Polycystin-1 activates the Calcineurin/NFAT (nuclear factor of activated T-cells) signaling pathway

被引:81
作者
Puri, S
Magenheimer, BS
Maser, RL
Ryan, EM
Zien, CA
Walker, DD
Wallace, DP
Hempson, SJ
Calvet, JP
机构
[1] Univ Kansas, Med Ctr, Dept Biochem & Mol Biol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Internal Med, Kansas City, KS 66160 USA
[3] Univ Kansas, Med Ctr, Kidney Inst, Kansas City, KS 66160 USA
[4] Panjab Univ, Dept Biochem, Chandigarh 160014, India
关键词
D O I
10.1074/jbc.M402905200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of intracellular Ca2+ mobilization has been associated with the functions of polycystin-1 (PC1) and polycystin-2 (PC2), the protein products of the PKD1 and PKD2 genes. We have now demonstrated that PC1 can activate the calcineurin/NFAT ( nuclear factor of activated T-cells) signaling pathway through Galpha(q)-mediated activation of phospholipase C ( PLC). Transient transfection of HEK293T cells with an NFAT promoter-luciferase reporter demonstrated that membrane-targeted PC1 constructs containing the membrane proximal region of the C-terminal tail, which includes the heterotrimeric G protein binding and activation domain, can stimulate NFAT luciferase activity. Inhibition of glycogen synthase kinase-3beta by LiCl treatment further increased PC1-mediated NFAT activity. PC1-mediated activation of NFAT was completely inhibited by the calcineurin inhibitor, cyclosporin A. Cotransfection of a construct expressing the Galpha(q) subunit augmented PC1-mediated NFAT activity, whereas the inhibitors of PLC (U73122) and the inositol trisphosphate and ryanodine receptors (xestospongin and 2-aminophenylborate) and a nonspecific Ca2+ channel blocker (gadolinium) diminished PC1-mediated NFAT activity. PC2 was not able to activate NFAT. An NFAT-green fluorescent protein nuclear localization assay demonstrated that PC1 constructs containing the C-tail only or the entire 11-transmembrane spanning region plus C-tail induced NFAT-green fluorescent protein nuclear translocation. NFAT expression was demonstrated in the M-1 mouse cortical collecting duct cell line and in embryonic and adult mouse kidneys by reverse transcriptase-PCR and immunolocalization. These data suggest a model in which PC1 signaling leads to a sustained elevation of intracellular Ca2+ mediated by PC1 activation of Galpha(q) followed by PLC activation, release of Ca2+ from intracellular stores, and activation of store-operated Ca2+ entry, thus activating calcineurin and NFAT.
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收藏
页码:55455 / 55464
页数:10
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