The broad array of K+ channels in epithelial cells includes voltage-de
pendent (mainly outward) and Ca2+-activated channels, and K+ channels
modulated by adenosine triphosphate (ATP). Voltage-dependent K+ channe
ls mediate Na+/K+ absorption and secretion; typically, they are found
in the basolateral membrane and exhibit burst activity. Ca2+-activated
K+ (Ca2+/K+) channels regulate activity by decreasing Ca2+ influx via
voltage-gated Ca2+ channels. Ca2+/K+ channels exhibit conductances of
4-300 pS, and have a low open probability (< 10(-7)) at the level of
the resting membrane potential. ATP-sensitive channels have been obser
ved mainly in insulin-secreting pancreatic beta-cells and in the urina
ry tract, where the open state is rapidly closed by ATP. The channels
are voltage-dependent, exhibit burst activity, and, in the case of the
urinary-tract cells, are Ca2+ dependent. Chemical compounds that sele
ctively open or block K+ channels have been exploited to characterize
channels found in different cells, but no opener or blocker has been f
ound that specifically affects only one type of K+ channel. Specialize
d model systems and recombinant techniques have led to a general under
standing of the structure of K+ channels, but many important details r
emain to be determined.