Trøen G, Nilsson A, Norum K R, Blomhoff R
Institute for Nutrition Research, University of Oslo, Norway.
Biochem J. 1994 Jun 15;300 ( Pt 3)(Pt 3):793-8. doi: 10.1042/bj3000793.
The stellate cells of the liver are the main storage site of retinyl esters in the body. During cultivation in vitro of stellate cells isolated from rat and rabbit livers were observed that the cells rapidly loose their retinyl ester content. Freshly isolated stellate cells contain about 144 nmol of total retinol/mg of protein, while cells cultivated for 14 days contained below 0.1 nmol/mg of protein. When 3-day-old cultures were incubated for 6 h with 2 microM retinol, the cellular content increased from 5.6 to approx. 9.4 nmol of total retinyl esters/mg of protein. In contrast, little retinyl ester accumulated in 10-20-day-old cultures incubated with 2 microM retinol. At 50 microM retinol, however, the retinyl ester level did increase both with 3-day-old cultures and 10-20-day-old cultures. In parallel experiments with cultured fibroblasts esterification characteristics similar to those seen in older cultures of stellate cells were observed. When 10-day-old cultures of stellate cells were incubated with retinol alone, or in combination with palmitic acid, linoleic acid or oleic acid, the total storage of retinyl esters increased by 20-150%. In most cases, the fatty acid supplemented in the medium was found to be the dominant fatty acid esterified with retinol. Cultures of stellate cells were then exposed to a physiological concentration (1.3 microM) of radioactive retinol free in solution or bound to retinol-binding protein. With 3-day-old cultures, as well as older cultures, the cellular content of unesterified retinol was 10-20 times higher when free retinol was added compared with addition of retinol bound to retinol-binding protein. However, 2-3-fold as much radioactive retinyl esters were recovered in cells incubated with retinol-retinol-binding protein compared with retinol free in solution. These results show that retinol delivered to stellate cells from retinol-binding protein is preferentially esterified, and that the complex is handled differently to free retinol by the stellate cells.
肝脏星状细胞是体内视黄酯的主要储存部位。在体外培养从大鼠和兔肝脏分离的星状细胞时,观察到这些细胞会迅速失去其视黄酯含量。刚分离的星状细胞每毫克蛋白质含有约144 nmol的总视黄醇,而培养14天的细胞每毫克蛋白质所含低于0.1 nmol。当3日龄培养物与2 μM视黄醇孵育6小时时,细胞内视黄酯总量从5.6增加到约9.4 nmol/毫克蛋白质。相比之下,用2 μM视黄醇孵育10 - 20日龄培养物时,视黄酯积累较少。然而,在50 μM视黄醇时,3日龄培养物和10 - 20日龄培养物的视黄酯水平均有所增加。在与培养的成纤维细胞进行的平行实验中,观察到了与星状细胞较老培养物中相似的酯化特性。当10日龄的星状细胞培养物单独与视黄醇孵育,或与棕榈酸、亚油酸或油酸联合孵育时,视黄酯的总储存量增加了20% - 150%。在大多数情况下,培养基中添加的脂肪酸被发现是与视黄醇酯化的主要脂肪酸。然后将星状细胞培养物暴露于生理浓度(1.3 μM)的游离放射性视黄醇或与视黄醇结合蛋白结合的视黄醇中。对于3日龄培养物以及较老的培养物,添加游离视黄醇时未酯化视黄醇的细胞含量比添加与视黄醇结合蛋白结合的视黄醇时高10 - 20倍。然而,与游离视黄醇相比,用视黄醇 - 视黄醇结合蛋白孵育的细胞中回收的放射性视黄酯多2 - 3倍。这些结果表明,从视黄醇结合蛋白传递给星状细胞的视黄醇优先被酯化,并且星状细胞对该复合物的处理方式与游离视黄醇不同。