The Journal of Neuroscience, January 1, 2002, 22(1):73-81
Activity- and Target-Dependent Regulation of Large-Conductance
Ca2+-Activated K+ Channels in Developing Chick
Lumbar Motoneurons
Miguel
Martin-Caraballo and
Stuart
E.
Dryer
Department of Biology and Biochemistry, University of Houston,
Houston, Texas 77204-5513
The functional expression of large-conductance (BK-type)
Ca2+-activated K+
(KCa) channels was examined in developing chick
lumbar motoneurons (LMNs) between embryonic day 6 (E6) and E13 using
patch-clamp recording techniques. The macroscopic KCa
current of E13 LMNs is inhibited by iberiotoxin and resistant to
apamin. The average macroscopic KCa density was low before
E8 and increased 3.3-fold by E11, with an additional 1.8-fold increase
occurring by E13. BK-type KCa channels could not be
detected in inside-out patches from E8 LMNs but were readily detected
at E11. The density of voltage-activated Ca2+
currents did not change between E8 and E11. Surgical ablation of target
tissues at E5 caused a significant reduction in average KCa
density in LMNs measured at E11. Conversely, chronic in
ovo administration of D-tubocurarine, which causes
an increase in motoneuron branching on the surface of the muscle target
tissue, evoked a 1.8-fold increase in average LMN KCa
density measured at E11. Electrical activity also contributed to
developmental regulation of LMN KCa density. A significant
reduction in E11 KCa density was found after chronic
in ovo treatment with the neuronal nicotinic antagonist
mecamylamine or the GABA receptor agonist muscimol, agents that reduce
activation of LMNs in ovo. Moreover, 3 d exposure
to depolarizing concentrations of external K+ to
LMNs cultured at E8 caused an increase in KCa expression. Conversely, tetrodotoxin caused a decrease in KCa
expression in cultured E8 LMNs developing for 3 d in the presence
of neurotrophic factors that promote neuronal survival in the absence
of target tissues.
Key words:
motoneuron; development; Ca2+-activated K+ channels; slowpoke; electrical activity; trophic factors
Copyright © 2002 Society for Neuroscience 0270-6474/02/22173-09$05.00/0