Laboratório de Biotecnologia de Polímeros Naturais (BIOPOL), Departamento de Bioquímica, Centro de Biociências, Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte-RN, Brazil.
Laboratório de Biotecnologia de Polímeros Naturais (BIOPOL), Departamento de Bioquímica, Centro de Biociências, Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte-RN, Brazil; Disciplina de Biologia Molecular, Universidade Federal de São Paulo, São Paulo-SP, Brazil.
Int J Biol Macromol. 2018 May;111:1067-1075. doi: 10.1016/j.ijbiomac.2018.01.119. Epub 2018 Feb 19.
A low-molecular-weight (LMW) heterofucan (designated fucan B) was obtained from the brown seaweed, Spatoglossum schröederi, and its activity as an inhibitor of capillary-like tube formation by endothelial cells (ECs) was analyzed. Chemical, infrared and electrophoretic analyses confirmed the identity of fucan B. In contrast to other LMW fucans, fucan B (0.012-0.1 mg/mL) inhibited ECs capillary-like tube formation in a concentration-dependent manner. In addition, fucan B (0.01-0.05 mg/mL) did not affect ECs proliferation. Fucan B also inhibited ECs migration on a fibronectin-coated surface, but not on laminin- or collagen-coated surfaces. Biotinylated fucan B was used as a probe to identify its localization. Confocal microscopy experiments revealed that biotinylated fucan did not bind to the cell surface, but rather only to fibronectin. Our findings suggest that fucan B inhibits ECs capillary-like tube formation and migration by binding directly to fibronectin and blocking fibronectin sites recognized by cell surface ligands. However, further studies are needed to evaluate the in vivo effects of fucan B.
从褐藻 S. schröederi 中获得了一种低分子量(LMW)杂多糖(命名为 fucan B),并分析了其作为内皮细胞(EC)毛细血管样管形成抑制剂的活性。化学、红外和电泳分析证实了 fucan B 的身份。与其他 LMW 岩藻聚糖不同,fucan B(0.012-0.1mg/mL)以浓度依赖性方式抑制 EC 毛细血管样管形成。此外,fucan B(0.01-0.05mg/mL)不影响 ECs 的增殖。Fucan B 还抑制了纤维连接蛋白包被表面上的 EC 迁移,但不抑制层粘连蛋白或胶原蛋白包被表面上的迁移。生物素化 fucan B 被用作探针来鉴定其定位。共聚焦显微镜实验表明,生物素化 fucan 不与细胞表面结合,而仅与纤维连接蛋白结合。我们的研究结果表明,fucan B 通过与纤维连接蛋白直接结合并阻断细胞表面配体识别的纤维连接蛋白结合位点,抑制 ECs 毛细血管样管形成和迁移。然而,需要进一步研究来评估 fucan B 的体内作用。