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The Journal of Neuroscience, December 15, 1998, 18(24):10398-10408
Heteromultimeric Delayed-Rectifier K+ Channels in
Schwann Cells: Developmental Expression and Role in Cell
Proliferation
Alexander
Sobko1,
Asher
Peretz1,
Orian
Shirihai2,
Sarah
Etkin1,
Vera
Cherepanova1,
Daniel
Dagan2, and
Bernard
Attali1
1 Neurobiology Department, Weizmann Institute of
Science, Rehovot 76100, Israel, and 2 Bruce Rappaport
Faculty of Medicine, Bernard Katz Minerva Center for Cell Biophysics,
Technion, Haifa 31096, Israel
Schwann cells (SCs) are responsible for myelination of nerve fibers
in the peripheral nervous system. Voltage-dependent
K+ currents, including inactivating A-type
(KA), delayed-rectifier (KD), and inward-rectifier
(KIR) K+ channels,
constitute the main conductances found in SCs. Physiological studies
have shown that KD channels may play an
important role in SC proliferation and that they are downregulated in
the soma as proliferation ceases and myelination proceeds. Recent
studies have begun to address the molecular identity of
K+ channels in SCs. Here, we show that a large
repertoire of K+ channel subunits of the
Shaker (Kv1.1, Kv1.2, Kv1.4, and Kv1.5), Shab (Kv2.1), and Shaw (Kv3.1b and Kv3.2)
families is expressed in mouse SCs and sciatic nerve. We characterized
heteromultimeric channel complexes that consist of either Kv1.5 and
Kv1.2 or Kv1.5 and Kv1.4. In postnatal day 4 (P4) sciatic nerve,
most of the Kv1.2 channel subunits are involved in heteromultimeric
association with Kv1.5. Despite the presence of Kv1.1 and Kv1.2 subunits, the K+ currents were unaffected by
dendrotoxin I (DTX), suggesting that DTX-sensitive channel complexes do
not account substantially for SC KD
currents. SC proliferation was found to be potently blocked by
quinidine or 4-aminopyridine but not by DTX. Consistent with previous
physiological studies, our data show that there is a marked
downregulation of all KD channel subunits from P1-P4 to P40 in the sciatic nerve. Our results suggest
that KD currents are accounted for by a
complex combinatorial activity of distinct K+
channel complexes and confirm that KD
channels are involved in SC proliferation.
Key words:
K+ channels; Schwann cells; myelination; proliferation; development; ion channels; heteromultimeric
association
Copyright © 1998 Society for Neuroscience 0270-6474/98/182410398-11$05.00/0
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