Affaitati Adele, Cardone Luca, de Cristofaro Tiziana, Carlucci Annalisa, Ginsberg Michael D, Varrone Stelio, Gottesman Max E, Avvedimento Enrico V, Feliciello Antonio
Dipartimento di Biologia e Patologia Molecolare e Cellulare, BioGeM Consortium, Istituto di Endocrinologia ed Oncologia Sperimentale CNR, Facoltà di Medicina, Universitá Federico II, via S. Pansini 5, 80131 Napoli, Italy.
J Biol Chem. 2003 Feb 7;278(6):4286-94. doi: 10.1074/jbc.M209941200. Epub 2002 Nov 8.
A-Kinase anchor proteins (AKAPs) immobilize and concentrate protein kinase A (PKA) isoforms at specific subcellular compartments. Intracellular targeting of PKA holoenzyme elicits rapid and efficient phosphorylation of target proteins, thereby increasing sensitivity of downstream effectors to cAMP action. AKAP121 targets PKA to the cytoplasmic surface of mitochondria. Here we show that conditional expression of AKAP121 in PC12 cells selectively enhances cAMP.PKA signaling to mitochondria. AKAP121 induction stimulates PKA-dependent phosphorylation of the proapoptotic protein BAD at Ser(155), inhibits release of cytochrome c from mitochondria, and protects cells from apoptosis. An AKAP121 derivative mutant that localizes on mitochondria but does not bind PKA down-regulates PKA signaling to the mitochondria and promotes apoptosis. These findings indicate that PKA anchored by AKAP121 transduces cAMP signals to the mitochondria, and it may play an important role in mitochondrial physiology.
A激酶锚定蛋白(AKAPs)可将蛋白激酶A(PKA)亚型固定并浓缩于特定的亚细胞区室。PKA全酶在细胞内的靶向作用可引发靶蛋白的快速高效磷酸化,从而增强下游效应器对cAMP作用的敏感性。AKAP121将PKA靶向至线粒体的细胞质表面。在此我们表明,在PC12细胞中条件性表达AKAP121可选择性增强向线粒体的cAMP-PKA信号传导。AKAP121的诱导可刺激促凋亡蛋白BAD在Ser(155)位点发生PKA依赖性磷酸化,抑制细胞色素c从线粒体释放,并保护细胞免于凋亡。一种定位于线粒体但不结合PKA的AKAP121衍生突变体可下调向线粒体的PKA信号传导并促进凋亡。这些发现表明,由AKAP121锚定的PKA可将cAMP信号转导至线粒体,并且它可能在线粒体生理学中发挥重要作用。