B. Krisch et al., VISUALIZATION OF NEUROPEPTIDE-BINDING SITES ON INDIVIDUAL TELENCEPHALIC NEURONS OF THE RAT, Cell and tissue research, 272(3), 1993, pp. 523-531
The identification of high-affinity binding sites for neuropeptides on
individual target cells is a prerequisite when studying the sites of
action and the manner in which peptides act as neuromediators. In situ
and in vitro, this can be achieved using newly synthesized, biologica
lly active conjugates of somatostatin or cholecystokinin (sulphated oc
tapeptide) with colloidal gold. Labelled neurons show a peptide-specif
ic, non-overlapping distribution in rat telencephalic structures; i.e,
whereas the somatostatin-gold conjugate labels binding sites on neuro
ns and glial cells, cholecystokinin-binding sites are restricted to ne
urons. Binding of either gold-labelled ligand can be competitively sup
pressed by excess amounts of the native peptide or its analogues. Neur
onal somatostatin-binding sites are visualized on neurons in lamina II
I and, in particular, in lamina V/VI of the primary somatosensory cort
ex and in the magnocellular nucleus of the telencephalic cholinergic s
ystem. Cholecystokinin-binding sites are localized in the main olfacto
ry bulb, on neurons in the cortical ''hindlimb'' and ''forelimb'' regi
on, in the hippocampus, and in the cingulate and visual cortex.