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Changes in the asymmetric distribution of cholesterol in the plasma membrane influence streptolysin O pore formation

机译:质膜中胆固醇的不对称分布变化影响链球菌溶血素O孔的形成

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摘要

ATP-binding cassette A1 (ABCA1) plays a key role in generating high-density lipoprotein (HDL) and preventing atherosclerosis. ABCA1 exports cholesterol and phospholipid to apolipoprotein A-I (apoA-I) in serum to generate HDL. We found that streptolysin O (SLO), a cholesterol-dependent pore-forming toxin, barely formed pores in ABCA1-expressing cells, even in the absence of apoA-I. Neither cholesterol content in cell membranes nor the amount of SLO bound to cells was affected by ABCA1. On the other hand, binding of the D4 domain of perfringolysin O (PFO) to ABCA1-expressing cells increased, suggesting that the amount of cholesterol in the outer leaflet of the plasma membrane (PM) increased and that the cholesterol dependences of these two toxins differ. Addition of cholesterol to the PM by the MβCD–cholesterol complex dramatically restored SLO pore formation in ABCA1-expressing cells. Therefore, exogenous expression of ABCA1 causes reduction in the cholesterol level in the inner leaflet, thereby suppressing SLO pore formation.
机译:ATP结合盒A1(ABCA1)在产生高密度脂蛋白(HDL)和预防动脉粥样硬化中起关键作用。 ABCA1将胆固醇和磷脂输出到血清中的载脂蛋白A-I(apoA-I)中以产生HDL。我们发现,即使在没有apoA-I的情况下,链球菌溶血素O(SLO)(一种胆固醇依赖性成孔毒素)也几乎不会在表达ABCA1的细胞中形成孔。细胞膜中的胆固醇含量和与细胞结合的SLO量均不受ABCA1的影响。另一方面,产气荚膜溶素O(PFO)的D4结构域与表达ABCA1的细胞的结合增加,表明质膜(PM)外小叶中的胆固醇含量增加,并且这两种毒素的胆固醇依赖性不同。 MβCD-胆固醇复合物将胆固醇添加到PM中可显着恢复表达ABCA1的细胞中SLO孔的形成。因此,ABCA1的外源表达引起内部小叶中胆固醇水平的降低,从而抑制了SLO孔的形成。

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