Zhao Shancheng, Wang Zhen, Chen Jingxiao, Chen Jinghua
School of Pharmaceutical Science, Jiangnan University, Wuxi 214122, PR China.
School of Pharmaceutical Science, Jiangnan University, Wuxi 214122, PR China; Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122, PR China.
Carbohydr Res. 2015 Jan 12;401:32-8. doi: 10.1016/j.carres.2014.10.019. Epub 2014 Oct 29.
Heparan sulfate is a component of the extracellular matrix (ECM) that modulates individual development and cell growth through its interaction with growth factors. Structurally, heparan sulfate consists of repeating linear sulfated poly-anionic disaccharide structures. The K5 polysaccharide has the same structure as heparosan, and is the capsular polysaccharide of Escherichia coli K5 strain which serves as a precursor in heparin and heparan sulfate biosynthesis. Here, we prepared sulfated K5 polysaccharides that are structurally similar to heparan sulfate and investigated their biocompatibility and bioactivity in stem cell chondrogenic differentiation. Briefly, sulfation groups were added to -NH- and/or -OH of a precursor heparosan and the modified heparosan was qualitatively analyzed by FT-IR, (1)H NMR, and (13)C NMR techniques. Cell viability was not significantly affected by the sulfated K5 capsular polysaccharide. Relative mRNA expression of the chondrogenic differentiation marker COL2A1 was significantly upregulated in cells treated with the N,O-sulfated K5 polysaccharide confirming that the sulfated K5 capsular polysaccharide is able to stimulate chondrogenic differentiation. The main sulfation pattern for chondrogenic activity is N,6-O sulfation and the activity was not proportional to the sulfation level. This type of mimic was prepared in nearly a gram scale, supporting further structural study and 3 dimension stem cell culture. Together, the results of this study show that sulfated K5 capsular polysaccharides are able to stimulate chondrogenic differentiation without affecting cell viability.
硫酸乙酰肝素是细胞外基质(ECM)的一个组成部分,它通过与生长因子相互作用来调节个体发育和细胞生长。从结构上看,硫酸乙酰肝素由重复的线性硫酸化聚阴离子二糖结构组成。K5多糖与乙酰肝素具有相同的结构,是大肠杆菌K5菌株的荚膜多糖,在肝素和硫酸乙酰肝素生物合成中作为前体。在此,我们制备了结构与硫酸乙酰肝素相似的硫酸化K5多糖,并研究了它们在干细胞软骨生成分化中的生物相容性和生物活性。简而言之,将硫酸化基团添加到前体乙酰肝素的-NH-和/或-OH上,并通过傅里叶变换红外光谱(FT-IR)、氢核磁共振(1H NMR)和碳核磁共振(13C NMR)技术对修饰后的乙酰肝素进行定性分析。硫酸化K5荚膜多糖对细胞活力没有显著影响。在用N,O-硫酸化K5多糖处理的细胞中,软骨生成分化标志物COL2A1的相对mRNA表达显著上调,证实硫酸化K5荚膜多糖能够刺激软骨生成分化。软骨生成活性的主要硫酸化模式是N,6-O硫酸化,且活性与硫酸化水平不成正比。这种模拟物的制备规模接近一克,为进一步的结构研究和三维干细胞培养提供了支持。总之,本研究结果表明,硫酸化K5荚膜多糖能够刺激软骨生成分化而不影响细胞活力。