Assmann G, Smootz E, Adler K, Capurso A, Oette K
J Clin Invest. 1977 Mar;59(3):565-75. doi: 10.1172/JCI108672.
In this study we have determined by radioimmunoassay and double immunoelectrophoresis the total quantities and distributions of A apoproteins in three adult patients affected with Tangier disease (hereditary alpha-lipoprotein deficiency). Compared with normal plasma, the total quantities of apoproteins A-I and A-II in Tangier plasma were determined to be less than 1% and 5-7%, respectively. In Tangier patients, approximately 90% of the apoprotein A-I sedimented when ultracentrifugations of plasma were carried out at density 1.21 g/ml KBr. By contrast, more than 95% of the apoprotein A-II floated under those conditions. In normal plasma, approximately 90% of both apoproteins A-I and A-II is found in the 1.063-1.21-g/ml KBr density fraction. These findings suggest that complete dissociation of A apoproteins occurs in Tangier plasma. This dissociation of apoproteins was confirmed by double immunoelectrophoresis with monospecific antisera. Immunochemical and electrophoretic experiments did not provide evidence for a structural abnormality of apoprotein A-I in these patients, The results taken together strongly suggest that normal high-density lipoproteins are absent from Tangier plasma.
在本研究中,我们通过放射免疫测定法和双向免疫电泳法,测定了三名患有Tangier病(遗传性α脂蛋白缺乏症)的成年患者中A载脂蛋白的总量及其分布情况。与正常血浆相比,Tangier血浆中载脂蛋白A-I和A-II的总量分别被测定为低于1%和5 - 7%。在Tangier病患者中,当血浆在密度为1.21 g/ml KBr条件下进行超速离心时,约90%的载脂蛋白A-I发生沉淀。相比之下,在这些条件下,超过95%的载脂蛋白A-II上浮。在正常血浆中,约90%的载脂蛋白A-I和A-II存在于密度为1.063 - 1.21 g/ml KBr的组分中。这些发现表明,Tangier血浆中A载脂蛋白发生了完全解离。用单特异性抗血清进行的双向免疫电泳证实了载脂蛋白的这种解离。免疫化学和电泳实验未提供证据表明这些患者的载脂蛋白A-I存在结构异常。综合这些结果强烈表明,Tangier血浆中不存在正常的高密度脂蛋白。