The Journal of Neuroscience, December 15, 1998, 18(24):10481-10492
Expression Pattern and Neurotrophic Role of the
c-fms Proto-Oncogene M-CSF Receptor in Rodent Purkinje
Cells
Shin-ichi
Murase1 and
Yokichi
Hayashi2
1 Department of Anatomy, Keio University School of
Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan,
and 2 Department of Cell and Molecular Biology, Nagano
College of Nursing, Akoho 1694, Komagane-shi, Nagano
399-4117, Japan
To investigate whether the c-fms proto-oncogene
plays a role in the CNS, we examined its expression in mouse
brain. We found that c-fms-positive Purkinje cells first
appeared in caudal cerebellum at postnatal day 0 (P0) arranged
in a parasagittal manner, and most Purkinje cells gradually became
positive by P6. This differential expression was not seen from P7 to
adulthood, and the parasagittal pattern until P5 was different from
those of L7, zebrins, and the integrin
1 subunit. No neuronal
expression of c-fms was found in the other brain regions
examined. In both reeler and weaver mutant mice in the adult stage, all
Purkinje cells were positive for c-fms as in the
wild-type controls; however, the parasagittal bands of
c-fms-positive Purkinje cells were observed even in the adult staggerer mutant. To check the neurotrophic effect of macrophage colony-stimulating factor (M-CSF), we immunostained cerebella derived
from osteopetrotic mutant mice, that is, those devoid of active M-CSF.
We found that the number of calbindin-positive Purkinje cells in a
given cerebellum began to decrease substantially during the initial
4-5 weeks of the postnatal period. In addition, cultured Purkinje
cells were dependent on M-CSF for their survival. These data suggest
that expression of the c-fms gene is intrinsically programmed in the Purkinje cells and never affected by the afferent synaptic input and that neuronal survival of Purkinje cells is dependent on M-CSF after weaning. Therefore, c-fms is
considered to be a new developmental marker for Purkinje cells.
Key words:
granule cell; parallel fiber; neurotrophin; cytokine; microglia; integrin; zebrin; parasagittal band; CSF-1; retinoic acid
receptor-related orphan nuclear receptor
Copyright © 1998 Society for Neuroscience 0270-6474/98/182410481-12$05.00/0