E. Simburger et al., Distribution of the receptor-anchoring protein gephyrin in the rat dentategyrus and changes following entorhinal cortex lesion, CEREB CORT, 10(4), 2000, pp. 422-432
We analyzed the distribution of the receptor-anchoring protein gephyrin in
the normal and deafferented rat dentate gyrus to investigate whether the ex
pression of this postsynaptic protein is altered in response to the formati
on of new synaptic contacts. Confocal microscopy and digital image analysis
revealed that in normal dentate gyrus immunolabeling was most prominent in
the outer molecular layer and decreased successively in the direction of t
he granule cell layer. Simultaneous immunolabeling for gephyrin and cell-sp
ecific markers showed that granule cells and parvalbumin positive interneur
ons express gephyrin. Large, intensely stained, gephyrin-positive clusters
were distributed along distinct dendrites, and most of them were positive f
or parvalbumin. Calbindin-immunostained dendrites were associated with smal
ler, gephyrin-positive clusters. Lesion of the medial entorhinal cortex lea
ds to deafferentiation of the middle molecular layer which resulted in an i
ncreased gephyrin immunoreactivity. These changes were due to a significant
ly increased concentration of the very small gephyrin-positive clusters. Pa
rvalbumin-positive dendrites did not display any increase in co-localizing
gephyrin-positive structures. The altered immunolabeling pattern persisted
until 12 weeks after lesion, a time when the process of synaptic reorganiza
tion is complete. Our findings suggest that synaptogenesis following deaffe
rentiation results in a cell-specific redistribution of gephyrin immunoreac
tivity at specific inhibitory synapses.