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Two-Pore Domain Potassium Channels: Vascular Control by a
Newly Discovered Channel Family
Sponsored by
APS Cardiovascular Section
Ion Channels Track
Tuesday, May 1 — 10:30 AM-12:30 PM
Washington, DC Convention Center — Room 145A
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| Chaired: |
Robert M. Bryan, Jr., Baylor Col. of
Med.
Arthur Weston, Univ. of Manchester |
Potassium (K)
channels in vascular smooth muscle and endothelium are important
regulators of vascular function including the control of vessel tone.
Until recently the K channels studied in vascular cells have been
members of either the inwardly rectifying K channel family or the
voltage/Ca –gated K channel family. Members of the inwardly rectifying K
channel family include inwardly rectifying (Kir) and the
ATP-sensitive (KATP) K channels. Members of the voltage/Ca
–gated K channel family include Ca-activated (KCa) and
voltage sensitive or delayed rectifier (Kv) K channels. In
the last 10 years, a third family of K channels, 2P domain K channels (K2P),
has been discovered and cloned. This family of channels is distinct in
that each protein subunit has two pore or P domains unlike channels in
the other two families which have only one P domain for each subunit.
Currently, we now recognize that there are at least 12 genes coding for
functional K2P channels. Depending on the individual family
member, K2P can be regulated by one or more of the following:
pH, temperature, mechanical perturbation, anesthetics, arachidonic acid
and other poly-unsaturated fatty acids, DAG, PIP2,
phospholipids, G proteins, PKG, PKC, PKA, and casein kinase.
K2P
are found in virtually all tissues and organs throughout the body and are
being shown to have important roles in the regulation of physiological
processes. While message and/or protein for most of the K2P
channels have been reported in blood vessels, we are only beginning to
demonstrate their role in regulating vascular function. Given the diversity
of expression in vessels and the importance already demonstrated, the
recognition of K2P channels as major regulators of function will
certainly grow.
This symposium will bring together researchers who have
studied vascular K2P channels in a single forum with the
purpose of (1) introducing this newly discovered class of K channels to
biologists (2) demonstrating that 2P domain K channels have a major role
in controlling vascular function, and (3) demonstrating potential new
targets for therapeutic intervention during pathological
states. In this symposium, Michel Lazdunski will give an overview of the
K2P channels and discuss a neuroprotective role for K2P
channels following stroke and seizure. Alison Gurney
will discuss the role of K2P channels in setting the resting
membrane potential in pulmonary arteries and their involvement during
hypoxic conditions. Gillian Edwards will highlight the widespread
distribution of K2P channels in vascular myocytes and
endothelial cells. She will show how extracellular pH changes, together
with pharmacological and siRNA approaches can be used to investigate the
importance of these channels not only in blood vessels, but also in the
airways and urinary bladder. Robert Bryan will discuss a role for
K2P channels in dilations of cerebral arteries. This
symposium brings together the major scientists who are presently
investigating the critical importance of K2P in the
circulation and other systems. The symposium will update anyone
interested in vascular smooth muscle, vascular control, and/or novel K
channels.
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10:30 AM |
2P K channels: an overview and their role in
neuroprotection.
Michel Lazdunski, CNRS, Valbonne
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11:05 AM |
The regulation of pulmonary artery tone by 2P K
channels.
Alison M. Gurney, Univ. of Manchester
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11:30 AM |
Effects of pH and pharmacological modulation on
vascular tone: a role for 2P K channels.
Gillian Edwards,
Univ. of Manchester
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11:55 PM |
Cerebral artery dilations by 2P K channels.
Robert M. Bryan, Baylor Col. of Med.
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