Lin R C
Biochim Biophys Acta. 1984 Apr 18;793(2):193-201. doi: 10.1016/0005-2760(84)90321-7.
We used monolayer cultured rat hepatocytes as an experimental model to study the secretion of the newly synthesized cholesterol by the liver. Cellular cholesterol was labeled by exposing cultured hepatocytes to [14C]acetate prior to the study of secretion. Secretion of the newly synthesized cholesterol was measured by extracting cholesterol in the culture medium and assaying for the radioactivity of [14C]cholesterol. We found that: (a) cultured hepatocytes could secrete newly synthesized cholesterol in serum-free medium; (b) secreted [14C]cholesterol was bound to macromolecule(s) and the secretion rate was not affected by cycloheximide for up to 5 h; (c) serum added to the culture medium greatly enhanced hepatic cholesterol secretion; (d) serum high-density lipoproteins were most effective, lipoprotein-deficient serum (d greater than 1.21) less effective in stimulating cholesterol secretion, whereas low-density and very-low-density lipoproteins had little effect; (e) when the serum-free culture medium was fractionated by ultracentrifugation, a major portion of the secreted [14C]cholesterol was found in the high-density lipoprotein fraction; (f) part of the medium [14C]cholesterol also turned up in the high-density lipoprotein fraction when lipoprotein-deficient serum was added as the acceptor; (g) secreted [14C]cholesterol was found only in free form, although some of the cellular [14C]cholesterol was found as esters.
我们使用单层培养的大鼠肝细胞作为实验模型,来研究肝脏新合成胆固醇的分泌情况。在研究分泌之前,通过将培养的肝细胞暴露于[14C]乙酸盐来标记细胞胆固醇。通过提取培养基中的胆固醇并检测[14C]胆固醇的放射性,来测量新合成胆固醇的分泌量。我们发现:(a)培养的肝细胞能够在无血清培养基中分泌新合成的胆固醇;(b)分泌的[14C]胆固醇与大分子结合,并且在长达5小时内,分泌速率不受环己酰亚胺的影响;(c)添加到培养基中的血清极大地增强了肝脏胆固醇的分泌;(d)血清高密度脂蛋白最有效,缺乏脂蛋白的血清(d大于1.21)刺激胆固醇分泌的效果较差,而低密度脂蛋白和极低密度脂蛋白几乎没有作用;(e)当通过超速离心对无血清培养基进行分级分离时,发现大部分分泌的[14C]胆固醇存在于高密度脂蛋白部分;(f)当添加缺乏脂蛋白的血清作为受体时,培养基中的部分[14C]胆固醇也出现在高密度脂蛋白部分;(g)分泌的[14C]胆固醇仅以游离形式存在,尽管部分细胞内的[14C]胆固醇以酯的形式存在。