Instituto Maimonides de Investigación Biomedica (IMIBIC). Hospital Universitario Reina Sofía de Córdoba, Universidad de Córdoba, 14004, Córdoba, Spain.
Genes Nutr. 2014 Jan;9(1):375. doi: 10.1007/s12263-013-0375-1. Epub 2013 Dec 14.
Metabolites derived from the polyunsaturated fatty acids (PUFA) may modulate the mesenchymal stromal cell (MSC) differentiation. Such cells can differentiate into different cellular types, including adipocytes and osteoblasts. Aging favors the bone marrow MSC differentiation toward the former, causing a loss of bone density associated with pathologies like osteoporosis. The omega-6 arachidonic acid (AA) favors MSC adipogenesis to a greater extent than omega-3 eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). In this work, we study the joint action of both PUFA. Thus, not induced and induced to adipocyte or osteoblast MSC were treated with 20 μM of each PUFA (either AA, AA + DHA or AA + EPA). The expression of osteogenic and adipogenic molecular markers, the alox15b lipoxygenase gene expression and the 5-, 8-, 11-, 12- and 15-hydroxyeicosatetraenoic acids (HETE) derived from the AA metabolism in the culture media were determined. The results show that the adipogenesis induction of AA is not suppressed by the joint presence of EPA and DHA. In fact, both increased the adipogenic effect of AA on MSC differentiated into osteoblasts. The different HETE concentrations increased in cultures supplemented with AA, albeit such concentrations were lower in the cultures induced to differentiate, mainly at day 21 after the induction. Furthermore, the reduction in the HETE concentration was correlated with a higher expression of the alox15b gene. These results highlight the PUFA metabolism differences between uninduced and induced MSC to differentiate into adipocytes and osteoblasts, besides the relevant role of the lipoxygenase gene expression in adipogenesis induction.
多不饱和脂肪酸(PUFA)衍生的代谢产物可能调节间充质基质细胞(MSC)的分化。这些细胞可以分化为不同的细胞类型,包括脂肪细胞和成骨细胞。衰老有利于骨髓 MSC 向前者分化,导致与骨质疏松症等疾病相关的骨密度丧失。与 ω-3 二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)相比,ω-6 花生四烯酸(AA)更有利于 MSC 脂肪生成。在这项工作中,我们研究了这两种 PUFA 的联合作用。因此,未诱导和诱导为脂肪细胞或成骨细胞的 MSC 分别用 20 μM 的每种 PUFA(AA、AA+DHA 或 AA+EPA)处理。测定了成骨和脂肪生成分子标志物的表达、阿洛 15b 脂加氧酶基因的表达以及培养基中 AA 代谢产生的 5-、8-、11-、12-和 15-羟基二十碳四烯酸(HETE)。结果表明,EPA 和 DHA 的共同存在并不能抑制 AA 的脂肪生成诱导。事实上,两者都增加了 AA 对分化为成骨细胞的 MSC 的脂肪生成作用。补充 AA 的培养物中不同的 HETE 浓度增加,尽管在诱导分化的培养物中,这种浓度较低,主要在诱导后第 21 天。此外,HETE 浓度的降低与 alox15b 基因的高表达相关。这些结果突出了未诱导和诱导 MSC 分化为脂肪细胞和成骨细胞之间的 PUFA 代谢差异,以及脂加氧酶基因表达在脂肪生成诱导中的相关作用。