Kwekkeboom J, van Voorthuizen E M, Princen H M, Kempen H J
Gaubius Institute TNO, Leiden, The Netherlands.
Biochem Biophys Res Commun. 1988 Sep 15;155(2):850-6. doi: 10.1016/s0006-291x(88)80573-4.
Bile acid synthesis by cultured pig hepatocytes, as measured by conversion of [14C]cholesterol to bile acids, increased during the second and third day of culture. This rise was inhibited after addition of various conjugated and unconjugated bile acids in a concentration of 100 microM. It could be completely prevented by cycloheximide, indicating that de novo protein synthesis is required for the increase in bile acid formation. No effect of exogenous bile salts on LDH release to the medium or on cellular ATP content was observed, demonstrating that hepatocyte viability was not affected. During the period in which bile acid synthesis was inhibited, pig hepatocytes were able to accumulate taurocholic acid (100 microM) up to 7-18 nmol per mg cell protein (decreasing during culture time). It is concluded that feedback regulation of bile acid synthesis is exerted by direct action of bile acids on the hepatocyte.
通过[14C]胆固醇转化为胆汁酸来测定,培养的猪肝细胞的胆汁酸合成在培养的第二天和第三天增加。在添加浓度为100微摩尔的各种结合型和非结合型胆汁酸后,这种增加受到抑制。放线菌酮可以完全阻止这种增加,这表明胆汁酸形成增加需要从头合成蛋白质。未观察到外源性胆盐对培养基中乳酸脱氢酶释放或细胞ATP含量有影响,这表明肝细胞活力未受影响。在胆汁酸合成受到抑制的期间,猪肝细胞能够积累牛磺胆酸(100微摩尔),达到每毫克细胞蛋白7 - 18纳摩尔(在培养期间减少)。结论是胆汁酸对肝细胞的直接作用发挥了胆汁酸合成的反馈调节作用。