College of Animal Science and Technology and.
College of Life Science and Food Engineering, Inner Mongolia University for Nationalities, Tong Liao, People's Republic of China.
J Dairy Res. 2020 Aug;87(3):344-348. doi: 10.1017/S0022029920000722. Epub 2020 Sep 7.
We determined the effects of a combination of C18 unsaturated fatty acids (C18-UFAs) consisting of oleic, linoleic, and linolenic acids on milk lipogenesis in bovine mammary epithelial cells (BMECs). By orthogonal experiments to determine cellular triacylglycerol (TAG) accumulation, a combination of 200 μmol/l C18 : 1, 50 μmol/l C18 : 2, and 2 μmol/l C18 : 3 was selected as C18-UFAs combination treatment, and culture in medium containing fatty acid-free bovine serum albumin was used as the control. The expression of genes related to milk lipid synthesis and intracellular FA composition was measured. The results showed that cytosolic TAG formation was higher under C18-UFAs treatment than under control treatment. The mRNA expression of acetyl-CoA carboxylase-α (ACACA), fatty acid synthase (FASN), and peroxisome proliferator-activated receptor gamma (PPARG) did not differ between treatments. The abundance of stearoyl-CoA desaturase (SCD) and acyl-CoA synthetase long-chain family member 1 (ACSL1) was higher, whereas that of sterol regulatory element binding transcription factor 1 (SREBF-1) was lower after C18-UFAs treatment compared to control treatment. The C16 : 0 and SFA content was decreased following C18-UFAs treatment compared to control treatment, while the cis-9 C18 : 1 and UFA content was increased. In conclusion, C18-UFAs could stimulate triglyceride accumulation, increase the cellular UFA concentration, and regulate lipogenic genes in BMECs.
我们研究了由油酸、亚油酸和亚麻酸组成的 C18 不饱和脂肪酸 (C18-UFAs) 混合物对牛乳腺上皮细胞 (BMECs) 中乳脂生成的影响。通过正交实验确定细胞三酰基甘油 (TAG) 积累,选择 200 μmol/l C18 : 1、50 μmol/l C18 : 2 和 2 μmol/l C18 : 3 的组合作为 C18-UFAs 组合处理,并用不含脂肪酸的牛血清白蛋白培养基培养作为对照。测量与乳脂合成和细胞内 FA 组成相关的基因表达。结果表明,C18-UFAs 处理下细胞质 TAG 形成高于对照处理。乙酰辅酶 A 羧化酶-α (ACACA)、脂肪酸合酶 (FASN) 和过氧化物酶体增殖物激活受体 γ (PPARG) 的 mRNA 表达在两种处理之间没有差异。硬脂酰辅酶 A 去饱和酶 (SCD) 和长链酰基辅酶 A 合成酶家族成员 1 (ACSL1) 的丰度较高,而固醇调节元件结合转录因子 1 (SREBF-1) 的丰度较低在 C18-UFAs 处理后比对照处理。与对照处理相比,C18-UFAs 处理后 C16 : 0 和 SFA 含量降低,而顺式 9 C18 : 1 和 UFA 含量增加。总之,C18-UFAs 可以刺激甘油三酯积累,增加细胞内 UFA 浓度,并调节 BMECs 中的脂肪生成基因。