
tivity was detected in recurrent collaterals of Purkinje cell axons fo
rming symmetric synaptic contacts with the cell body and dendrites of
immunonegative local circuit neurons. Results of this study show that
injury-induced re-expression of p75 NGFR antigen is restricted to Purk
inje cells. Also, the relative importance of the contribution of the l
ocal circuit neurons to the production of neurotrophic substances afte
r trauma is suggested.