PKA holoenzyme is functionally coupled to CFTR by AKAPs

被引:43
作者
Huang, P
Trotter, K
Boucher, RC
Milgram, SL
Stutts, MJ
机构
[1] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, CF Pulm Res & Treatment Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 278卷 / 02期
关键词
cystic fibrosis transmembrane regulator; protein kinase A; adenosine; 3; 5 '-cyclic monophosphate; compartmentalization; A kinase anchoring proteins;
D O I
10.1152/ajpcell.2000.278.2.C417
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cystic fibrosis transmembrane regulator (CFTR) is reported to be preferentially regulated by membrane-bound protein kinase A (PKAII). We tested for close physical and functional association of PKA with CFTR in inside-out membrane patches excised from Calu-3 cells. In the presence of MgATP, 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (CPT-cAMP) increased the product of CFTR channel number and open probability (from 0.36 +/- 0.12 to 1.23 +/- 0.57, n = 20, P < 0.0025), and this stimulation was abolished by PKI. Thus Calu-3 membrane isolated from cells retains PKA holoenzyme that is functionally coupled to CFTR. PKAII is anchored at specific subcellular sites by A kinase anchoring proteins (AKAPs). Exposure of excised patches to HT-31, a peptide that disrupts the association of PKAII and AKAPs, prevented CPT-cAMP stimulation of CFTR. Therefore, PKA holoenzyme in isolated membrane patches is bound to AKAPs. In whole cell voltage-clamp studies, intracellular dialysis of Calu-3 cells with HT-31 blocked the activation of CFTR by extracellular adenosine. These results suggest that AKAPs mediate PKA compartmentalization with CFTR and are required for activation of CFTR by physiological regulators.
引用
收藏
页码:C417 / C422
页数:6
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