Tao Yuheng, Ma Junmei, Huang Caoxing, Lai Chenhuan, Ling Zhe, Yong Qiang
Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing 210037, People's Republic of China; Key Laboratory of Forestry Genetics & Biotechnology of the Ministry of Education, Nanjing Forestry University, Nanjing 210037, People's Republic of China.
Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing 210037, People's Republic of China.
Int J Biol Macromol. 2022 Apr 30;205:530-538. doi: 10.1016/j.ijbiomac.2022.02.122. Epub 2022 Feb 22.
Galactomannan (GM) is widely recognized as an immune enhancer; however, the underlying molecular mechanism is still unknown. Herein, four products with molecular weights in descending order, namely GM40, GM50, GM65, and GMOS, were separated from incomplete degradation products of Sesbania cannabina GM by ethanol precipitation, followed by their immunomodulatory activity. Through FTIR and XPS spectra, the amount of free hydroxyl groups was shown to decrease in the following order: GM > GM50 > GMOS > GM40 > GM65. Moreover, the immunomodulatory activity of different products decreased in abovementioned order. The TNF-α, IL-6 and TLR4 content in RAW 264.7 cells treated with different GM products in the presence or absence of TAK-242 (TLR4 inhibitor) suggested that the immunomodulatory activity of GM and its degradation products is TLR4-dependent. Overall, the preliminary relationship indicated here between the hydroxyl groups or the possible deeper structural changes of GM and the immunomodulatory activity need to be further investigated.
半乳甘露聚糖(GM)被广泛认为是一种免疫增强剂;然而,其潜在的分子机制仍然未知。在此,通过乙醇沉淀从田菁GM的不完全降解产物中分离出四种分子量依次递减的产物,即GM40、GM50、GM65和GMOS,随后对它们的免疫调节活性进行了研究。通过傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)分析表明,游离羟基的数量按以下顺序减少:GM>GM50>GMOS>GM40>GM65。此外,不同产物的免疫调节活性也按上述顺序降低。在存在或不存在TAK-242(TLR4抑制剂)的情况下,用不同GM产物处理的RAW 264.7细胞中的肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和Toll样受体4(TLR4)含量表明,GM及其降解产物的免疫调节活性是TLR4依赖性的。总体而言,这里所表明的GM羟基基团之间的初步关系或可能更深层次的结构变化与免疫调节活性之间的关系仍需进一步研究。