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Journal of Neuroscience, Vol 10, 2996-3013, Copyright © 1990 by Society for Neuroscience
Ultrastructural localization of tyrosine hydroxylase in the rat ventral tegmental area: relationship between immunolabeling density and neuronal associations
VE Bayer and VM Pickel
Department of Neurology and Neurosciences, Cornell University Medical College, New York, New York 10021.
Dopaminergic neurons of the A 10 cell group in the rat ventral tegmental
area (VTA) exhibit electrical and dye coupling. Also, the activity of these
neurons at least partially reflects their content of tyrosine hydroxylase
(TH), the rate-limiting enzyme in catecholamine biosynthesis. We examined
the ultrastructural localization of TH to determine the morphological
features of dopaminergic neurons in the VTA and the relationships between
their TH immunoreactivity content and afferent input. Antiserum against the
trypsin-treated form of TH was localized using peroxidase-antiperoxidase
(PAP) and immunoautoradiographic methods. Immunoreactivity was detected in
perikarya, dendrites, and terminals. The perikarya contained the usual
organelles, as well as cilia, lamellar bodies, and subsurface cisterns.
Qualitative evaluation of peroxidase reaction product and quantitative
analysis of the number of silver grains/unit area revealed varying amounts
of TH immunoreactivity in nuclei and cytoplasm. Lightly or intensely
labeled nuclei were not necessarily associated with corresponding
cytoplasmic labeling density. However, cytoplasmic labeling directly
corresponded to the relative frequencies of neuronal appositions and
synaptic input. Those neurons with less dense cytoplasmic PAP product
received fewer synaptic contacts and were less frequently in apposition to
other TH-labeled soma and dendrites than neurons displaying relatively more
dense cytoplasmic PAP product. Analysis of single sections revealed that
67% (n = 71) of all TH- labeled somata and 15% (n = 2431) of all TH-labeled
dendrites were in apposition to other TH-labeled soma or dendrites.
TH-labeled terminals were rarely detected and contained relatively low
levels of immunoreactivity. The majority of labeled terminals (n = 29/46)
formed synapses with labeled soma and dendrites. Unlabeled terminals (n =
2424) in contact with TH-labeled dendrites appeared to form predominantly
symmetric synapses. Ten percent (n = 248) of the unlabeled terminals dually
synapsed onto adjacent immunoreactive dendrites, perikarya, or dendrite and
perikaryon. We conclude that in the rat VTA, (1) detected TH
immunoreactivity in cytoplasm, but not nucleus, corresponds to the level of
feedback principally from nondopaminergic afferents; (2) dendrodendritic as
well as axodendritic synapses between TH-immunoreactive neurons may mediate
dopaminergic autoinhibition; and (3) gap junction-like appositions between
neurons and convergent inputs from unlabeled terminals onto
TH-immunoreactive profiles provide an anatomical substrate whereby cellular
activities might be coordinated under certain conditions.
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