Unidad de Metabolismo Mineral, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Hospital Universitario Reina Sofía, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain.
Departamento de Genética, Universidad de Córdoba, Campus Rabanales, 14071 Córdoba, Spain.
J Nutr Biochem. 2016 Jun;32:151-62. doi: 10.1016/j.jnutbio.2016.03.005. Epub 2016 Mar 30.
Natural phenols may have beneficial properties against oxidative stress, which is associated with aging and major chronic aging-related diseases, such as loss of bone mineral mass (osteoporosis) and diabetes. The main aim of this study was to analyze the effect of quercetin, a major nutraceutical compound present in the "Mediterranean diet", on mesenchymal stem-cell (MSC) differentiation. Such cells were induced to differentiate into osteoblasts or adipocytes in the presence of two quercetin concentrations (0.1 and 10μM). Several physiological parameters and the expression of osteoblastogenesis and adipogenesis marker genes were monitored. Quercetin (10μM) inhibited cell proliferation, alkaline phosphatase (ALPL) activity and mineralization, down-regulating the expression of ALPL, collagen type I alpha 1 (COL1A1) and osteocalcin [bone gamma-carboxyglutamate protein (BGLAP)] osteoblastogenesis-related genes in MSC differentiating into osteoblasts. Moreover, in these cultures, CCAAT/enhancer-binding protein alpha (CEBPA) and peroxisome proliferator-activated receptor gamma 2 (PPARG2) adipogenic genes were induced, and cells differentiated into adipocytes were observed. Quercetin did not affect proliferation, but increased adipogenesis, mainly at 10-μM concentration in MSC induced to differentiate to adipocytes. β- and γ-catenin (plakoglobin) nuclear levels were reduced and increased, respectively, in quercetin-treated cultures. This suggests that the effect of high concentration of quercetin on MSC osteoblastic and adipogenic differentiation is mediated via Wnt/β-catenin inhibition. In conclusion, quercetin supplementation inhibited osteoblastic differentiation and promoted adipogenesis at the highest tested concentration. Such possible adverse effects of high quercetin concentrations should be taken into account in nutraceutical or pharmaceutical strategies using such flavonol.
天然酚类物质可能具有抗氧化应激的有益特性,而氧化应激与衰老和与衰老相关的主要慢性疾病有关,如骨矿物质丢失(骨质疏松症)和糖尿病。本研究的主要目的是分析槲皮素(一种存在于“地中海饮食”中的主要营养化合物)对间充质干细胞(MSC)分化的影响。在两种槲皮素浓度(0.1 和 10μM)存在的情况下,将这些细胞诱导分化为成骨细胞或脂肪细胞。监测了几种生理参数以及成骨细胞和脂肪细胞分化标记基因的表达。槲皮素(10μM)抑制细胞增殖、碱性磷酸酶(ALPL)活性和矿化,下调 MSC 向成骨细胞分化过程中成骨细胞相关基因 ALPL、I 型胶原α 1(COL1A1)和骨钙素[骨γ-羧基谷氨酸蛋白(BGLAP)]的表达。此外,在这些培养物中,CCAAT/增强子结合蛋白α(CEBPA)和过氧化物酶体增殖物激活受体γ 2(PPARG2)脂肪生成基因被诱导,并观察到细胞分化为脂肪细胞。槲皮素不影响增殖,但在 MSC 诱导分化为脂肪细胞时,在 10μM 浓度下增加脂肪生成。β-和γ-连环蛋白(斑联蛋白)核水平分别减少和增加。这表明高浓度槲皮素对 MSC 成骨和脂肪生成分化的影响是通过 Wnt/β-连环蛋白抑制介导的。总之,槲皮素补充抑制成骨细胞分化并在最高测试浓度下促进脂肪生成。在使用这种类黄酮的营养或药物策略中,应考虑高浓度槲皮素可能产生的这种不利影响。