Hsu J M, Ding S T
Department of Animal Science, National Taiwan University, Taipei 106, Taiwan.
Br J Nutr. 2003 Sep;90(3):507-13. doi: 10.1079/bjn2003918.
Polyunsaturated fatty acids (FA) regulate genes involved in lipid metabolism. The effects of polyunsaturated FA on the transcription factor adipocyte determination and differentiation-dependent factor (ADD) 1 and fatty acid synthase (FAS) mRNA in differentiating porcine adipocytes were measured using a stromal vascular cell culture system. Porcine stromal vascular cells were isolated from subcutaneous adipose tissues and plated in Dulbecco's modified Eagle's medium (DMEM)-nutrient mixture F-12 Ham (F-12) plus fetal bovine serum (100 ml/l) for 24 h. Then cells were differentiated in DMEM-F12 plus insulin, hydrocortisone and transferrin without or with polyunsaturated FA at 6.25, 25.00 or 100.00 microM. The ADD1 mRNA was decreased by 100.00 microM-arachidonic acid, 6.25 to 100.00 microM-docosahexaenoic acid or cis-9,trans-11-conjugated linoleic acid. The polyunsaturated FA reduced the transcription rate of FAS, but not of ADD1. All three polyunsaturated FA accelerated degradation of ADD1 and FAS mRNA to reduce the abundance of ADD1 and FAS mRNA. Results also showed that polyunsaturated FA inhibit the ADD1 expression, not only of mRNA concentration, but also of mature ADD1 protein concentration, suggesting an overall reduction of ADD1 function by polyunsaturated FA. Our present experiments demonstrate that polyunsaturated FA regulate the gene expression of ADD1 and enzymes involved in lipid metabolism in porcine adipocytes.
多不饱和脂肪酸(FA)可调节参与脂质代谢的基因。利用基质血管细胞培养系统,检测了多不饱和脂肪酸对分化中的猪脂肪细胞中转录因子脂肪细胞决定和分化依赖因子(ADD)1以及脂肪酸合酶(FAS)mRNA的影响。从皮下脂肪组织中分离出猪基质血管细胞,接种于含有100 ml/l胎牛血清的杜氏改良 Eagle 培养基(DMEM)-营养混合物F-12 Ham(F-12)中培养24小时。然后,将细胞在含有或不含有6.25、25.00或100.00微摩尔多不饱和脂肪酸的DMEM-F12加胰岛素、氢化可的松和转铁蛋白的培养基中进行分化。100.00微摩尔花生四烯酸、6.25至100.00微摩尔二十二碳六烯酸或顺-9,反-11-共轭亚油酸可使ADD1 mRNA水平降低。多不饱和脂肪酸降低了FAS的转录速率,但对ADD1的转录速率没有影响。这三种多不饱和脂肪酸均加速了ADD1和FAS mRNA的降解,从而降低了ADD1和FAS mRNA水平。结果还表明,多不饱和脂肪酸不仅抑制ADD1 mRNA浓度,还抑制成熟ADD1蛋白浓度,提示多不饱和脂肪酸可全面降低ADD1功能。我们目前的实验表明,多不饱和脂肪酸可调节猪脂肪细胞中ADD1的基因表达以及参与脂质代谢的酶的表达。