Serdyuk A P, Morton R E
Department of Cell Biology, The Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):718-26. doi: 10.1161/01.atv.19.3.718.
Cholesteryl ester transfer protein (CETP) catalyzes the net transfer of cholesteryl ester (CE) between lipoproteins in exchange for triglyceride (heteroexchange). It is generally held that CETP primarily associates with HDL and preferentially transfers lipids from this lipoprotein fraction. This is illustrated in normal plasma where HDL is the primary donor of the CE transferred to VLDL by CETP. However, in plasma deficient in lipid transfer inhibitor protein (LTIP) activity, HDL and LDL are equivalent donors of CE to VLDL (Arterioscler Thromb Vasc Biol. 1997;17:1716-1724). Thus, we have hypothesized that the preferential transfer of CE from HDL in normal plasma is a consequence of LTIP activity and not caused by a preferential CETP-HDL interaction. We have tested this hypothesis in lipid mass transfer assays with partially purified CETP and LTIP, and isolated lipoproteins. With a physiological mixture of lipoproteins, the preference ratio (PR, ratio of CE mass transferred from a lipoprotein to VLDL versus its CE content) for HDL and LDL in the presence of CETP alone was approximately 1 (ie, no preference). Fourfold variations in the LDL/HDL ratio or in the levels of HDL in the assay did not result in significant preferential transfer from any lipoprotein. On addition of LTIP, the PR for HDL was increased up to 2-fold and that for LDL decreased in a concentration-dependent manner. Under all conditions where LDL and HDL levels were varied, LTIP consistently resulted in a PR >1 for CE transfer from HDL. Short-term experiments with radiolabeled lipoproteins and either partially purified or homogenous CETP confirmed these observations and further demonstrated that CETP has a strong predilection to mediate homoexchange (bidirectional transfer of the same lipid) rather than heteroexchange (CE for TG); LTIP had no effect on the selection of CE or TG by CETP or its mechanism of action. We conclude, in contrast to current opinion, that CETP has no preference for CE in HDL versus LDL, suggesting that the previously reported stable binding of CETP to HDL does not result in selective transfer from this lipoprotein. These data suggest that LTIP is responsible for the preferential transfer of CE from HDL that occurs in plasma. CETP and LTIP cooperatively determine the extent of CETP-mediated remodeling of individual lipoprotein fractions.
胆固醇酯转运蛋白(CETP)催化脂蛋白之间胆固醇酯(CE)与甘油三酯的净交换(异质交换)。一般认为,CETP主要与高密度脂蛋白(HDL)结合,并优先从该脂蛋白组分转运脂质。正常血浆中就体现了这一点,其中HDL是CETP将CE转运至极低密度脂蛋白(VLDL)的主要供体。然而,在缺乏脂质转运抑制蛋白(LTIP)活性的血浆中,HDL和低密度脂蛋白(LDL)作为CE至VLDL的供体是等效的(《动脉硬化血栓与血管生物学》。1997年;17:1716 - 1724)。因此,我们推测正常血浆中HDL优先转运CE是LTIP活性的结果,而非CETP与HDL之间优先相互作用所致。我们在脂质质量转移试验中使用部分纯化的CETP和LTIP以及分离的脂蛋白对这一假设进行了验证。在脂蛋白的生理混合物中,仅存在CETP时,HDL和LDL的优先比率(PR,从脂蛋白转运至VLDL的CE质量与其CE含量之比)约为1(即无优先性)。试验中LDL/HDL比率或HDL水平的四倍变化并未导致从任何脂蛋白的显著优先转运。加入LTIP后,HDL的PR增加至2倍,而LDL的PR则以浓度依赖方式降低。在LDL和HDL水平变化的所有条件下,LTIP始终导致从HDL转运CE的PR>1。用放射性标记脂蛋白以及部分纯化或均质的CETP进行的短期实验证实了这些观察结果,并进一步表明CETP强烈倾向于介导同质交换(相同脂质的双向转运)而非异质交换(CE换TG);LTIP对CETP选择CE或TG及其作用机制没有影响。与当前观点相反,我们得出结论,CETP对HDL中的CE与LDL中的CE并无偏好,这表明先前报道的CETP与HDL的稳定结合并不会导致从该脂蛋白的选择性转运。这些数据表明,LTIP负责血浆中发生的HDL优先转运CE。CETP和LTIP共同决定了CETP介导的各个脂蛋白组分重塑的程度。