Department of Food Science and Engineering, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, 150001, P. R. China.
Key Laboratory of Shandong Provincial Education Department: Past-harvest QC and Multiutilization of Characteristic Agricultural Products, Shandong Agriculture and Food Engineering University, Jinan, Shandong, 250100, P. R. China.
Sci Rep. 2019 Feb 22;9(1):2577. doi: 10.1038/s41598-019-39546-y.
Bovine milk fat globule membrane (MFGM) has shown many health benefits, however, there has not been much study on non-cattle MFGMs. The purpose of this study was to compare the anti-proliferation effects and investigate the mechanisms of MFGMs from bovine, goat, buffalo, yak and camel milk in HT-29 cells. Results showed that protein content in MFGM of yak milk is the highest among five MFGM. All MFGMs reduced cellular viability which was in agreement with cell morphology and apoptosis. However, the number of cells in S-phase from 24 h to 72 h was increased significantly by treatment with goat, buffalo and bovine MFGMs (100 μg/mL), but not yak and camel. All MFGMs treatment significantly reduced the mitochondrial membrane potential (with an order of goat > buffalo > bovine > camel > yak) and Bcl-2 expression, but increased the expression of both Bax and Caspase-3. Taken together, the results indicate that all MFGMs, especially goat and buffalo MFGMs, showed better effects at inducing apoptosis and reduction the viability of HT-29 cells. The mechanism might be arresting the cell cycle at S phase, depolarization of mitochondrial membrane potential, down-regulation of Bcl-2 expression and increase of Bax and Caspase-3 expression.
牛乳脂肪球膜(MFGM)具有多种健康益处,但对非牛 MFGM 的研究还不多。本研究旨在比较牛、山羊、水牛、牦牛和骆驼乳 MFGM 的抗增殖作用,并探讨其作用机制。结果表明,在五种 MFGM 中,牦牛乳 MFGM 的蛋白质含量最高。所有 MFGM 均降低了细胞活力,这与细胞形态和细胞凋亡一致。然而,用山羊、水牛和牛 MFGM(100μg/ml)处理可使细胞在 S 期的数量从 24 小时到 72 小时显著增加,但牦牛和骆驼 MFGM 则不然。所有 MFGM 处理均显著降低了线粒体膜电位(山羊>水牛>牛>骆驼>牦牛)和 Bcl-2 表达,但增加了 Bax 和 Caspase-3 的表达。综上所述,结果表明,所有 MFGM,特别是山羊和水牛 MFGM,在诱导 HT-29 细胞凋亡和降低细胞活力方面表现出更好的效果。其机制可能是将细胞周期阻滞在 S 期,线粒体膜电位去极化,下调 Bcl-2 表达,增加 Bax 和 Caspase-3 的表达。