Division of Clinical Nutrition, Department of Nutritional Science, Sagami Womens University, 211 Bunkyo, Sagamihara, Kanagawa 2288533, Japan.
Cell Biol Int. 2011 Jan;35(1):51-9. doi: 10.1042/CBI20100070.
We examined the effect of n-3 PUFAs (polyunsaturated fatty acids) on the growth and maturation of human preadipocyte cell line AML-I. On day 3 of the culture, n-3 fatty acids such as DHA (docosahexaenoic acid) and EPA (eicosapentaenoic acid), but not n-6 fatty acid LA (linoleic acid), induced growth arrest accompanied by the appearance of characteristics of apoptosis in AML-I cells at concentrations between 250 and 500 μM by Annexin V-FITC staining. In Western blotting analysis, the loss of NF-κB, Bcl-2 and p-Akt and the accumulation of Bad and Akt were observed in the cytoplasmic protein from the EPA-treated cells. Exposure of AML-I to EPA or DHA increased the cytoplasmic lipid accumulation compared with the vehicle-treated cells in a time-dependent manner during 4 and 6 days culture period by Oil Red O staining. The expression of FAS (fatty acid synthase) and PPAR-γ (peroxisome proliferator-activated receptor-γ) were increased in EPA-treated cells. These results suggest that EPA and DHA promote differentiation, inhibit proliferation and induce apoptosis in preadipocyte cell line AML-I.
我们研究了 n-3 多不饱和脂肪酸(PUFAs)对人前体脂肪细胞系 AML-I 生长和成熟的影响。在培养的第 3 天,n-3 脂肪酸如 DHA(二十二碳六烯酸)和 EPA(二十碳五烯酸),但不是 n-6 脂肪酸 LA(亚油酸),在 250 和 500 μM 浓度下通过 Annexin V-FITC 染色诱导 AML-I 细胞生长停滞,并伴有凋亡特征的出现。在 Western blotting 分析中,从 EPA 处理的细胞的细胞质蛋白中观察到 NF-κB、Bcl-2 和 p-Akt 的丢失以及 Bad 和 Akt 的积累。用油红 O 染色法在 4 和 6 天培养期间,与载体处理的细胞相比,EPA 或 DHA 处理的 AML-I 细胞中细胞质脂质积累呈时间依赖性增加。EPA 处理的细胞中 FAS(脂肪酸合酶)和 PPAR-γ(过氧化物酶体增殖物激活受体-γ)的表达增加。这些结果表明,EPA 和 DHA 可促进前体脂肪细胞系 AML-I 的分化、抑制增殖并诱导凋亡。