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The Journal of Neurophysiology Vol. 84 No. 6 December 2000, pp. 2975-2983
Copyright ©2000 by the American Physiological Society
Department of Neurophysiology, Paul Flechsig Institute of Brain Research, University of Leipzig, D-04109 Leipzig, Germany
Bringmann, A.,
S. Schopf, and
A. Reichenbach.
Developmental Regulation of Calcium Channel-Mediated Currents in
Retinal Glial (Müller) Cells. J. Neurophysiol. 84: 2975-2983, 2000. Whole cell voltage-clamp
recordings of freshly isolated cells were used to study changes in the
currents through voltage-gated Ca2+ channels
during the postnatal development of immature radial glial cells into
Müller cells of the rabbit retina. Using
Ba2+ or Ca2+ ions as charge
carriers, currents through transient low-voltage-activated (LVA)
Ca2+ channels were recorded in cells from early
postnatal stages, with an activation threshold at
60 mV and a peak
current at
25 mV. To increase the amplitude of currents through
Ca2+ channels, Na+ ions
were used as the main charge carriers, and currents were recorded in
divalent cation-free bath solutions. Currents through transient LVA
Ca2+ channels were found in all radial glial
cells from retinae between postnatal days 2 and 37. The currents
activated at potentials positive to
80 mV and displayed a maximum at
40 mV. The amplitude of LVA currents increased during the first
postnatal week; after postnatal day 6, the amplitude remained virtually
constant. The density of LVA currents was highest at early postnatal
days (days 2-5: 13 pA/pF) and decreased to a stable, moderate level
within the first three postnatal weeks (3 pA/pF). A significant
expression of currents through sustained, high-voltage-activated
Ca2+ channels was found after the third postnatal
week in ~25% of the investigated cells. The early and sole
expression of transient currents at high-density may suggest that LVA
Ca2+ channels are involved in early developmental
processes of rabbit Müller cells.
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