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J Neurophysiol 82: 1627-1631, 1999;
0022-3077/99 $5.00
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The Journal of Neurophysiology Vol. 82 No. 3 September 1999, pp. 1627-1631
Copyright ©1999 by the American Physiological Society

RAPID COMMUNICATION

TGFbeta 1 Regulates the Gating Properties of Intermediate-Conductance KCa Channels in Developing Parasympathetic Neurons

Loic Lhuillier and Stuart E. Dryer

Department of Biology and Biochemistry, University of Houston, Houston, Texas 77204-5513

Lhuillier, Loic and Stuart E. Dryer. TGFbeta 1 Regulates the Gating Properties of Intermediate-Conductance KCa Channels in Developing Parasympathetic Neurons. J. Neurophysiol. 82: 1627-1631, 1999. The developmental expression of Ca2+-activated K+ channels (KCa) in chick ciliary ganglion (CG) neurons is regulated by a target-derived avian isoform of TGFbeta 1, which evokes a robust increase in the number of functional large-conductance (BK) KCa channels but which produces no change in their kinetics. However, CG neurons express multiple KCa channel subtypes. Here we show that TGFbeta 1 regulates the gating properties of intermediate-conductance (IK) KCa channels in developing CG neurons. IK channels in inside-out patches excised from control E9 CG neurons became active on exposure to 1-5 µM free Ca2+ but then remained active on return to Ca2+-free salines. In contrast, IK channels in TGFbeta 1-treated cells became active on exposure to 1-5 µM Ca2+, but became quiescent immediately on return to Ca2+-free salines. In contrast to its effects on BK channels, TGFbeta 1 had no effect on the mean number of IK channels detected in excised patches. IK channels were not activated in cell-attached patches on E9 neurons depolarized by bath application of 145 mM KCl in the presence of 5 mM external Ca2+. However, BK channels were activated immediately by this procedure and were detected at a higher density in TGFbeta 1-treated cells. In addition, analyses of macroscopic KCa fluctuations, and the voltage-dependence of KCa tail currents, suggest that IK channels do not contribute to voltage-evoked whole cell KCa. IK channels therefore may have some other function. These results indicate that the effects of TGFbeta 1 on CG neurons entail distinct actions on multiple KCa channel subtypes.




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