Jibril N, Mori Y, Tanaka Y, Sakata T, Miki H, Sakakibara T, Sato M, Hayashi S
Laboratory of Food Chemistry, Faculty of Fisheries, Kagoshima University, Japan.
Cell Struct Funct. 1995 Oct;20(5):301-10. doi: 10.1247/csf.20.301.
Specific binding of eel serum high-density lipoprotein (HDL) to eel hepatocytes was demonstrated by using a synthesized fluorescent lipophilic dye. HDL binding was inhibited by the addition of unlabeled HDL. The binding of HDL to the hepatocytes was saturated at concentrations over 100 micrograms HDL protein/ml and Kd value was 20 micrograms HDL protein/ml. A fluorescent photomicrograph of the cultured eel hepatocytes which were incubated with the dye showed the bright, circumferential plasma membranes stained with the dye. 125I-HDL was incorporated into the acid insoluble- and soluble-fractions of the cultured hepatocytes during incubation at 28 degrees C for 1 h. There are three remarkable characteristics of the effect of HDL on the cultured hepatocytes. One is that the addition of HDL to the hepatocytes induced the efflux of cholesterol, triacylglycerol, and phospholipid from the hepatocytes. The second characteristic is that the efflux of the intracellular lipids was carried out with very-low-density-like or chylomicron-like lipoprotein secreted by the hepatocytes. The third characteristic is that HDL specifically stimulated the synthesis of the lipoprotein and had no effect on the synthesis of intracellular proteins and the secreted proteins except for the lipoprotein.
通过使用合成的荧光亲脂性染料,证明了鳗鱼血清高密度脂蛋白(HDL)与鳗鱼肝细胞的特异性结合。未标记的HDL的添加抑制了HDL的结合。HDL与肝细胞的结合在HDL蛋白浓度超过100微克/毫升时达到饱和,Kd值为20微克HDL蛋白/毫升。用该染料孵育的培养鳗鱼肝细胞的荧光显微照片显示,明亮的外周质膜被该染料染色。在28℃孵育1小时期间,125I-HDL被掺入培养肝细胞的酸不溶性和可溶性部分。HDL对培养肝细胞的作用有三个显著特征。一是向肝细胞中添加HDL会诱导胆固醇、三酰甘油和磷脂从肝细胞中流出。第二个特征是细胞内脂质的流出是由肝细胞分泌的极低密度脂蛋白样或乳糜微粒样脂蛋白进行的。第三个特征是HDL特异性刺激脂蛋白的合成,对细胞内蛋白质和除脂蛋白外的分泌蛋白的合成没有影响。