Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
Laboratory for Marine Drugs and Bioproducts of Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China.
Molecules. 2019 Jan 17;24(2):322. doi: 10.3390/molecules24020322.
Recently, sp., a kind of filamentous microalgae, has been studied for biofuel production due to its accumulation of triacylglycerols. However, the polysaccharides of sp. and their biological activities have rarely been reported. In this paper, we extracted sulfated polysaccharides from sp. (TSP), characterized their chemical composition and structure, and determined their immunostimulation and anticancer activities on RAW264.7 macrophage cells and HepG2 cells. The results showed that TSP is a sulfated polysaccharide with a M of 197 kDa. TSP is a heteropolysaccharide that is composed mainly of galactose. It showed significant immune-modulatory activity by stimulating macrophage cells, such as upregulating interleukin 6 (IL-6), interleukin 10 (IL-10), and tumor necrosis factor α (TNF-α). In addition, TSP also showed significant dose-dependent anticancer activity (with an inhibition rate of up to 66.8% at 250 µg/mL) on HepG2 cells as determined by the 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The cycle analysis indicated that the anticancer activity of TSP is mainly the result of induced cell apoptosis rather than affecting the cell cycle and mitosis of HepG2 cells. These findings suggest that TSP might have potential as an anticancer resource, but further research is needed, especially in vivo experiments, to explore the anticancer mechanism of TSP.
最近,由于积累了三酰基甘油,一种丝状微藻 sp. 被研究用于生产生物燃料。然而,sp. 的多糖及其生物活性很少有报道。在本文中,我们从 sp. 中提取了硫酸化多糖(TSP),对其化学组成和结构进行了表征,并确定了其对 RAW264.7 巨噬细胞和 HepG2 细胞的免疫刺激和抗癌活性。结果表明,TSP 是一种分子量为 197 kDa 的硫酸化多糖。TSP 是一种杂多糖,主要由半乳糖组成。它通过刺激巨噬细胞表现出显著的免疫调节活性,如上调白细胞介素 6(IL-6)、白细胞介素 10(IL-10)和肿瘤坏死因子 α(TNF-α)。此外,TSP 还对 HepG2 细胞表现出显著的剂量依赖性抗癌活性(在 250 µg/mL 时抑制率高达 66.8%),这是通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法确定的。细胞周期分析表明,TSP 的抗癌活性主要是诱导细胞凋亡的结果,而不是影响 HepG2 细胞的细胞周期和有丝分裂。这些发现表明,TSP 可能具有作为抗癌资源的潜力,但需要进一步研究,特别是体内实验,以探索 TSP 的抗癌机制。