Lee M H, Lu K, Hazard S, Yu H, Shulenin S, Hidaka H, Kojima H, Allikmets R, Sakuma N, Pegoraro R, Srivastava A K, Salen G, Dean M, Patel S B
Division of Endocrinology, Diabetes and Medical Genetics, Medical University of South Carolina, Charleston, South Carolina, USA.
Nat Genet. 2001 Jan;27(1):79-83. doi: 10.1038/83799.
The molecular mechanisms regulating the amount of dietary cholesterol retained in the body, as well as the body's ability to exclude selectively other dietary sterols, are poorly understood. An average western diet will contain about 250-500 mg of dietary cholesterol and about 200-400 mg of non-cholesterol sterols. About 50-60% of the dietary cholesterol is absorbed and retained by the normal human body, but less than 1% of the non-cholesterol sterols are retained. Thus, there exists a subtle mechanism that allows the body to distinguish between cholesterol and non-cholesterol sterols. In sitosterolemia, a rare autosomal recessive disorder, affected individuals hyperabsorb not only cholesterol but also all other sterols, including plant and shellfish sterols from the intestine. The major plant sterol species is sitosterol; hence the name of the disorder. Consequently, patients with this disease have very high levels of plant sterols in the plasma and develop tendon and tuberous xanthomas, accelerated atherosclerosis, and premature coronary artery disease. We previously mapped the STSL locus to human chromosome 2p21 and further localized it to a region of less than 2 cM bounded by markers D2S2294 and D2S2291 (M.-H.L. et al., manuscript submitted). We now report that a new member of the ABC transporter family, ABCG5, is mutant in nine unrelated sitosterolemia patients.
调节体内膳食胆固醇留存量以及机体选择性排除其他膳食固醇的分子机制,目前仍知之甚少。典型的西方饮食中约含250 - 500毫克膳食胆固醇以及约200 - 400毫克非胆固醇固醇。正常人体会吸收并留存约50 - 60%的膳食胆固醇,但留存的非胆固醇固醇不到1%。因此,机体存在一种微妙的机制,能够区分胆固醇和非胆固醇固醇。在谷甾醇血症(一种罕见的常染色体隐性疾病)中,患病个体不仅会过度吸收胆固醇,还会从肠道过度吸收包括植物和贝类固醇在内的所有其他固醇。主要的植物固醇种类是谷甾醇,因此该疾病以此命名。所以,患有这种疾病的患者血浆中植物固醇水平非常高,并会出现肌腱和结节性黄瘤、动脉粥样硬化加速以及早发性冠状动脉疾病。我们之前已将STSL基因座定位到人类染色体2p21,并进一步将其定位到由标记D2S2294和D2S2291界定的小于2厘摩的区域(M.-H.L.等人,已提交论文)。我们现在报告,ABC转运蛋白家族的一个新成员ABCG5,在9名无亲缘关系的谷甾醇血症患者中发生了突变。