Burgoyne Joseph R, Eaton Philip
Cardiovascular Division, The Rayne Institute, St. Thomas' Hospital, King's College London, London SE17EH, United Kingdom.
J Biol Chem. 2009 Oct 23;284(43):29260-8. doi: 10.1074/jbc.M109.046722. Epub 2009 Sep 2.
The transnitrosylating nitric oxide (NO) donor nitrocysteine (CysNO) induced a disulfide bond between the two regulatory RI subunits of protein kinase A (PKA). The conventional NO donor S-nitroso-N-acetylpenicillamine failed to do this, consistent with our observation that it also did not promote protein S-nitrosylation. This disulfide oxidation event activated PKA and induced vasorelaxation independently of the classical beta-adrenergic or NO signaling pathway. Activation of PKA had also been anticipated to exert a positive inotropic effect on the myocardium but did not. The lack of positive inotropy was explained by CysNO concomitantly activating protein kinase G (PKG) Ialpha. PKG was found to exert a partial negative inotropic influence regardless of whether PKA was activated by classical beta-receptor stimulation or by disulfide bond formation. This work demonstrates that NO molecules that can induce S-nitrosylation directly activate type I PKA, providing a novel cross-talk to beta-adrenergic-like signaling without receptor or adenylate cyclase stimulation. However, the expected positive inotropic consequences of PKA activation by this novel mechanism are countermanded by the simultaneous dual activation of PKGIalpha, which is also activated by CysNO.
转亚硝基化一氧化氮(NO)供体硝巯基丙氨酸(CysNO)可诱导蛋白激酶A(PKA)的两个调节性RI亚基之间形成二硫键。传统的NO供体S-亚硝基-N-乙酰青霉胺则无法做到这一点,这与我们观察到它也不能促进蛋白质S-亚硝基化的结果一致。这种二硫键氧化事件激活了PKA,并独立于经典的β-肾上腺素能或NO信号通路诱导血管舒张。PKA的激活也曾被预期会对心肌产生正性肌力作用,但实际并非如此。缺乏正性肌力作用的原因是CysNO同时激活了蛋白激酶G(PKG)Iα。无论PKA是通过经典的β受体刺激还是通过二硫键形成而被激活,都发现PKG会产生部分负性肌力影响。这项研究表明,能够诱导S-亚硝基化的NO分子可直接激活I型PKA,在没有受体或腺苷酸环化酶刺激的情况下,与β-肾上腺素能样信号形成一种新的相互作用。然而,这种新机制激活PKA所预期的正性肌力作用被PKGIα的同时双重激活所抵消,PKGIα也可被CysNO激活。