N. Hajos et al., TARGET SELECTIVITY AND NEUROCHEMICAL CHARACTERISTICS OF VIP-IMMUNOREACTIVE INTERNEURONS IN THE RAT DENTATE GYRUS, European journal of neuroscience, 8(7), 1996, pp. 1415-1431
Vasoactive intestinal polypeptide (VIP) has been shown to be present i
n a morphologically heterogeneous subpopulation of interneurons in the
dentate gyrus, but the relationship between their input and output ch
aracteristics and neurochemical features has not been established. Thr
ee types of VIP-immunoreactive cells have been identified on the basis
of these criteria: (i) cells forming a dense axonal plexus in the hil
us have always coexisted with the calcium binding protein calretinin (
CR), but never with the neuropeptide cholecystokinin (CCK). The postsy
naptic targets of these VIP-positive cells were neurons visualized by
immunostaining for substance P receptor, which is known to label diffe
rent hilar non-principal cells. (ii) VIP-immunoreactive basket cells,
innervating predominantly the somata and proximal dendrites of granule
cells, were found in the stratum moleculare and stratum granulosum. T
hey contained CCK, but not CR. (iii) Cells projecting to the stratum m
oleculare were found to have dendrites and axons restricted to this la
yer. In 75% of these cells VIP coexisted with CR but not with CCK, and
they established multiple contacts largely with non-principal cells.
GABA was shown to be present but the calcium-binding proteins calbindi
n D28K and parvalbumin were absent in all three types of VIP-containin
g interneuron. On the basis of these observations we conclude that thr
ee different types of VIP-positive neuron are present in this area, an
d are likely to subserve different inhibitory functions: cells with a
hilar projection as well as those projecting to the stratum moleculare
may synchronize the activity of hilar and other interneurons, or disi
nhibit granule cells by specific interneuron-to-interneuron connection
s. In contrast, basket cells control the activity of granule cells dir
ectly, via perisomatic inhibition.