Zhou Jiming, Ryan Alan J, Medh Jheem, Mallampalli Rama K
Department of Internal Medicine, The University of Iowa College of Medicine, Iowa City, Iowa 52242, USA.
J Biol Chem. 2003 Sep 26;278(39):37032-40. doi: 10.1074/jbc.M304316200. Epub 2003 Jul 11.
We investigated effects of pro-atherogenic oxidized lipoproteins on phosphatidylcholine (PtdCho) biosynthesis in murine lung epithelial cells (MLE-12). Cells surface-bound, internalized, and degraded oxidized low density lipoproteins (Ox-LDL). Ox-LDL significantly reduced [3H]choline incorporation into PtdCho in cells by selectively inhibiting the activity of the rate-regulatory enzyme, CTP:phosphocholine cytdylyltransferase (CCT). Ox-LDL coordinately increased the cellular turnover of CCTalpha protein as determined by [35S]methionine pulse-chase studies by inducing the calcium-activated proteinase, calpain. Forced expression of calpain or exposure of cells to the calcium ionophore, A23187, increased CCTalpha degradation, whereas overexpression of the endogenous calpain inhibitor, calpastatin, attenuated Ox-LDL-induced CCTalpha degradation. The effects of Ox-LDL on CCTalpha breakdown were attenuated in calpain-deficient cells. In vitro calpain digestion of CCTalpha isolated from cells transfected with truncated or internal deletion mutants indicated multiple cleavage sites within the CCTalpha primary structure, leading to the generation of a 26-kDa (p26) fragment. Calpain hydrolysis of purified CCTalpha generated p26, which upon NH2-terminal sequencing localized a calpain attack site within the CCTalpha amino terminus. Expression of a CCTalpha mutant where the amino-terminal cleavage site and a putative carboxyl-terminal hydrolysis region were modified resulted in an enzyme that was significantly less sensitive to proteolytic cleavage and restored the ability of cells to synthesize surfactant PtdCho after Ox-LDL treatment. Thus, these results provide a critical link between proatherogenic lipoproteins and their metabolic target, CCTalpha, resulting in impaired surfactant metabolism.
我们研究了促动脉粥样硬化的氧化脂蛋白对小鼠肺上皮细胞(MLE-12)中磷脂酰胆碱(PtdCho)生物合成的影响。细胞可表面结合、内化并降解氧化低密度脂蛋白(Ox-LDL)。Ox-LDL通过选择性抑制限速酶CTP:磷酸胆碱胞苷转移酶(CCT)的活性,显著降低细胞中[3H]胆碱掺入PtdCho的水平。通过[35S]甲硫氨酸脉冲追踪研究确定,Ox-LDL通过诱导钙激活蛋白酶钙蛋白酶,协同增加CCTα蛋白的细胞周转率。强制表达钙蛋白酶或使细胞暴露于钙离子载体A23187会增加CCTα的降解,而内源性钙蛋白酶抑制剂钙蛋白酶抑制素的过表达则会减弱Ox-LDL诱导的CCTα降解。在缺乏钙蛋白酶的细胞中,Ox-LDL对CCTα分解的影响减弱。用截短或内部缺失突变体转染的细胞中分离出的CCTα进行体外钙蛋白酶消化,表明CCTα一级结构内有多个切割位点,导致产生一个26 kDa(p26)片段。纯化的CCTα经钙蛋白酶水解产生p26,通过NH2末端测序确定了CCTα氨基末端的钙蛋白酶攻击位点。对氨基末端切割位点和假定的羧基末端水解区域进行修饰的CCTα突变体的表达产生了一种对蛋白水解切割明显不敏感的酶,并恢复了Ox-LDL处理后细胞合成表面活性剂PtdCho的能力。因此,这些结果在促动脉粥样硬化脂蛋白与其代谢靶点CCTα之间提供了关键联系,导致表面活性剂代谢受损。