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The Journal of Neuroscience, February 15, 2002, 22(4):1290-1302
Ih Channels Contribute to the
Different Functional Properties of Identified Dopaminergic
Subpopulations in the Midbrain
Henrike
Neuhoff*,
Axel
Neu*,
Birgit
Liss, and
Jochen
Roeper
Medical Research Council, Anatomical Neuropharmacology Unit,
Department of Pharmacology, Oxford University, OX1 3TH United
Kingdom
Dopaminergic (DA) midbrain neurons in the substantia nigra (SN) and
ventral tegmental area (VTA) are involved in various brain functions
such as voluntary movement and reward and are targets in disorders such
as Parkinson's disease and schizophrenia. To study the functional
properties of identified DA neurons in mouse midbrain slices, we
combined patch-clamp recordings with either neurobiotin cell-filling
and triple labeling confocal immunohistochemistry, or single-cell
RT-PCR. We discriminated four DA subpopulations based on anatomical and
neurochemical differences: two calbindin D28-k
(CB)-expressing DA populations in the substantia nigra (SN/CB+) or
ventral tegmental area (VTA/CB+), and respectively, two calbindin D28-k negative DA populations (SN/CB , VTA/CB ). VTA/CB+
DA neurons displayed significantly faster pacemaker frequencies with
smaller afterhyperpolarizations compared with other DA neurons. In
contrast, all four DA populations possessed significant differences in
Ih channel densities and
Ih channel-mediated functional properties like sag amplitudes and rebound delays in the following order: SN/CB
VTA/CB SN/CB+ VTA/CB+. Single-cell RT-multiplex PCR
experiments demonstrated that differential calbindin but not calretinin
expression is associated with differential
Ih channel densities. Only in SN/CB DA
neurons, however, Ih channels were actively
involved in pacemaker frequency control. In conclusion, diversity
within the DA system is not restricted to distinct axonal projections
and differences in synaptic connectivity, but also involves differences
in postsynaptic conductances between neurochemically and
topographically distinct DA neurons.
Key words:
HCN channels; dopamine; calbindin; substantia nigra; ventral tegmental area; pacemaker; Parkinson's disease; confocal
immunohistochemistry; single-cell RT-PCR
*
H.N. and A.N. contributed equally to this work.
Correspondence should be addressed to Dr. Jochen Roeper, Medical
Research Council, Anatomical Neuropharmacology Unit, Oxford University,
Mansfield Road, Oxford OX1 3TH, UK. E-mail:
jochen.roeper{at}pharm.ox.ac.uk.
H. Neuhoff's present address: Scientific Services, Morphology, Zentrum
für Molekulare Neurobiologie Hamburg, D-20251 Hamburg, Germany.
A. Neu's present address: Institute for Neural Signaltransduction,
Zentrum für Molekulare Neurobiologie Hamburg, D-20251 Hamburg, Germany.
Copyright © 2002 Society for Neuroscience 0270-6474/02/2241290-13$05.00/0
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