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Oxidant signaling underlies PKGIalpha modulation of Ca2 (show CA2 ELISA Kits)+ sparks and BKCa in myogenically active arterioles
These data outline a new signaling mechanism by which KCa1.1 regulates beta1-integrin function and therefore invasiveness of rheumatoid arthritis fibroblast-like synoviocytes (RA-FLSs).
These results provide further insights into the mechanism of modulation of the different N-terminal regions of the BKCa channel by beta-subunits.
Implicating both KCa1.1 and KCa3.1 (show KCNN4 ELISA Kits) channels.
These results identify KCa1.1 channels as crucial regulators of skeletal myogenesis.
Results show that reduced miR-17 expression is correlated with increased expression of KCNMA1 in malignant pleural mesothelioma. Computational analysis identified KCNMA1 gene is a direct target of miR-17.
Our report defines a novel autosomal recessive KCNMA1-related epileptic phenotype that encompasses cerebellar atrophy without paroxysmal dyskinesia, and highlights the sensitivity of the developing brain to both increased and decreased activity of the KCNMA1-encoded channels
A directed proteomic approach discovered the novel interaction of BKCa with Tom22 (show TOMM22 ELISA Kits), a component of the mitochondrion outer membrane import system, and the adenine nucleotide translocator (show SLC25A4 ELISA Kits) (ANT).
GSK3b (show GSK3b ELISA Kits) may up-regulate BK channels, an effect disrupted by lithium or additional expression of AKT (show AKT1 ELISA Kits) and possibly participating in the regulation of cell volume and excitability.
MiR (show MLXIP ELISA Kits)-31 represses KCNMA1 expression.
High cholesterol can reduce the protein expression of BK channel beta1 subunit in rabbit Oddi's sphincter (SO) cells which suggests high cholesterol can affect the function of BKca channel [BK channel beta1 subunit]
Aldosterone does not contribute to the regulation of BK channel expression/activity in response to dietary K(+) loading.
Slo1 channels in the lysosome are required for refilling lysosomal Ca(2 (show CA2 ELISA Kits)+) stores.
Dynamic coupling between TRPV4 (show TRPV4 ELISA Kits) and Ca(2 (show CA2 ELISA Kits)+)-activated SK1 (show SPHK1 ELISA Kits)/3 and IK1 (show KCNN4 ELISA Kits) K(+) channels plays a critical role in regulating the K(+)-secretory BK channel KCNMA1 in kidney collecting duct cells.
The differential regulation of ROMK (show KCNJ1 ELISA Kits), large-conductance Ca(2 (show CA2 ELISA Kits)+)-activated K(+) (BK) channel, BK-alpha and NKCC2 (show SLC12A1 ELISA Kits) between female and male mice, at least, were partly mediated via WNK1 (show WNK1 ELISA Kits) pathway, which may contribute to the sexual dimorphism of plasma K(+) and blood pressure control.
KCNMA1 contributes to the regulation of insulin (show INS ELISA Kits) signalling in mature adipocytes
Results showed that BK-knockout osteoblasts displayed low proliferation and impaired mineralization ability providing further evidence that BK channel is critical for osteoblast function.
Data, including data from studies in knockout mice, suggest that association/disassociation of subunits Kcnma1 and Kcnab1 (show KCNAB1 ELISA Kits) of the BK channel (large-conductance calcium-activated potassium channel (show KCNAB2 ELISA Kits)) is involved in function of coronary artery smooth muscle cells and their dysfunction during ischemia/reperfusion-induced myocardial injury in diabetes.
This study demonstrated that The interaction of MaxiK channel with GAT3 (show SLC6A13 ELISA Kits) opens the possibility of a role of MaxiK channel in GABA homeostasis and signaling.
the enhanced effect of amiloride on potassium secretion in wild-type compared to knockout mice on the alkaline diet clarify a BK- alpha/beta4-mediated potassium secretory pathway in intercalated cells driven by ENaC (show SCNN1A ELISA Kits)-mediated sodium reabsorption
Data suggest that the ion channels CaV1.3, bestrophin-1 and maxiK were identified as players in the regulation of photoreceptor outer segments (POS) phagocytosis by the retinal pigment epithelium (RPE).
analysis of SLO3 K+ channels shows evolutionary divergence for an RCK1 region of critical function
A neural-specific splice-variant exon of Slo serves as a gain-of-function module and allows physiologically relevant levels of membrane potential and intracellular calcium to activate the resultant channel effectively during Xenopus embryogenesis.
Porcine K2P3.1 (show KCNK3 ELISA Kits) channels exhibit atrial expression and functional properties similar to their human orthologs, supporting a general role as antiarrhythmic drug targets.
Inositol trisphosphate is an activator of BKCA channels in porcine coronary smooth muscle cells and exerts a coronary artery-relaxing effect.
Testerone-induced relaxation of endothelium-denuded coronary arteries is mediated, at least in part, by enhanced NO production, leading to cGMP synthesis and PKG (show PRKG1 ELISA Kits) activation, which, in turn, opens BK(Ca) channels.
Removal of element 6b from the endogenous slo gene affected the production of functional ethanol tolerance in an ethanol-vapor recovery from sedation assay.
SLO2 (show KCNT1 ELISA Kits) Channels Are Inhibited by All Divalent Cations That Activate SLO1 K+ Channels
Slo mutant larvae exhibit alterations in synapse morphology, active zone size and neurotransmission that are similar to dysc mutants.
Results show using the Drosophila model organism, we demonstrate a central role for the BK-type Ca(2+) -activated K(+) channel gene slo in the production of alcohol withdrawal seizures
Here we examined the action of docosahexaenoic acid on the Slo1 channel without any auxiliary subunit and sought to elucidate the biophysical mechanism and the molecular determinants of the DHA sensitivity.
Our work identifies a Drosophila homolog of a deaf-blindness gene as a new component of the circadian output pathway,termed DYSC(dyschronic) whish expressed in major neuronal tracts and regulates expression of SLOWPOKE (SLO)
Results propose that modulation of SLO by SLOB regulates neurotransmission in mNSCs, influencing downstream insulin (show INS ELISA Kits) pathway signaling and metabolism.
monomeric D14-3-3zeta (show YWHAZ ELISA Kits) is capable of modulating dSlo channel activity in this regulatory complex.
synaptic strength and synaptic strength at neuromuscular junctions along the dorsal-ventral differentials at physiological Ca(2+) levels were not significantly altered in slowpoke (slo) and Shaker (Sh) mutants
MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit, which is the product of this gene, and the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified.
BK channel alpha subunit
, BKCA alpha subunit
, calcium-activated potassium channel subunit alpha-1
, calcium-activated potassium channel, subfamily M subunit alpha-1
, maxi-K channel HSLO
, slo homolog
, slowpoke homolog
, stretch-activated Kca channel
, calcium-activated potassium channel subunit alpha 1
, BK channel
, BKCA alpha
, large conductance calcium-activated potassium channel alpha subunit
, maxi K channel
, calcium-activated potassium channel alpha subunit
, MaxiK calcium-activated potassium channel
, calcium activated potassium channel protein
, large conductance calcium-activated potassium (BK) channel alpha subunit a
, potassium large conductance calcium-activated channel, subfamily M, alpha member 1
, large conductance calcium-activated potassium channel subfamily M alpha member 1
, pulmonary calcium activated potassium channel
, calcium-activated potassium channel subunit alpha-1-like
, large calcium-activated potassium channel alpha member 1
, CG10693 gene product from transcript CG10693-RS
, Maxi K channel