Maehara K
Department of Laboratory Medicine, Faculty of Medicine, Kagoshima University.
Fukuoka Igaku Zasshi. 1991 Nov;82(11):586-602.
The author studied influence of membrane cholesterol on insulin receptor behavior using human erythrocytes after modification of their membrane cholesterol contents. Insulin binding to the erythrocytes containing higher membrane cholesterol which were obtained from alcoholic liver cirrhosis (ALC) and familial lecithin: cholesterol acyl transferase (LCAT) deficiency patients was also examined. 1) Influence of modified membrane cholesterol contents on insulin binding to erythrocytes (in vitro experiments): The cholesterol content of human erythrocyte membranes was modified by incubating the cells with phosphatidylcholine/cholesterol and phosphatidylcholine vesicles. Then insulin binding to the erythrocytes was measured as a function of membrane cholesterol content. Low membrane cholesterol decreased insulin binding at 10 degrees C and 15 degrees C, but increased insulin binding at 25 degrees C and 37 degrees C. Scatchard plot analysis showed that low membrane cholesterol decreased a number of the receptor without alteration of affinity. Phosphatidylcholine spin probe showed a dual effect of cholesterol on membrane fluidity, fluidizing below but rigidifying membranes above 20 degrees C. It is suggested that membrane cholesterol affects insulin receptor behavior through alteration of membrane fluidity, depending on the phase state of the membranes. 2) Insulin binding and membrane lipid composition of erythrocytes from ALC and LCAT deficiency patients: The erythrocytes from both ALC and LCAT deficiency patients are known to have higher content of membrane cholesterol. Insulin binding and membrane lipid composition of erythrocytes in both diseases were measured to see the influence of cholesterol on insulin binding in sites. a) Erythrocytes from ALC patients: In the erythrocytes from ALC patients, cholesterol to phospholipid molar ratio was significantly increased as compared with normal subjects. In phospholipid acyl chains, contents of polyunsaturated fatty acid significantly decreased in ALC patients. Insulin binding to erythrocytes was significantly increased in the patients of ALC. Scatchard plot analysis (at 15 degrees C) showed significant increase of the receptor number in erythrocytes from the ALC patients as compared to the normal subjects, while the affinity did not differ between the groups. The increased cholesterol content in the erythrocyte membranes was suggested to be responsible for the increased receptor number and insulin binding to the erythrocytes from ALC patients. b) Erythrocytes from LCAT deficiency patients: Membrane cholesterol to phospholipid molar ratio was increased in two patients of LCAT deficiency studied. In phospholipid classes, increase of phosphatidylcholine and decreases of both phosphatidylethanolamine and sphingomyelin were observed in the erythrocytes from both patients.(ABSTRACT TRUNCATED AT 400 WORDS)
作者通过改变人红细胞膜胆固醇含量,研究了膜胆固醇对胰岛素受体行为的影响。还检测了胰岛素与酒精性肝硬化(ALC)患者及家族性卵磷脂胆固醇酰基转移酶(LCAT)缺乏症患者来源的、膜胆固醇含量较高的红细胞的结合情况。1)改变膜胆固醇含量对胰岛素与红细胞结合的影响(体外实验):通过将细胞与磷脂酰胆碱/胆固醇和磷脂酰胆碱囊泡孵育,改变人红细胞膜的胆固醇含量。然后测定胰岛素与红细胞的结合情况,并将其作为膜胆固醇含量的函数。低膜胆固醇在10℃和15℃时降低胰岛素结合,但在25℃和37℃时增加胰岛素结合。Scatchard图分析表明,低膜胆固醇减少了受体数量,但亲和力未改变。磷脂酰胆碱自旋探针显示胆固醇对膜流动性有双重作用,在20℃以下使膜流化,在20℃以上使膜硬化。提示膜胆固醇通过改变膜流动性影响胰岛素受体行为,这取决于膜的相态。2)ALC和LCAT缺乏症患者红细胞的胰岛素结合及膜脂质组成:已知ALC和LCAT缺乏症患者的红细胞膜胆固醇含量较高。检测了这两种疾病患者红细胞的胰岛素结合及膜脂质组成,以观察胆固醇对胰岛素结合位点的影响。a)ALC患者的红细胞:与正常受试者相比,ALC患者红细胞中胆固醇与磷脂的摩尔比显著增加。在磷脂酰链中,ALC患者多不饱和脂肪酸含量显著降低。ALC患者红细胞与胰岛素的结合显著增加。Scatchard图分析(在15℃时)显示,与正常受试者相比,ALC患者红细胞中的受体数量显著增加,而两组之间的亲和力无差异。红细胞膜中胆固醇含量增加被认为是ALC患者红细胞受体数量增加及胰岛素结合增加的原因。b)LCAT缺乏症患者的红细胞:在所研究的两名LCAT缺乏症患者中,膜胆固醇与磷脂的摩尔比增加。在磷脂类中,两名患者的红细胞中磷脂酰胆碱增加,磷脂酰乙醇胺和鞘磷脂均减少。(摘要截断于400字)