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钙/钙调蛋白依赖性激酶(CaMK)信号通过 CaMKI 和 AMP 激活的蛋白激酶参与自噬起始时 WIPI-1 的调节。

Ca2+/calmodulin-dependent kinase (CaMK) signaling via CaMKI and AMP-activated protein kinase contributes to the regulation of WIPI-1 at the onset of autophagy.

机构信息

Autophagy Laboratory, Interfaculty Institute for Cell Biology, Eberhard Karls University Tuebingen, Tuebingen, Germany.

出版信息

Mol Pharmacol. 2011 Dec;80(6):1066-75. doi: 10.1124/mol.111.071761. Epub 2011 Sep 6.

Abstract

Autophagy is initiated by multimembrane vesicle (autophagosome) formation upon mammalian target of rapamycin inhibition and phosphatidylinositol 3-phosphate [PtdIns(3)P] generation. Upstream of microtubule-associated protein 1 light chain 3 (LC3), WD-repeat proteins interacting with phosphoinositides (WIPI proteins) specifically bind PtdIns(3)P at forming autophagosomal membranes and become membrane-bound proteins of generated autophagosomes. Here, we applied automated high-throughput WIPI-1 puncta analysis, paralleled with LC3 lipidation assays, to investigate Ca(2+)-mediated autophagy modulation. We imposed cellular stress by starvation or administration of etoposide (0.5-50 μM), sorafenib (1-40 μM), staurosporine (20-500 nM), or thapsigargin (20-500 nM) (1, 2, or 3 h) and measured the formation of WIPI-1 positive autophagosomal membranes. Automated analysis of up to 5000 individual cells/treatment demonstrated that Ca(2+) chelation by BAPTA-AM (10 and 30 μM) counteracted starvation or pharmacological compound-induced WIPI-1 puncta formation and LC3 lipidation. Application of selective Ca(2+)/calmodulin-dependent kinase kinase (CaMKK) α/β and calmodulin-dependent kinase (CaMK) I/II/IV inhibitors 7-oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic acid acetate (STO-609; 10-30 μg/ml) and 2-(N-[2-hydroxyethyl])-N-(4-methoxybenzenesulfonyl)amino-N-(4-chlorocinnamyl)-N-methylamine (KN-93; 1-10 μM), respectively, significantly reduced starvation-induced autophagosomal membrane formation, suggesting that Ca(2+) mobilization upon autophagy induction involves CaMKI/IV. By small interefering RNA (siRNA)-mediated down-regulation of CaMKI or CaMKIV, we demonstrate that CaMKI contributes to stimulation of WIPI-1. In line, WIPI-1 positive autophagosomal membranes were formed in AMP-activated protein kinase (AMPK) α(1)/α(2)-deficient mouse embryonic fibroblasts upon nutrient starvation, whereas basal autophagy was prominently reduced. However, transient down-regulation of AMPK by siRNA resulted in an increased basal level of both WIPI-1 puncta and LC3 lipidation, and nutrient-starvation induced autophagy was sensitive to STO-609/KN-93. Our data provide evidence that pharmacological compound-modulated and starvation-induced autophagy involves Ca(2+)-dependent signaling, including CaMKI independent of AMPKα(1)/α(2). Our data also suggest that AMPKα(1)/α(2) might differentially contribute to the regulation of WIPI-1 at the onset of autophagy.

摘要

自噬是由哺乳动物雷帕霉素靶蛋白(mTOR)抑制和磷脂酰肌醇 3-磷酸[PtdIns(3)P]生成引发的多膜囊泡(自噬体)形成所启动的。微管相关蛋白 1 轻链 3(LC3)上游,WD 重复蛋白与磷酸肌醇相互作用(WIPI 蛋白)特异性结合形成自噬体膜的 PtdIns(3)P,并成为生成的自噬体的膜结合蛋白。在这里,我们应用自动化高通量 WIPI-1 斑点分析,与 LC3 脂质化测定平行,研究 Ca(2+)介导的自噬调节。我们通过饥饿或依托泊苷(0.5-50 μM)、索拉非尼(1-40 μM)、星孢菌素(20-500 nM)或他泊昔琼(20-500 nM)(1、2 或 3 h)给药对细胞施加应激,并测量 WIPI-1 阳性自噬体膜的形成。高达 5000 个单个细胞/处理的自动分析表明,BAPTA-AM(10 和 30 μM)螯合 Ca(2+)可拮抗饥饿或药物化合物诱导的 WIPI-1 斑点形成和 LC3 脂质化。选择性 Ca(2+)/钙调蛋白依赖性激酶激酶(CaMKK)α/β和钙调蛋白依赖性激酶(CaMK)I/II/IV 抑制剂 7-氧代-7H-苯并咪唑[2,1-a]苯并[de]异喹啉-3-羧酸乙酸盐(STO-609;10-30 μg/ml)和 2-(N-[2-羟乙基])-N-(4-甲氧基苯磺酰基)氨基-N-(4-氯肉桂基)-N-甲基胺(KN-93;1-10 μM)的应用分别显著减少了饥饿诱导的自噬体膜形成,表明自噬诱导时的 Ca(2+)动员涉及 CaMKI/IV。通过小干扰 RNA(siRNA)介导的 CaMKI 或 CaMKIV 下调,我们证明 CaMKI 有助于 WIPI-1 的刺激。与此一致,在营养饥饿时,AMP 激活的蛋白激酶(AMPK)α(1)/α(2)缺陷型小鼠胚胎成纤维细胞中形成了 WIPI-1 阳性自噬体膜,而基础自噬明显减少。然而,siRNA 瞬时下调 AMPK 导致 WIPI-1 斑点和 LC3 脂质化的基础水平增加,并且 STO-609/KN-93 对营养饥饿诱导的自噬敏感。我们的数据提供了证据,表明药物化合物调节和饥饿诱导的自噬涉及 Ca(2+)依赖性信号传导,包括 AMPKα(1)/α(2)不依赖的 CaMKI。我们的数据还表明,AMPKα(1)/α(2)可能在自噬的起始时以不同的方式有助于 WIPI-1 的调节。

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