Kasina S, Wasia R, Fasim Aneesa, Radhika K V N, Singh Surya S
Department of Biochemistry, Osmania University, Hyderabad, India [corrected]
Nitric Oxide. 2006 Feb;14(1):65-71. doi: 10.1016/j.niox.2005.09.008. Epub 2005 Nov 8.
Nitric oxide is an important precursor for peroxynitrite production under in vivo conditions leading to cell injury and cell death. In platelets, a number of cytosolic and actin binding proteins were shown to be nitrated [K.M. Naseem, S.Y. Low, M. Sabetkar, N.J. Bradley, J. Khan, M. Jacobs, K.R. Bruckdorfer, The nitration of platelet cytosolic proteins during agonist-induced activation of platelets. FEBS Lett. 473 (1) (2000) 199-122 and M. Sabetkar, S.Y. Low, K.M. Naseem, K.R. Bruckdorfer, The nitration of proteins in platelets: significance in platelet function, Free Radic. Biol. Med. 33 (6) (2002) 728-736]. We investigated the possible mechanism that regulates profilin (an actin binding protein) nitration in platelets. Activation of bovine platelets with arachidonic acid, thrombin, and phorbol 12,13-dibutyrate resulted in nitration of profilin on tyrosine residue. In vivo profilin nitration showed a four- and eight-fold increase in the presence of thrombin and phorbol 12,13-dibutyrate, respectively. Analysis of nitroprofilin levels in the presence of NOS inhibitors (1400W and EGTA), indicated that profilin nitration in phorbol 12,13-dibutyrate treated platelets is mediated by inducible nitric oxide synthase. Phorbol ester treated platelets exhibited higher levels by inducible nitric oxide synthase (491% over control), while total nitric oxide synthase activity increased by 5% over control. Higher levels of peroxynitrite in platelets treated with phorbol 12,13-dibutyrate indicated that profilin nitration is mediated by peroxynitrite. Increase in phosphatidylinositol 3-kinase (PI 3-kinase) activity in platelets treated with thrombin and phorbol 12,13-dibutyrate indicates that nitration of platelet profilin could be mediated by PI 3-kinase. A decrease in the level of nitroprofilin in PDBu treated platelets in the presence of inducible nitric oxide synthase inhibitor, 1400W, was observed suggesting that profilin nitration is mediated by PI 3-kinase dependent activation of inducible nitric oxide synthase.
在体内条件下,一氧化氮是过氧亚硝酸盐生成的重要前体,会导致细胞损伤和细胞死亡。在血小板中,许多胞质和肌动蛋白结合蛋白被证明发生了硝化作用[K.M.纳塞姆、S.Y.洛、M.萨贝卡尔、N.J.布拉德利、J.汗、M.雅各布斯、K.R.布鲁克多弗,激动剂诱导血小板活化过程中血小板胞质蛋白的硝化作用。《欧洲生物化学学会联合会快报》473 (1) (2000) 199 - 122以及M.萨贝卡尔、S.Y.洛、K.M.纳塞姆、K.R.布鲁克多弗,血小板中蛋白质的硝化作用:对血小板功能的意义,《自由基生物学与医学》33 (6) (2002) 728 - 736]。我们研究了调节血小板中肌动蛋白结合蛋白(即丝切蛋白)硝化作用的可能机制。用花生四烯酸、凝血酶和佛波醇12,13 - 二丁酸激活牛血小板会导致丝切蛋白酪氨酸残基发生硝化作用。在体内,分别在存在凝血酶和佛波醇12,13 - 二丁酸的情况下,丝切蛋白硝化作用增加了四倍和八倍。在一氧化氮合酶抑制剂(1400W和乙二醇双四乙酸)存在的情况下对硝基丝切蛋白水平进行分析,结果表明佛波醇12,13 - 二丁酸处理的血小板中丝切蛋白的硝化作用是由诱导型一氧化氮合酶介导的。佛波醇酯处理的血小板中诱导型一氧化氮合酶水平较高(比对照高491%),而总一氧化氮合酶活性比对照增加了5%。用佛波醇12,