食品科学 ›› 2019, Vol. 40 ›› Issue (13): 208-215.doi: 10.7506/spkx1002-6630-20180328-374

• 营养卫生 • 上一篇    下一篇

蓝莓花色苷提取物对人脂肪干细胞增殖、分化和脂质积累的影响

陈晓彤,马思思,郑婷婷,陈 洁,李亚丽,邓远乐,何 方,阴文娅   

  1. 1.四川大学华西公共卫生学院,四川 成都 610041;2.德阳市人民医院,四川 德阳 618000;3.四川大学华西医院甲状腺乳腺外科,四川 成都 610041
  • 出版日期:2019-07-15 发布日期:2019-07-23

Effect of Blueberry Anthocyanin Extract on Proliferation, Differentiation, and Lipid Accumulation in Human Adipose-Derived Stem Cells

CHEN Xiaotong, MA Sisi, ZHENG Tingting, CHEN Jie, LI Yali, DENG Yuanle, HE Fang, YIN Wenya   

  1. 1. West China School of Public Health, Sichuan University, Chengdu 610041, China; 2. People’s Hospital of Deyang City, Deyang 618000, China; 3. Department of Thyroid and Breast Surgery, West China Hospital, Sichuan University, Chengdu 610041, China
  • Online:2019-07-15 Published:2019-07-23

摘要: 目的:研究蓝莓花色苷提取物对人脂肪干细胞增殖、分化和功能的影响,评估其抗脂肪形成的能力及可能的机制。方法:原代分离培养人脂肪间充质干细胞,建立人脂肪细胞体外分化模型。采用不同质量浓度的蓝莓花色苷提取物干预不同生长时期的脂肪细胞。通过噻唑蓝法和乳酸脱氢酶测定,观察蓝莓花色苷提取物对脂肪细胞的增殖抑制作用。采用油红O染色实验和AdipoRed实验评价分化期脂肪细胞的脂质积累情况,采用葡萄糖氧化酶法测定成熟期脂肪细胞的葡萄糖吸收情况,采用酶联免疫吸附测定实验和实时荧光定量聚合酶链式反应法分析脂肪细胞因子分泌水平以及脂肪细胞成脂分化基因和脂肪细胞因子基因的表达量。结果:1)干预48 h后,蓝莓花色苷提取物可以显著抑制对数生长期、融合期的脂肪细胞增殖(P<0.05),且有剂量-效应关系(25~175 μg/mL);对分化期的脂肪细胞增殖也有显著抑制作用(P<0.05);同时极显著抑制成熟脂肪细胞的脂质积累(P<0.01)。2)不论1 μmol/L胰岛素是否存在,蓝莓花色苷提取物对成熟脂肪细胞的葡萄糖摄取均有显著的促进作用(P<0.05),且能够显著上调脂联素的表达(P<0.05)。3)蓝莓提取物使分化期脂肪细胞中的过氧化物酶体增殖物激活受体γ(peroxisome proliferator-activated receptor γ,PPARγ)表达下调,但在成熟期脂肪细胞中表达显著上调(P<0.05)。蓝莓花色苷提取物可以降低人脂肪干细胞的增殖,抑制细胞分化,减少脂质堆积。通过增加葡萄糖摄取以及脂联素和PPARγ的表达来维持或增强成熟脂肪细胞的功能。结论:蓝莓花色苷提取物可能具有抗肥胖的潜能。

关键词: 蓝莓, 花色苷, 人脂肪干细胞, 分化, 增殖, 肥胖

Abstract: Objective: This study was conducted to investigate the potential of blueberry extract to alter the growth, differentiation, and function of human adipose-derived stem cells (hADSCs) and to evaluate its ability of reducing adipose tissue formation and the possible underlying mechanisms. Methods: Human adipose-derived mesenchymal stem cells were isolated and primarily cultured to establish a model cell differentiation in vitro. Blueberry anthocyanin extract at different concentrations was used to intervene in different growth phase of adipocytes. The 3-(4,5-dimethyl-2-thiazolyl)- 2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay and the lactate dehydrogenase assay were measured to observe hADSC proliferation in different phases. Oil Red O staining and the AdipoRed assay were used to investigate lipid accumulation in hADCSs during the course of differentiation. The glucose uptake assay was used to investigate glucose uptake in fully differentiated mature human adipocytes. Enzyme-linked immunosorbent assay and real-time polymerase chain reaction were used to measure the expression of adipogenesis-related genes and the secretion of adipocytokines. Results: 1) Treatment with blueberry anthocyanins extract (25–175 μg/mL) for 48 h dose-dependently inhibited hADSCs proliferation in the logarithmic and confluent phases of growth (P < 0.05). It also inhibited hADSCs proliferation in the differentiation phase (P < 0.05), and lipid accumulation in mature adipocytes (P < 0.01). 2) The blueberry extract increased glucose uptake in mature adipocytes in both the absence and presence of 1 μmol/L insulin, and significantly up-regulated the expression of adiponectin (P < 0.05). 3) Peroxisome proliferator-activated receptor γ (PPARγ) expression in differentiating adipocytes was down-regulated by the blueberry extract during differentiation, while it was up-regulated in mature adipocytes (P < 0.05). These results suggest that the blueberry extract can reduce the proliferation and inhibit the differentiation of hADSCs to generate fewer mature adipocytes and less lipid accumulation. Furthermore, the blueberry extract also can maintain or enhance the function of human mature adipocytes by increasing glucose uptake and upregulating the expression of adiponectin and PPARγ. Conclusion: Blueberry anthocyanin extract may have the potential to inhibit obesity.

Key words: blueberry, anthocyanin, human adipose-derived stem cells, differentiation, proliferation, obesity

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