학술논문

NFATc3 regulates BK channel function in murine urinary bladder smooth muscle.
Document Type
Article
Source
American Journal of Physiology: Cell Physiology. Sep2008, Vol. 295 Issue 3, pC611-C623. 13p. 9 Graphs.
Subject
*BLADDER
*SMOOTH muscle
*T cells
*TRANSCRIPTION factors
*PROTEINS
*ION channels
*LABORATORY mice
Language
ISSN
0363-6143
Abstract
The nuclear factor of activated T-cells (NFAT) is a Ca2+-dependent transcription factor that has been reported to regulate the expression of smooth muscle contractile proteins and ion channels. Here we report that large conductance Ca2+-sensitive potassium (BK) channels and voltage-gated K+ (Kv) channels may be regulatory targets of NFATc3 in urinary bladder smooth muscle (UBSM). UBSM myocytes from NFATc3-null mice displayed a reduction in iberiotoxin (IBTX)-sensitive BK currents, a decrease in mRNA for the pore-forming α-subunit of the BK channel, and a reduction in BK channel density compared with myocytes from wild-type mice. Tetraethylammonium chloride-sensitive K+ currents were elevated in UBSM myocytes from NFATc3-null mice, as was mRNA for the Shab family member Kv2.1. Despite K+ current upregulation, bladder strips from NFATc3-null mice displayed an elevated contractile response to electrical field stimulation relative to strips from wild-type mice, but this difference was abrogated in the presence of the BK channel blocker IBTX. These results support a role for the transcription factor NFATc3 in regulating UBSM contractility, primarily through an NFATc3-dependent increase in BK channel activity. [ABSTRACT FROM AUTHOR]